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If starfish
can grow a
new arm,
why can’t I?
STEM CELL

•
•

INTRODUCTION
MAINTENANCE
OF STEM CELL

SUE ®
WHERE DO I COME FROM?
GAMETES
FERTILISATION
ZYGOTE
 WHEN

GAMETE FUSED
MORULA
BLASTOCYSTS
IMPLANTATION
EMBRYO
 IMPLANTED

ZYGOTE TO 8TH WEEK
FETUS
HOW DOES A ONE CELL
ZYGOTE BECOME A
HUMAN?
Human

body composed of 50-75 TRILLION cells.
MORE THAN 220 TYPES OF CELL
DIFFERENTIATION
 GROWTH

FACTORS
 INTRACELLULAR SIGNALLING
 GENETIC MATERIAL

- TO BE CONTINUED IN NEXT PART
STEM CELL
 Ascending

stalk of a tree
 Also means 'to stop or to slow
down’
In this case, stop and slow down and turn
into other types of cells.
DIFFERENCE OF STEM CELL
AND NORMAL BODY CELLS
 Ability

to divide throughout life
(theoretically)
 Ability to differentiate into many different
cell types
TYPES OF STEM CELL
 EMBRYONIC

STEM CELL
 FETAL STEM CELL
 BERASHI CELL
 ADULT STEM CELL
POTENTIAL OF STEM CELL
Totipotent



stem cells

early embryos
Each cell can form a complete organism

Pluripotent



undifferentiated inner cell mass of blastocyst
form any of over 200 different cell types

 Multipotent


stem cells
stem cells

ability to differentiate is more limited
TOTIPOTENT STEM CELLS
 Up

to 8-cell stage of zygote
 No research work on totipotent stem cells
 Our aim is NOT to create a clone human
EMBRYONIC STEM CELLS
 Derived

from inner cell mass of blastocysts
 Pluripotent
1. Ectoderm
2. Mesoderm
3. Endoderm
 Able to replicate indefinitely
BLASTOCYSTS
ISOLATION OF EMBRYONIC
STEM CELLS
 SOURCE
•

SURPLUS EMBRYO – I.V. FERTILISATION

 TECHNIQUE
•
•

OF ISOLATION

MICROSURGERY
LASER-ASSISTED BLASTOCYST DISSECTION
MAINTENANCE OF EMBRYONIC
STEM CELLS
 STEM
-

CELL NICHE

in vivo or in vitro stem cell microenvironment

 Human

ES cells are often grown in

- fibroblastic growth factor-2 containing, fetal bovine
serum supplemented media
 Grown

on a feeder layer of cells

- supportive in maintaining the pluripotent
characteristics of embryonic stem cells
GERM LINE STEM CELLS
NICHE
HEMATOPOETIC STEM CELLS
NICHE
AGING OF STEM CELLS
 Occurs

when cultured in vitro
 Morphology is changed and their
proliferative capacity is decreased
 Causes:
1.
2.

reduction in niche signaling pathway
activity
accumulation of Reactive Oxygen species
(ROS)
BERASHI STEM CELLS
 Found

in cord and extra embryonic tissues
and membranes
 Formed only by TOTIPOTENT CELLS
 Umbilical cord banking
FETAL STEM CELLS
 Taken

from aborted fetal tissue
 Have the potential to be a greater kind
of cells that adult cells
ADULT STEM CELLS









Hematopoietic stem cells
Intestinal stem cells
Mesenchymal stem cells
Endothelial stem cells
Neural stem cells
Olfactory adult stem cells
Testicular cells
Mammary stem cells
HISTORY OF STEM CELL RESEARCH
REGENERATIVE MEDICINE
process of replacing or regenerating human
cells, tissues or organs to restore or establish
normal function
 grow tissues and organs in the laboratory and
safely implant them when the body cannot
heal itself




Advantages:
1.
2.

solve the problem of the shortage of organs
available for donation
solve the problem of organ transplant rejection
DEDIFFERENTIATION
CHALLENGES OF STEM CELL
RESEARCH
 If

the embryo = inanimate matter
-then the resistance to embryonic
stem cell research is ludicrous.
 If the embryo is alive, then embryonic
stem cell research is immoral.
one must differentiate between human
beings and persons.
Stem cells Introduction

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Stem cells Introduction

  • 1. If starfish can grow a new arm, why can’t I?
  • 3. WHERE DO I COME FROM?
  • 7.
  • 9.
  • 13. FETUS
  • 14. HOW DOES A ONE CELL ZYGOTE BECOME A HUMAN? Human body composed of 50-75 TRILLION cells. MORE THAN 220 TYPES OF CELL
  • 15. DIFFERENTIATION  GROWTH FACTORS  INTRACELLULAR SIGNALLING  GENETIC MATERIAL - TO BE CONTINUED IN NEXT PART
  • 16.
  • 17. STEM CELL  Ascending stalk of a tree  Also means 'to stop or to slow down’ In this case, stop and slow down and turn into other types of cells.
  • 18.
  • 19. DIFFERENCE OF STEM CELL AND NORMAL BODY CELLS  Ability to divide throughout life (theoretically)  Ability to differentiate into many different cell types
  • 20. TYPES OF STEM CELL  EMBRYONIC STEM CELL  FETAL STEM CELL  BERASHI CELL  ADULT STEM CELL
  • 21. POTENTIAL OF STEM CELL Totipotent   stem cells early embryos Each cell can form a complete organism Pluripotent   undifferentiated inner cell mass of blastocyst form any of over 200 different cell types  Multipotent  stem cells stem cells ability to differentiate is more limited
  • 22.
  • 23. TOTIPOTENT STEM CELLS  Up to 8-cell stage of zygote  No research work on totipotent stem cells  Our aim is NOT to create a clone human
  • 24.
  • 25. EMBRYONIC STEM CELLS  Derived from inner cell mass of blastocysts  Pluripotent 1. Ectoderm 2. Mesoderm 3. Endoderm  Able to replicate indefinitely
  • 27.
  • 28. ISOLATION OF EMBRYONIC STEM CELLS  SOURCE • SURPLUS EMBRYO – I.V. FERTILISATION  TECHNIQUE • • OF ISOLATION MICROSURGERY LASER-ASSISTED BLASTOCYST DISSECTION
  • 29.
  • 30.
  • 31.
  • 32. MAINTENANCE OF EMBRYONIC STEM CELLS  STEM - CELL NICHE in vivo or in vitro stem cell microenvironment  Human ES cells are often grown in - fibroblastic growth factor-2 containing, fetal bovine serum supplemented media  Grown on a feeder layer of cells - supportive in maintaining the pluripotent characteristics of embryonic stem cells
  • 33.
  • 34. GERM LINE STEM CELLS NICHE
  • 36. AGING OF STEM CELLS  Occurs when cultured in vitro  Morphology is changed and their proliferative capacity is decreased  Causes: 1. 2. reduction in niche signaling pathway activity accumulation of Reactive Oxygen species (ROS)
  • 37.
  • 38. BERASHI STEM CELLS  Found in cord and extra embryonic tissues and membranes  Formed only by TOTIPOTENT CELLS  Umbilical cord banking
  • 39.
  • 40. FETAL STEM CELLS  Taken from aborted fetal tissue  Have the potential to be a greater kind of cells that adult cells
  • 41. ADULT STEM CELLS         Hematopoietic stem cells Intestinal stem cells Mesenchymal stem cells Endothelial stem cells Neural stem cells Olfactory adult stem cells Testicular cells Mammary stem cells
  • 42.
  • 43.
  • 44. HISTORY OF STEM CELL RESEARCH
  • 45.
  • 46. REGENERATIVE MEDICINE process of replacing or regenerating human cells, tissues or organs to restore or establish normal function  grow tissues and organs in the laboratory and safely implant them when the body cannot heal itself   Advantages: 1. 2. solve the problem of the shortage of organs available for donation solve the problem of organ transplant rejection
  • 47.
  • 49. CHALLENGES OF STEM CELL RESEARCH  If the embryo = inanimate matter -then the resistance to embryonic stem cell research is ludicrous.  If the embryo is alive, then embryonic stem cell research is immoral. one must differentiate between human beings and persons.

Editor's Notes

  1. Hematopoietic stem cells Main article: Hematopoietic stem cell Hematopoietic stem cells are found in the bone marrow and give rise to all the blood cell types. Cord blood[9] is also a common example of adult stem cell that is considered multipotent. [edit] Hematopoietic stem cells Mammary stem cells provide the source of cells for growth of the mammary gland during puberty and gestation and play an important role in carcinogenesis of the breast.[10] Mammary stem cells have been isolated from human and mouse tissue as well as from cell lines derived from the mammary gland. Single such cells can give rise to both the luminal and myoepithelial cell types of the gland, and have been shown to have the ability to regenerate the entire organ in mice.[10] [edit] Intestinal stem cells Intestinal stem cells divide continuously throughout life and use a complex genetic program to produce the cells lining the surface of the small and large intestines.[11] Intestinal stem cells reside near the base of the stem cell niche, called the crypts of Lieberkuhn. Intestinal stem cells are probably the source of most cancers of the small intestine and colon.[12] [edit] Mesenchymal stem cells Main article: Mesenchymal stem cell Mesenchymal stem cells (MSCs) are of stromal origin and may differentiate into a variety of tissues. MSCs have been isolated from placenta, adipose tissue, lung, bone marrow and blood, Wharton's jelly from the umbilical cord,[13] and teeth (perivascular niche of dental pulp and periodontal ligament).[14] MSCs are attractive for clinical therapy due to their ability to differentiate, provide trophic support, and modulate innate immune response.[13] [edit] Endothelial stem cells Main article: Endothelial stem cell Endothelial Stem Cells are one of the three types of Multipotent stem cells found in the bone marrow. They are a rare and controversial group with the ability to differentiate into endothelial cells, the cells that line blood vessels. [edit] Neural stem cells Main article: neural stem cell The existence of stem cells in the adult brain has been postulated following the discovery that the process of neurogenesis, the birth of new neurons, continues into adulthood in rats.[15] The presence of stem cells in the mature primate brain was first reported in 1967.[16] It has since been shown that new neurons are generated in adult mice, songbirds and primates, including humans. Normally, adult neurogenesis is restricted to two areas of the brain – the subventricular zone, which lines the lateral ventricles, and the dentate gyrus of the hippocampal formation.[17] Although the generation of new neurons in the hippocampus is well established, the presence of true self-renewing stem cells there has been debated.[18] Under certain circumstances, such as following tissue damage in ischemia, neurogenesis can be induced in other brain regions, including the neocortex. Neural stem cells are commonly cultured in vitro as so called neurospheres – floating heterogeneous aggregates of cells, containing a large proportion of stem cells.[19] They can be propagated for extended periods of time and differentiated into both neuronal and glia cells, and therefore behave as stem cells. However, some recent studies suggest that this behaviour is induced by the culture conditions in progenitor cells, the progeny of stem cell division that normally undergo a strictly limited number of replication cycles in vivo.[20] Furthermore, neurosphere-derived cells do not behave as stem cells when transplanted back into the brain.[21] Neural stem cells share many properties with haematopoietic stem cells (HSCs). Remarkably, when injected into the blood, neurosphere-derived cells differentiate into various cell types of the immune system.[22] [edit] Olfactory adult stem cells Olfactory adult stem cells have been successfully harvested from the human olfactory mucosa cells, which are found in the lining of the nose and are involved in the sense of smell.[23] If they are given the right chemical environment these cells have the same ability as embryonic stem cells to develop into many different cell types. Olfactory stem cells hold the potential for therapeutic applications and, in contrast to neural stem cells, can be harvested with ease without harm to the patient. This means they can be easily obtained from all individuals, including older patients who might be most in need of stem cell therapies. [edit] Neural crest stem cells Hair follicles contain two types of stem cells, one of which appears to represent a remnant of the stem cells of the embryonic neural crest. Similar cells have been found in the gastrointestinal tract, sciatic nerve, cardiac outflow tract and spinal and sympathetic ganglia. These cells can generate neurons, Schwann cells, myofibroblast, chondrocytes and melanocytes.[24][25] [edit] Testicular cells Multipotent stem cells with a claimed equivalency to embryonic stem cells have been derived from spermatogonial progenitor cells found in the testicles of laboratory mice by scientists in Germany[26][27][28] and the United States,[29][30][31][32] and, a year later, researchers from Germany and the United Kingdom confirmed the same capability using cells from the testicles of humans.[33] The extracted stem cells are known as human adult germline stem cells (GSCs)[34] Multipotent stem cells have also been derived from germ cells found in human testicles.[35]