Module 7: Developmental Biology Flashcards

1
Q

List the 4 different types of stem cells

A
  1. Totipotent
  2. Embryonic stem cells
  3. Adult stem cells
  4. Blastocyst
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2
Q

Discuss in detail: Totipotent stem cells

A
  • lasts for about 2 weeks

- can differentiate into all body cells and extra-embryonic cells (umbilical cord, placenta)

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3
Q

Discuss in detail: Embryonic stem cells

A
  • pluripotent ‘immortal’ cell that propagates indefinitely

- it is a cell that has the potential to differentiate into a cell of any germ layer

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4
Q

Discuss in detail: Adult stem cells

A
  • grown up, not necessarily belonging to adults
  • multi-potent, gives rise to limited cell types and do not divide indefinitely (age and lose regenerative potential)
    e.g. haematopoietic lineage (blood stem cells)
    ~blood stem cells
    ~platelets
    ~white blood cells
    ~erythrocytes
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5
Q

Discuss in detail: Blastocyst stem cells

A
  • inner cell mass
  • trophectoderm
  • pluripotent stem cells taken from inner cell mass
  • blastocysts last for 2 weeks before attached to mother
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6
Q

Discuss other definitions of types of stem cells

A
  • Autologous: stem cells from own body
  • Allogenic: stem cells from donor
  • Somatic stem cells: from body
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7
Q

Discuss how stem cell plasticity reduces over time

A
  • stem cells don’t revert back to undifferentiated states after being committed to a lineage (unless artificially induced)
  • e.g. lymphoid progenitor cells (immune system), myeloid progenitor cells (blood cells)
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8
Q

Discuss Blood therapies

A
  • bone marrow stem cell transplant

- repopulate bone marrow after chemotherapy

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9
Q

Discuss Vision therapies

A
  • cornea/epithelium can scar or retain water leading to loss of vision
  • limbic system stem cell deficiency can cloud vision and lead to blindness
  • new therapy, dispersed corneal cells cultured for 2 weeks on special substrates
    ~not as clear as the original limbic cells but ‘close enough’
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10
Q

Discuss skin therapies

A
  1. Human fibroblasts seeded
  2. Proliferate and full the scaffold
  3. Secret dermal collagen (etc. creating alive skin)
  4. Dermal matrix forms around scaffold
  5. Graft onto patient
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11
Q

List 7 overall points with regards to Generating pluripotent stem cells; the future of cloning

A
  • Sources of pluripotent stem cells
  • Somatic cell nuclear transfer (Dolly)
  • World’s first primate cloned embryonic stem cells 2007
  • Human induced pluripotent stem cells have been cloned
  • there are some problems with induced pluripotent stem cells
  • Transdifferentiation: the reprogramming of one cell type to another
  • Human neural stem cells to induce functional myelination
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12
Q

Discuss in detail: Sources of pluripotent stem cells

A
  • from IVF cells
  • from blastocysts with or without cloning
  • from foetus (foetal tissues, umbilical cord: only blood lineages)
  • from adult tissue induced pluripotent stem cells
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13
Q

Discuss in detail: Somatic cell nuclear transfer (Dolly)

A
  • Dolly the sheep was successfully cloned from a mammary somatic cell and a donor egg in 1996
    ~the nucleus is removed from an egg cell and replaced by a nucleus from a differentiated somatic (body) cell
  • the named her Dolly after Dolly Parton’s mammaries
  • success rates are low in SCNT
  • permission to clone using human embryos (autologous stem cells) limited in many countries (ethics)
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14
Q

Discuss in detail: The worlds first primate cloned embryonic stem cells (2007)

A
  • humans cloned in 2013

- no need for eggs

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15
Q

Discuss in detail: problems with induced pluripotent stem cells

A
  • low success
  • choice of somatic cell may have pre-existing mutation (if mutations are trying to be cured)
  • do transgenes cause mutations ?
  • does reprogramming cause mutations?
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16
Q

Discuss in detail: Transdifferentiation: the reprogramming of one cell type to another

A
  • made possible as all cell contain entire genome

- phenotype expressed is different for different types of cells

17
Q

Discuss in detail: Human neural stem cells to induce functional myelination

A
  • possibility of curing hypomyelination such as multiple sclerosis and Palizaeus-Merzbacher disease
  • engraftment of oligodendrocyte to produce myelin