L2 6 Mar 2019 Flashcards

Stem Cells: Disease and Regeneration

1
Q

stem cell

A
  • self renewal
  • differentiate into many different cell types
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2
Q

stem cell status in adults

A

most are quiescent, there are active ones in the gut though

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3
Q

blastocyst

A

used to derive pluripotent stem cells –> from inner cell mass

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4
Q

purpose of dissecting inner cell mass out of blastocysts

A

can create stem cell lines, used for cloning

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5
Q

what is the significance of which germ layer a stem cell comes from?

A

usually cells from the same germ layer can be “converted” (in some way) into each other

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6
Q

major stem cell types

A
  • embryonic stem cells
  • embryonic germ cells
  • adult stem cells
  • umbilical cord and placenta stem cells
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7
Q

stem cell niches (in tissues and organs)

A

stem cells naturally exist in a microenvironment, which acts as maintenance and supports normal function

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8
Q

examples of stem cell niches

A
  • haematopoietic stem cells are surrounded by stromal stem cells
  • brain stem cells are in the subventricular zone –> close to ependymal cells and close to blood vessels
  • skin stem cells in hair follicle bulge, called “bulge stem cells”
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9
Q

microglia

A

macrophage like cells in the brain

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10
Q

stem cell activation in the brain

A
  1. microglial activation
  2. activates astrocytes
  3. activates neural stem cells
  4. activates neural stem cells, however this won’t lead to a complete recovery due to the fact that we have limited stem cells
  5. always leads to some scarring (glial scar)
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11
Q

SCNT

A
  • asexual reproduction by somatic cell nuclear transfer
  • no sperm
  • transfers nucleus from mature cell to donor egg
  • requires stimulus to begin dividing
  • *functionally different* from regular egg
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12
Q

stem cell therapies

A

“autologist transplants” taking patient’s own cells and putting them back into the patient after cloning or something

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13
Q

molecular reprogramming

A

goal: manipulate somatic cell’s potency (increase it)

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14
Q

factors that can reverse normal adult cell to iPS (induced pluripotent cells)

A

Oct 3/4, Sox2, c-Myc, Klf4

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15
Q

adult stem cell

A
  • typically in or near their tissue
  • capable of giving rise to functional cells in their tissue
  • typically found in tissues with regular turnover
  • decrease in both number and activity as you age
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16
Q

embryonic stem cells

A
  • from inner cell mass
  • capable of giving rise to all of the cell types in the body (incl. non-regenerative)
  • can be divided many times in culture to make many cells
17
Q

umbilical cord and placenta stem cells

A
  • isolated immediately after birth
  • more flexible (pluripotent)
  • limited research tho
  • easily isolated and banked
18
Q

stem cell activation in the liver

A

up to 90% of the liver is restored

  1. priming: Kupffer cells release cytokines (IL-6) which acto on hepatocytes so parenchymal cells will receive and respond to growth factor signals
  2. growth factor: HGF and TGF-α act on hepatocytes, which take several hours to progress from G0 to G1 to S phases in the cell cycle
  3. after hepatocyte replication, nonparenchymal cell replication: Kupffer cells, endothelial cells and stromal cells
  4. termination: hepatocytes return to quiescence
19
Q

Pros and cons of cell souce for stem cell therapies

A
  • ES: grows well and is pluripotent; non-self and directed differentation
  • iPSC-self: grow well, pluripotent and self; directed differentiation, labour intensice and inefficient
  • neonatal: good availability, can be self; poor growth, numbers and cell type
  • adult: limited plasticity, can be self; poor growth, poor numbers/accessibility