Structure and functions of cell, transport across cell membrane, cell division, cell junctions. General principles of cell communication, the smallest unit that can live on its own and that makes up all living organisms and the tissues of the body The basic tenets of the cell theory are as follows: All living things are made up of one or more cells. The cell is the structural and functional unit of all living things. Cells come from pre-existing cells through the process of division. All cells are the same in regard to chemical composition. Cells also communicate with each other. Whether in plants, humans, or animals, they connect to create a solid, well formed organism. In humans, cells build tissues, tissues form organs, and organs work together to keep the body alive. Experts estimate that there are around 200Trusted Source cell types in the human body.

1. CELL
PRESENTED BY : JAGRUTI MARATHE

2. What is Cell
Cell Theory
Cell Theory
Timeline

3. WHAT IS CELL
• the smallest unit that can live on its
own and that makes up all living
organisms and the tissues of the body

4. CELL THEORY
• The basic tenets of the cell theory are as follows:
• All living things are made up of one or more cells.
• The cell is the structural and functional unit of all
living things.
• Cells come from pre-existing cells through the
process of division.
• All cells are the same in regard to chemical
composition.

8. WHAT IS A CELL?
cells as tiny packages that contain minute factories,
warehouses, transport systems, and power plants. They
function on their own, creating their own energy and self-
replicating — the cell is the smallest unit of life that can
replicate. Cells are the basic units of life.

9. WHAT IS A CELL?
Cells also communicate with each other. Whether in
plants, humans, or animals, they connect to create a
solid, well formed organism. In humans, cells build
tissues, tissues form organs, and organs work together
to keep the body alive.
Experts estimate that there are around 200Trusted
Source cell types in the human body.

10. WHAT IS A CELL?
Cell types can look different, and carry out distinct roles
within the body.
For instance, a sperm cell resembles a tadpole, a female
egg cell is spherical, and nerve cells are essentially thin
tubes.
Despite their differences, cells often share certain
structures. These are known as organelles or mini-
organs. Below are some of the most important:

11. PLASMA MEMBRANE
Plasma membrane
To ensure each cell remains separate from its neighbour, a
special membrane, known as the plasma membrane,
envelops the cell. Phospholipids make most of this
membrane and prevent water-based substances from
entering the cell. The plasma membrane contains a range
of receptors, which carry out a number of tasks, including
being:

12. PLASMA MEMBRANE
Gatekeepers: Some receptors allow certain molecules
through and stop others.
Markers: These receptors act as name badges, informing
the immune system that they are part of the organism and
not foreign invaders.
Communicators: Some receptors help the cell
communicate with other cells and the environment.
Fasteners: Some receptors help bind the cell to its
neighbours.

13. • The plasma membrane, a flexible yet sturdy barrier that surrounds
• and contains the cytoplasm of a cell, is best described by using a structural model called the
fluid mosaic model.
• According to this model , the molecular arrangement of the plasma membrane resembles a
• continually moving sea of fluid lipids that contains a mosaic of many different proteins Some
proteins float freely like icebergs in the lipid sea, whereas others are anchored at specific
locations like islands.
• The membrane lipids allow passage of several types of lipid soluble molecules but act as a
barrier to the entry or exit of charged or polar substances. Some of the proteins in the plasma
membrane allow
• movement of polar molecules and ions into and out of the cell.
• Other proteins can act as signal receptors or as molecules that link the plasma membrane to
intracellular or extracellular proteins.

15. Structure of the Plasma Membrane
• The Lipid Bilayer The basic structural framework of the plasma membrane is the lipid bilayer,
two back-to-back layers made up of three types of lipid molecules—phospholipids, cholesterol,
and glycolipids About 75% of the membrane lipids are phospholipids, lipids that contain
phosphorus.
• Present in smaller amounts are cholesterol (about 20%), a steroid with an attached
-OH (hydroxyl) group, and various glycolipids (about 5%), lipids with
attached carbohydrate groups.
• The bilayer arrangement occurs because the lipids are amphipathic molecules, which means
that they have both polar and nonpolar parts.
• In phospholipids , the polar part is the phosphate-containing “head,” which is hydrophilic
(hydro- = water; -philic = loving).
• The nonpolar parts are the two long fatty acid “tails,” which are hydrophobic (-phobic = fearing)
hydrocarbon chains.

16. • Because “like seeks like,” the phospholipid molecules orient themselves in the bilayer with their
hydrophilic heads facing outward.
• In this way, the heads face a watery fluid on either side— cytosol on the inside and extracellular
fluid on the outside.
• The hydrophobic fatty acid tails in each half of the bilayer point toward one another, forming a
nonpolar, hydrophobic region in the membrane’s interior.
• Cholesterol molecules are weakly amphipathic and are interspersed among the other lipids in
both layers of the membrane.
• The tiny -OH group is the only polar region of cholesterol, and it forms hydrogen bonds with the
polar heads of phospholipids and glycolipids.
• The stiff steroid rings and hydrocarbon tail of cholesterol are nonpolar; they fit among the fatty
acid tails of the phospholipids and glycolipids.
• The carbohydrate groups of glycolipids form a polar “head”; their fatty acid “tails” are nonpolar.
• Glycolipids appear only in the membrane layer that faces the extracellular fluid, which is one
reason the two sides of the bilayer are asymmetric, or different.

17. ARRANGEMENT OF
MEMBRANE PROTEINS
Membrane proteins are classified as integral or
peripheral according to whether they are firmly
embedded in the membrane.
Integral proteins (glycoproteins)
transmembrane proteins
peripheral proteins

18. Functions of Membrane Proteins

19. TRANSPORT ACROSS THE PLASMA MEMBRANE
• Transport of materials across the plasma membrane is essential to the life of a cell.
• Certain substances must move into the cell to support metabolic reactions.
• Other substances that have been produced by the cell for export or as cellular waste
products must move out of the cell.
• Substances generally move across cellular membranes via transport processes that can be
classified as passive or active, depending on whether they require cellular energy. In
passive processes, a substance moves down its concentration or electrical gradient to
cross the membrane using only its own kinetic energy (energy of motion).
• Kinetic energy is intrinsic to the particles that are moving.
• There is no input of energy from the cell. An example is simple diffusion.
• In active processes, cellular energy is used to drive the substance “uphill”
• against its concentration or electrical gradient.
• The cellular energy used is usually in the form of adenosine triphosphate (ATP).
• An example is active transport.
• Another way that some substances may enter and leave cells is an active process in
which tiny, spherical membrane sacs referred to as vesicles are used. Examples include
endocytosis, in which vesicles detach from the plasma membrane while bringing
materials into a cell, and exocytosis, the merging of vesicles with the
• plasma membrane to release materials from the cell.

20. Passive Processes
• The Principle of Diffusion: Diffusion (di-FŪ-zhun;
diffus- = spreading) is a passive process in which
the random mixing of particles in a solution
occurs because of the particles’ kinetic energy.
Both the solutes, the dissolved substances, and
the solvent, the liquid that does the dissolving,
undergo diffusion.
• diffuse toward the area of lower
concentration—they move down their
concentration gradient.
• After some time, the particles become evenly
distributed throughout the solution and the
solution is said to be at equilibrium

21.  Several factors influence the diff usion rate of substances across plasma
membranes:
• Steepness of the concentration gradient. The greater the difference in
concentration between the two sides of the membrane, the higher the rate of
diffusion. When charged particles are diff using, the steepness of the
electrochemical gradient determines the diffusion rate
across the membrane.
• Temperature. The higher the temperature, the faster the rate of diffusion. All of
the body’s diffusion processes occur more rapidly in a person with a fever.
Facilitated Diffusion :Solutes that are too polar or highly charged to move through
the lipid bilayer by simple diffusion can cross the plasma membrane by a passive
process called facilitated diffusion. In this process, an integral membrane protein
assists a specific substance across the membrane. The integral membrane protein
can be either a membrane channel or a carrier.
CHANNEL-MEDIATED FACILITATED DIFFUSION In channel-mediated facilitated
diffusion, a solute moves down its concentration gradient across the lipid bilayer
through a membrane channel .

22. SIMPLE DIFFUSION
• Simple diffusion is a passive process in which substances move
freely through the lipid bilayer of the plasma membranes of cells
without the help of membrane transport proteins.
• Nonpolar, hydrophobic molecules move across the lipid bilayer
through the process of simple diffusion.
• Such molecules include oxygen, carbon dioxide, and nitrogen
gases; fatty acids; steroids; and fat-soluble vitamins (A, D, E,
and K).
• Small, uncharged polar molecules such as water, urea, and
small alcohols also pass through the lipid bilayer by simple
diffusion.

23. FACILITATED DIFFUSION
Facilitated Diffusion :Solutes that are too polar or highly
charged to move through the lipid bilayer by simple diffusion
can cross the plasma membrane by a passive process called
facilitated diffusion.
In this process, an integral membrane protein assists a specific
substance across the membrane.
The integral membrane protein can be either a membrane
channel or a carrier.

24. CHANNEL-MEDIATED
FACILITATED DIFFUSION
• In channel-mediated facilitated diffusion, a solute moves down its
concentration gradient across the lipid bilayer through a membrane
channel .
• Most membrane channels are ion channels, integral transmembrane
proteins that allow passage of small, inorganic ions that are too
hydrophilic to penetrate the nonpolar interior of the lipid bilayer.
• Each ion can diff use across the membrane only at certain sites.
• In typical plasma membranes, the most numerous ion channels are
selective for K+ (potassium ions) or Cl− (chloride ions); fewer channels
are available for Na+ (sodium ions) or Ca2+ (calcium ions).
• Diffusion of ions through channels is generally slower than free diffusion
through the lipid bilayer because channels occupy a smaller fraction of the
membrane’s total surface area than lipids.
• Still, facilitated diffusion through channels is a very fast process: More
than a million potassium ions can flow through a K+ channel in one
second!

25. • Channel-mediated facilitated diffusion of potassium ions (K+) through a gated K+
channel.
• A gated channel is one in which a portion of the channel protein acts as a gate to
open or close the channel’s pore to the passage of ions.
Channels are integral membrane proteins that allow specific, small, inorganic ions
to pass across the membrane by facilitated diffusion.

26. • A channel is said to be gated when part of the channel protein acts as a “plug”
or “gate,” changing shape in one way to open the pore and in another way to
close it .
• Some gated channels randomly alternate between the open and closed
positions; others are regulated by chemical or electrical changes inside and
outside the cell.
• When the gates of a channel are open, ions diff use into or out of cells, down
their electrochemical gradients.
• The plasma membranes of different types of cells may have different numbers
of ion channels and thus display different permeability's to various ions.

27. CARRIER-MEDIATED
FACILITATED DIFFUSION
• In carrier-mediated facilitated diffusion, a carrier (also called a
transporter) moves a solute down its concentration gradient across the
plasma membrane.
• Since this is a passive process, no cellular energy is required. The solute
binds to a specific carrier on one side of the membrane and is released on
the other side after the carrier undergoes a change in shape. The solute
binds more often to the carrier on the side of the membrane with a higher
concentration of solute.
• Once the concentration is the same on both sides of the membrane,
solute molecules bind to the carrier on the cytosolic side and move out to
the extracellular fluid as rapidly as they bind to the carrier on the
extracellular side and move into the cytosol.
• The rate of carrier-mediated facilitated diffusion (how quickly it occurs) is
determined by the steepness of the concentration gradient across the
membrane.
• The number of carriers available in a plasma membrane places an upper
limit, called the transport maximum, on the rate at which facilitated
diffusion can occur. Once all of the carriers are occupied, the

28. Carrier-mediated facilitated diffusion of glucose across a plasma membrane. The
carrier protein binds to glucose in the extracellular fluid and releases it into the cytosol.
Carriers are integral membrane proteins that undergo changes in shape in
order to move substances across the membrane by facilitated diffusion.

30. OSMOSIS
Osmosis is a type of diffusion in which there is net movement of a solvent through a selectively permeable
membrane.
Like the other types of diffusion, osmosis is a passive process. In living systems, the solvent is water, which
moves by
osmosis across plasma membranes from an area of higher water
concentration to an area of lower water concentration.

31. Principle of osmosis. Water molecules move through the selectively permeable
membrane; solute molecules cannot.
(a) Water molecules move from the left arm into the right arm, down the water
concentration gradient.
(b) The volume of water in the left arm has decreased and the volume of solution in the
right arm has increased.
(c) Pressure applied to the solution in the right arm restores the starting conditions.
Osmosis is the movement of water molecules through a selectively permeable membrane.

32. • A solution’s tonicity (to - -NIS-i-tē; tonic = tension) is a measure of the solution’s
ability to change the volume of cells by altering their water content.
Cells placed in an isotonic solution maintain their shape because there is no net water
movement into or out of the cells.

33. ACTIVE PROCESSES
• Active Transport Some polar or charged solutes that must enter or leave body cells
cannot cross the plasma membrane through any form of passive transport because they
would need to move “uphill,” against their concentration gradients.
• Such solutes may be able to cross the membrane by a process called active transport.
• Active transport is considered an active process because energy is required for carrier
proteins to move solutes across the membrane against a concentration gradient.
Two sources of cellular energy can be used to drive active transport:
(1) Energy obtained from hydrolysis of adenosine triphosphate (ATP) is the source in
primary active transport;
(2) energy stored in an ionic concentration gradient is the source in secondary active
transport.

34. ACTIVE TRANSPORT
PRIMARY ACTIVE TRANSPORT
Energy derived from hydrolysis of ATP changes the
shape of a carrier protein, which “pumps” a substance
across a plasma membrane against its concentration
gradient.
Indeed, carrier proteins that mediate primary active
transport are often called pumps.
40% of the ATP it generates on primary active
transport Chemicals that turn off ATP production—
for example, the poison cyanide—are lethal
because they shut down active transport in cells
throughout the body.
SECONDARY ACTIVE
TRANSPORT
Energy stored in a Na+ or H+ concentration gradient is
used to drive other substances across the membrane
against their own concentration gradients.
Because a Na+ or H+ gradient is established by
primary active transport, secondary active transport
indirectly uses energy obtained from the hydrolysis of
ATP.
The sodium–potassium pump maintains a steep
concentration gradient of Na+ across the plasma
membrane.

35. • The most prevalent primary active transport mechanism expels sodium ions (Na+) from cells
and brings potassium ions (K+) in.
• Because of the specific ions it moves, this carrier is called the sodium– potassium pump.
Because a part of the sodium–potassium pump acts as an ATPase, an enzyme that
hydrolyses ATP, another name for this pump is Na+–K+ ATPase.
• All cells have thousands of sodium– potassium pumps in their plasma membranes. These
sodium potassium pumps maintain a low concentration of Na+ in the cytosol by pumping
these ions into the extracellular fluid against the Na+ concentration gradient.
• At the same time, the pumps move K+ into cells against the K+ concentration gradient.
• Because K+ and Na+ slowly leak back across the plasma membrane down their
electrochemical gradients—through passive transport or secondary active transport—the
sodium–potassium pumps must work nonstop to maintain a low concentration of Na+ and a
high concentration of K+ in the cytosol.

36. 1 Three Na+ in the cytosol bind to the pump protein.
2 Binding of Na+ triggers the hydrolysis of ATP into ADP, a reaction that also attaches a phosphate group P to
the pump protein This chemical reaction changes the shape of the pump protein, expelling the three Na+ into the
extracellular fluid. Now the shape of the pump protein favors binding of two K+ in the extracellular
fluid to the pump protein.
3 The binding of K+ triggers release of the phosphate group from the pump protein. This reaction again causes
the shape of the pump protein to change.
4 As the pump protein reverts to its original shape, it releases K+ into the cytosol. At this point, the pump is
again ready to bind three Na+, and the cycle repeats.

37. • The sodium–potassium pump maintains a steep concentration gradient of Na+ across the
plasma membrane. As a result, the sodium ions have stored or potential energy.
• Accordingly, if there is a route for Na+ to leak back in, some of the stored energy can be
converted to kinetic energy (energy of motion) and used to transport other substances
against their concentration gradients.
• In essence, secondary active transport proteins harness the energy in the Na+ concentration
gradient by providing routes for Na+ to leak into cells.
• In secondary active transport, a carrier protein simultaneously binds to Na+ and another
substance and then changes its shape so that both substances cross the membrane at the
same time.
• If these transporters move two substances in the same direction they are called symporters
(sim-PORT-ers; sym- = same);
• antiporters (an′-tē-PORT-ers), by contrast, move two substances in opposite directions
across the membrane (anti- = against).

38. • Plasma membranes contain several antiporters and symporters that are powered
by the Na+ gradient .
• For instance, the concentration of calcium ions (Ca2+) is low in the cytosol
because Na+–Ca2+ antiporters eject calcium ions.
• Likewise, Na+–H+ antiporters help regulate the cytosol’s pH (H+ concentration)
by expelling excess H+.
• By contrast, dietary glucose and amino acids are absorbed into cells that line the
small intestine by Na+–glucose and Na+–amino acid symporters .
• In each case, sodium

39. TRANSPORT IN VESICLES
A vesicle :, is a small, spherical sac. , a variety of substances
are transported in vesicles from one structure to another within
cells. Vesicles also import materials from and release materials
into extracellular fluid.
During endocytosis (en′-do--sī-TO- -sis; endo- = within),
materials move into a cell in a vesicle formed from the plasma
membrane. In exocytosis (ek′-so--sī-TO- -sis; exo- = out),
materials move out of a cell by the fusion with the plasma
membrane of vesicles formed inside the cell.
Both endocytosis and exocytosis require energy supplied by
ATP. Thus, transport in vesicles is an active process.

40. ENDOCYTOSIS
Three types of endocytosis:
• Receptor-mediated endocytosis (is a highly selective type of endocytosis by
which cells take up specific ligands. Recall that ligands are molecules that bind to specific
receptors.)
• Phagocytosis (cell eating” is a form of endocytosis in which the cell engulfs large solid
particles, such as worn-out cells, whole bacteria, or viruses)
• and Bulk-phase endocytosis (also called pinocytosis “cell drinking,” a form of endocytosis in
which tiny droplets of extracellular fluid are taken up)

41. Binding. On the extracellular side of the plasma membrane, an LDL particle that
contains cholesterol binds to a specific receptor in the plasma membrane to form a
receptor–LDL complex. The receptors are integral membrane proteins that are
concentrated in regions of the plasma membrane called clathrin-coated pits. Here, a
protein called clathrin attaches to the membrane on its cytoplasmic side. Many clathrin
molecules come together, forming a basketlike structure around the receptor–LDL
complexes that causes the membrane to invaginate (fold inward).
2 Vesicle formation. The invaginated edges of the membrane around the clathrin-
coated pit fuse, and a small piece of the membrane pinches off . The resulting vesicle,
known as a clathrincoated vesicle, contains the receptor–LDL complexes.
3 Uncoating. Almost immediately aft er it is formed, the clathrincoated vesicle loses
its clathrin coat to become an uncoated vesicle. Clathrin molecules either return to the
inner surface
of the plasma membrane or help form coats on other vesicles inside the cell.
4 Fusion with endosome. The uncoated vesicle quickly fuses with a vesicle known
as an endosome. Within an endosome, the LDL particles separate from their
receptors.
5 Recycling of receptors to plasma membrane. Most of the receptors accumulate
in elongated protrusions of the endosome (the arms of the cross-shaped vesicle at the
center
of the figure). These pinch off , forming transport vesicles that return the receptors to
the plasma membrane. An LDL receptor is returned to the plasma membrane about 10
minutes aft er it enters a cell.
6 Degradation in lysosomes. Other transport vesicles, which contain the LDL
particles, bud off the endosome and soon fuse with a lysosome. Lysosomes contain
many digestive enzymes. Certain enzymes break down the large protein and lipid
molecules

42. PHAGOCYTOSIS
• “Cell eating” Only a few body cells, termed phagocytes ,
are able to carry out phagocytosis.
• Two main types of phagocytes are macrophages and
neutrophils
• Macrophages located in many body tissues, and
neutrophils, a type of white blood cell.
• Phagocytosis begins when the particle binds to a plasma
membrane receptor on the phagocyte, causing it to extend
pseudopods (SOO-do--pods; pseudo- = false; -pods =
feet), projections of its plasma membrane and cytoplasm

43. BULK PHAGOCYTOSIS
• “cell drinking,” form of endocytosis in which tiny droplets of
extracellular fluid are taken up .
• No receptor proteins are involved; all solutes dissolved in the
extracellular fluid are brought into the cell.
• During bulk-phase endocytosis, the plasma membrane folds inward
and forms a vesicle containing a droplet of extracellular fluid.
• The vesicle detaches or “pinches off ” from the plasma membrane
and enters the cytosol.
• Within the cell, the vesicle fuses with a lysosome, where enzymes
degrade the engulfed solutes. The resulting smaller molecules, such
as amino acids and fatty acids, leave the lysosome to be used
elsewhere in the cell.
• Bulk-phase endocytosis occurs in most cells, especially absorptive
cells in the intestines and kidneys.

44. EXOCYTOSIS
All cells carry out exocytosis, but it is especially important in two types of
cells:
(1) secretory cells that liberate digestive enzymes, hormones, mucus, or
other secretions
(2) nerve cells that release substances called neurotransmitters

45. CYTOPLASM
Cytoplasm
The cytoplasm is the interior of the cell that surrounds the
nucleus. It includes the organelles and a jelly-like fluid
called the cytosol. Many of the important reactions that
take place in the cell occur in the cytoplasm.
Cytoplasm consists of all the cellular contents between
the plasma
membrane and the nucleus, and has two components: (1)
the cytosol
and (2) organelles, tiny structures that perform different
functions in
the cell.

46. CYTOPLASM
The cytoplasm consists of all the cellular contents between the plasma membrane and the
nucleus.
This compartment has two components: cytosol and organelles.
Cytosol (SI--to - -sol), the fluid portion of cytoplasm, also called intracellular fluid, contains water,
dissolved solutes, and suspended particles.
Within the cytosol are several different types of organelles . cytoplasm
Each type of organelle has a characteristic shape and specific functions. Examples include the
cytoskeleton, ribosomes, endoplasmic reticulum, Golgi complex, lysosomes, peroxisomes, and
mitochondria.

47. CYTOSOL
• The cytosol (intracellular fluid) is the fluid portion of the cytoplasm
that surrounds organelles and constitutes about 55% of total cell volume.
• Although it varies in composition and consistency from one part of a cell to another, cytosol is
75–90% water plus various dissolved and suspended components.
• different types of ions, glucose, amino acids, fatty acids, proteins, lipids, ATP, and waste
products
• In some cells are various organic molecules that aggregate into masses for storage. These
aggregations may appear and disappear at different times in the life of a cell. Examples
include lipid droplets that contain triglycerides, and clusters of glycogen molecules called
glycogen granules

48. • The cytosol is the site of many chemical reactions required for a cell’s existence. For
example, enzymes in cytosol catalyze glycolysis, a series of 10 chemical reactions that
produce two molecules of ATP from one molecule of glucose
• Other types of cytosolic reactions provide the building blocks for maintenance of cell
structures and for cell growth.

49. CYTOSKELETON
The cytoskeleton forms the scaffolding within the cytoplasm of
the human cell. It helps the cell maintain the correct shape.
However, unlike regular scaffolding, the cytoskeleton is flexible.
It plays a role in cell division and cell motility — the ability of
some cells to move, such as sperm cells, for instance.
The cytoskeleton also helps with cell signalling through the
uptake of material from the endocytosis, or the area outside the
cell, and moving materials within the cell.
• The cytoskeleton is a network of protein filaments that
extends throughout the cytosol .
• Three types of filaments contribute to the cytoskeleton’s
structure, as well as the structure of other organelles.
• In the order of their increasing diameter, these structures
are microfilaments, intermediate filaments, and
microtubules.

50. They are composed of the proteins actin and myosin
and are most prevalent at the edge of a cell .
Microfilaments have two general functions: They help
generate movement and provide mechanical support.
Microvillus
Microfilaments
Nucleus
(a) Microfilament
(b) Intermediate filament
(c) Microtubule
Intermediate
filaments
Centrosome
Microtubules
Intermediate are thicker than microfilaments but thinner
than microtubules. Several different proteins can
compose intermediate filaments, which are exceptionally
strong.
They are found in parts of cells subject to mechanical
stress; they help stabilize the position of organelles such
as the nucleus and help attach cells toone another.
Microtubules the largest of the cytoskeletal
components, are long, unbranched hollow tubes
composed mainly of the protein tubulin. The
assembly of microtubules begins in an organelle
called the centrosome .
Microtubules help determine cell shape. They also
function in the movement of organelles such as
secretory vesicles, of chromosomes during cell
division, and of specialized cell projections,
such as cilia and flagella.

51. Functions of the Cytoskeleton:
1. Serves as a scaff old that helps determine a cell’s shape and organize
the cellular contents.
2. Aids movement of organelles within the cell, of chromosomes during
cell division, and of whole cells such as phagocytes.

52. NUCLEUS
The nucleus represents the cell’s headquarters. There is
typically one nucleus per cell. However, this is not always
the case. Skeletal muscle cells, for instance, have two.
The nucleus contains the majority of the cell’s DNA, and
the mitochondria house a small amount. The nucleus
sends out messages to tell the cell to grow, divide, or die.
A membrane called the nuclear envelope separates the
nucleus from the rest of the cell. Nuclear pores within the
membrane allow small molecules and ions to cross back
and forth, while larger molecules need to transport
proteins to help them through.

53. • The nucleus is a spherical or oval-shaped structure that usually is the
most prominent feature of a cell.
• Most cells have a single nucleus, although some, such as mature red
blood cells, have none.
• In contrast, skeletal muscle cells and a few other types of cells have
multiple nuclei.
• A double membrane called the nuclear envelope separates the nucleus
from the cytoplasm.
• Both layers of the nuclear envelope are lipid bilayers similar to the plasma
membrane.
• The outer membrane of the nuclear envelope is continuous with rough ER
and resembles it in structure.
• Many openings called nuclear pores extend through the nuclear
envelope.
• Each nuclear pore consists of a circular arrangement of proteins
surrounding a large central opening that is about 10 times wider than the
pore of a channel protein in the plasma membrane.

54. FUNCTIONS OF THE
NUCLEUS
1. Controls cellular structure.
2. Directs cellular activities.
3. Produces ribosomes in nucleoli.

55. • Nuclear pores control the movement of substances between the
nucleus and the cytoplasm.
• Small molecules and ions move through the pores passively by diffusion.
• Most large molecules, such as RNAs and proteins, cannot pass through
the nuclear pores by diffusion.
• Instead, their passage involves an active transport process in which the
molecules are recognized and selectively transported through the nuclear
pore into or out of the nucleus.
• For example, proteins needed for nuclear functions move from the cytosol
into the nucleus; newly formed RNA molecules move from the nucleus
into the cytosol in this
manner.

56. NUCLEOLUS
The nucleolus is the largest structure in the
nucleus of eukaryotic cells.
It is best known as the site of ribosome
biogenesis, which is the synthesis of ribosomes.
The nucleolus also participates in the formation
of signal recognition particles and plays a role in
the cell's response to stress.
Each nucleolus is simply a cluster of protein,
DNA, and
RNA; it is not enclosed by a membrane. Nucleoli
are the sites of
synthesis of rRNA and assembly of rRNA and
proteins into ribosomal subunits.

57. • Nucleoli disperse
and disappear during cell division and reorganize once new cells are formed.
• The cell’s hereditary units , called genes
Genes are arranged along chromosomes.
Human somatic (body) cells have 46 chromosomes, 23 inherited from each parent.
• Each chromosome is a long molecule of DNA that is coiled
together with several proteins
• This complex of DNA, proteins, and some RNA is called chromatin (KRO- -ma-tin).
• The total genetic information carried in a cell or an organism is its
genome

58. RIBOSOMES
Ribosomes
The nucleus transcribes segments of DNA into ribonucleic
acid (RNA), a molecule similar to DNA, which directs the
translation of RNA into proteins. Ribosomes read the RNA
and translate it into proteins by sticking together amino
acids in the order the RNA defines.
Some ribosomes float freely in the cytoplasm while others
attach to the ER.
Functions of Ribosomes
1. Ribosomes associated with endoplasmic reticulum
synthesize proteins
destined for insertion in the plasma membrane or secretion
from the cell.
2. Free ribosomes synthesize proteins used in the cytosol.

59. • Ribosomes are the sites of protein synthesis.
• The name of these tiny structures reflects their high content of one type of ribonucleic acid
(ribosomal RNA, or rRNA), but each ribosome also includes more than 50 proteins.
• Structurally, a ribosome consists of two subunits, one about half the size of the other
• The large and small subunits are made separately in the nucleolus, a spherical body inside the
nucleus.
• Once produced, the large and small subunits exit the nucleus separately, then come together
in the cytoplasm.

60. ENDOPLASMIC RETICULUM
Endoplasmic reticulum
The endoplasmic reticulum (ER) processes molecules within the
cell and helps transport them to their final destinations. In
particular, it synthesizes, folds, modifies, and transports proteins.
Cisternae are long sacs that make the ER. The cytoskeleton holds
them together. There are two ER types: rough ER and smooth ER.
Functions of Endoplasmic Reticulum
1. Rough ER synthesizes glycoproteins and phospholipids that are
transferred into cellular organelles, inserted into the plasma
membrane, or secreted during exocytosis.
2. Smooth ER synthesizes fatty acids and steroids, such as
estrogens and testosterone; inactivates or detoxifies drugs and
other potentially harmful substances; removes the phosphate
group from glucose-6-phosphate; and stores and releases calcium
ions that trigger contraction in muscle cells.

61. • The endoplasmic reticulum (ER) is a network of membranes in the form of flattened sacs or
tubules .
• The ER extends from the nuclear envelope (membrane around the nucleus), to which it is
connected and projects throughout the cytoplasm.
• The ER is so extensive that it constitutes more than half of the membranous surfaces within
the cytoplasm of most cells.
• Cells contain two distinct forms of ER, which differ in structure and function.

62. ROUGH ER
It is continuous with the nuclear membrane and usually is folded
into a series of flattened sacs.
The outer surface of rough ER is studded with ribosomes, the
sites of protein synthesis. Proteins synthesized by ribosomes
attached to rough ER enter spaces within the ER for processing
and sorting. In some cases, enzymes attach the proteins to
carbohydrates to form glycoproteins. In other cases, enzymes
attach the proteins to phospholipids, also synthesized by rough
ER.
These molecules (glycoproteins and phospholipids) may be
incorporated into the membranes of organelles, inserted into the
plasma membrane, or secreted via exocytosis. Thus rough ER
produces secretory proteins, membrane proteins, and many
organellar proteins.
SMOOTH ER
It extends from the rough ER to form a network of membrane
tubules . Unlike rough ER, smooth ER does not have ribosomes
on the outer surfaces of its membrane. However,
smooth ER contains unique enzymes that make it functionally
more diverse than rough ER. Because it lacks ribosomes,
smooth ER does not synthesize proteins, but it does synthesize
fatty acids and steroids, such as estrogens and testosterone. In
liver cells, enzymes of the smooth ER help release glucose into
the bloodstream and inactivate or detoxify lipid-soluble drugs or
potentially harmful substances, such as alcohol, pesticides, and
carcinogens (cancer-causing agents).
In liver, kidney, and intestinal cells, a smooth ER enzyme
removes the
phosphate group from glucose-6-phosphate, which allows the
“free” glucose to enter the bloodstream. In muscle cells, the
calcium ions(Ca2+) that trigger contraction are released from the
sarcoplasmic reticulum, a form of smooth ER.

63. GOLGI APPARATUS
Once the ER processes the molecules, they travel to the
Golgi apparatus. People tend to consider the Golgi
apparatus the post office of the cell, where items go
through packaging and labeling. Once materials leave,
they may be useful inside or outside the cell.
Functions of the Golgi Complex
1. Modifies, sorts, packages, and transports proteins
received from the rough ER.
2. Forms secretory vesicles that discharge processed
proteins via exocytosis into extracellular fluid; forms
membrane vesicles that ferry new molecules to the
plasma membrane; forms transport vesicles that carry
molecules to other organelles, such as lysosomes.

64. Processing and packaging of proteins by the Golgi complex.

65. MITOCHONDRIA
People may often refer to mitochondria as the
powerhouses of cells. They help turn energy from
food into energy that the cell can use — adenosine
triphosphate. However, mitochondria have a
number of other jobs, including calcium storage
and a role in cell death.
Functions of Mitochondria
1. Generate ATP through reactions of aerobic cellular
respiration.
2. Play an important early role in apoptosis.

66. MITOCHONDRIA
Mitochondria are often referred to as the powerhouses
of the cell. They help turn the energy we take from food
into energy that the cell can use. But, there is more to
mitochondria than energy production.
Present in nearly all types of human cell, mitochondria
are vital to our survival. They generate the majority of
our adenosine triphosphate (ATP), the energy currency
of the cell.
Mitochondria are also involved in other tasks, such as
signalling between cells and cell death, otherwise known
as apoptosis.

67. CELL DIVISION
cell division, the process by which
cells reproduce themselves.
• somatic cell division
• and reproductive cell division

68. CELL DIVISION
Diploid cells within the testes undergo meiosis to produce haploid sperm
cells with 23 chromosomes. A single diploid cell yields four haploid sperm
cells. They contain one complete set of 23 chromosomes.
In females, meiosis begins during the fetal stage, before the individual is
born. It happens in stages.
A series of diploid future egg cells enter meiosis. At the end of the first
stage of meiosis the process stops, and the cells gather in the ovaries.
At puberty, one female egg cell resumes meiosis each month. As meiosis
completes, it yields a single haploid egg cell each monthly cycle.
During human reproduction, the haploid sperm and haploid egg combine.
This temporarily doubles the number of chromosomes. A small portion of
each chromosome breaks off and reattaches to its partner chromosome
before fertilization finishes.

69. There are two types of cell division:
mitosis and meiosis. Most of the time when people refer to “cell division,” they mean mitosis, the
process of making new body cells.
Meiosis is the type of cell division that creates egg and sperm cells.
Mitosis is a fundamental process for life.
During mitosis, a cell duplicates all of its contents, including its chromosomes, and splits to form two
identical daughter cells.
Because this process is so critical, the steps of mitosis are carefully controlled by certain genes.
When mitosis is not regulated correctly, health problems such as cancer can result.
The other type of cell division, meiosis, ensures that humans have the same number of
chromosomes in each generation.
It is a two-step process that reduces the chromosome number by half—from 46 to 23—to form
sperm and egg cells.
When the sperm and egg cells unite at conception, each contributes 23 chromosomes so the
resulting embryo will have the usual 46.
Meiosis also allows genetic variation through a process of gene shuffling while the cells are dividing

70. SOMATIC CELL DIVISION
A somatic cell (so--MAT-ik; soma = body) is any cell of the body
other than a germ cell.
A germ cell is a gamete (sperm or oocyte) or any precursor cell
destined to become a gamete.
In somatic cell division, a cell undergoes a nuclear division
called mitosis (mī-TO - -sis; mitos = thread) and a
cytoplasmic division called cytokinesis (sī-to - - ki-NE--sis;
cyto- = cell; -kinesis = movement) to produce two genetically
identical cells, each with the same number and kind of
chromosomes as the original cell.
Somatic cell division replaces dead or injured cells and adds
new ones during tissue growth.

71. SOMATIC CELL DIVISION
A cell reproduces, it must replicate (duplicate) all its
chromosomes to pass its genes to the next generation of
cells. The cell cycle consists of two major periods:
• Interphase, when a cell is not dividing,
• and the Mitotic (M) phase, when a cell is dividing

72. INTERPHASE :
DURING INTERPHASE -THE CELL REPLICATES ITS DNA THROUGH A PROCESS THAT
WILL BE DESCRIBED SHORTLY. IT ALSO PRODUCES ADDITIONAL ORGANELLES AND
CYTOSOLIC COMPONENTS IN ANTICIPATION OF CELL DIVISION. INTERPHASE IS A
STATE OF HIGH METABOLIC ACTIVITY; IT IS DURING THIS TIME THAT THE CELL DOES
MOST OF ITS GROWING. INTERPHASE CONSISTS OF THREE PHASES: G1, S, AND G2
G1is the interval between the mitotic phase and the S phase. During G1, the cell
is metabolically active; it replicates most of its organelles and cytosolic
components but not its DNA. Replication of centrosomes also begins in the G1
phase. Virtually all of thecellular activities described in this chapter happen during
G1. For acell with a total cell cycle time of 24 hours, G1 lasts 8 to 10 hours.
However,the duration of this phase is quite variable. It is very short in many
embryonic cells or cancer cells. Cells that remain in G1 for a very long time,
perhaps destined never to divide again, are said to be in the G0 phase. Most
nerve cells are in the G0 phase.
Once a cell enters the S phase, however, it is committed to go through the rest of
the cell cycle. The S phase, the interval between G1 and G2, lasts about 8 hours.
During the S phase, DNA replication occurs. As a result of DNA replication, the
two identical cells formed during cell division later in the cell cycle will have the
same genetic material. The G2 phase is the interval between the S phase and
the mitotic phase. It lasts 4 to 6 hours.
During G2, cell growth continues, enzymes and other proteins are synthesized in
preparation for cell division, and replication of centrosomes is completed. When
DNA replicates during the S phase, its helical structure partially uncoils, and the
two strands separate at the points where hydrogen bonds connect base pairs

73. MITOTIC PHASE
The mitotic (M) phase of the cell cycle,
which
results in the formation of two identical
cells, consists of a nuclear
division (mitosis) and a cytoplasmic
division (cytokinesis) to form two
identical cells. The events that occur
during mitosis and cytokinesis
are plainly visible under a microscope
because chromatin condenses
into discrete chromosomes.

74. REPRODUCTIVE CELL DIVISION
• In the process called sexual reproduction, each new organism is the
result of the union of two different gametes (fertilization), one produced by
each parent.
• If gametes had the same number of chromosomes as somatic cells, the
number of chromosomes would double at fertilization.
• Meiosis (mī-O- -sis; mei- = lessening; -osis = condition of), the
reproductive cell division that occurs in the gonads (ovaries and testes),
produces gametes in which the number of chromosomes is reduced by
half.
• As a result, gametes contain a single set of 23 chromosomes and thus
are haploid (n) cells (HAP-loyd; hapl- = single).
• Fertilization restores the diploid number of chromosomes. Meiosis Unlike
mitosis, which is complete aft er a single round, meiosis occurs in two
successive stages:
 meiosis I
 and meiosis II.
• During the interphase that precedes meiosis I, the chromosomes of the
diploid cell start to replicate. As a result of replication, each chromosome
consists of two sister (genetically identical) chromatids, which are
attached at their centromeres. This replication of chromosomes is similar
to the one that precedes mitosis in somatic cell division.

76. NUCLEAR DIVISION: MITOSIS Mitosis,
as noted earlier, is the distribution of two
sets of chromosomes into two separate
nuclei.
The process results in the exact
partitioning of genetic information. For
convenience, biologists divide the process
into four stages: prophase, metaphase,
anaphase, and telophase. However,
mitosis is a continuous process; one stage
merges seamlessly into the next.

78. Meiosis, reproductive cell division.

79. Comparison between
mitosis (left ) and meiosis
(right) in which the
starting cell has two pairs
of homologous
chromosomes.

80. GENERAL PRINCIPLES OF CELL
COMMUNICATION
All organisms, whether unicellular or multicellular, need to
respond to their ever-changing environment in order to
survive and flourish.
Such responses are governed by the ability of cells to
sense physical changes and chemical cues occurring
around them.
The process of sensing and responding to extrinsic signals
is often termed cellular communication, although scientists
also use terms such as ‘signal transduction’ or ‘signalling’.
Cells respond to a wide range of extrinsic signals that
include chemical messengers (e.g. hormones, growth
factors, neurotransmitters), electrical impulses, mechanical
forces, pH, heat and light.

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