stim kells Flashcards

1
Q

What are stem cells

A

undifferentiated cells, capable of long term self renewal (through cell division) and can divide without limit

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2
Q

What happens to potency as stem cells differentiate

A

progressive restriction of developmental potential/loss of potency

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3
Q

Describe the different stem cells

A

totipotent, pluripotent, multipotent, unipotent

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4
Q

What do stem cells form when they divide

A

1) produces transient amplifying cell and also another stem cell
2) Or two populations of stem cells, one population reproduces itself as stem cells, other

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5
Q

True of false, more division occurs through TAC not stem cells

A

True

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6
Q

Why are adult stem cells important

A
  • Important to maintain cell populations that last for long periods of time and must be renewed
  • They generate the cell types of the tissue in which they reside
  • Important for continued production of cells in: epithelium, blood, muscle, liver and brain
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7
Q

Describe totipotent stem cells

A

cells from early mammalian embryo. Can form entire blastocyst (embryonic tissue and fetal placenta around it)

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8
Q

Pluripotent stem cells…

A

: can form embryo but not surrounding placental tissue. Give rise to 3 germ layers (ectoderm, endoderm, mesoderm)

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9
Q

Multipotent stem cells ..

A

can give rise to many cell types

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10
Q

Unipotent stem cells/commited stem cell…

A

Give rise to one cell type

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11
Q

Describe journey of embryonic stem cell

A
  • In the 3-5 day embryo (blastocyst)
  • Inner stem cell give rise to entire body
  • ESC include pluripotent and totipotent stem cells
  • Totipotent from blastocyst cells at 2 or 4 cell stage. I.e. can obtain complete blastocyst from cells at this stage (i.e. embryo+fetal placenta aka trophoblast)
  • Pluripotent – at 8 cell stage (but cells can’t generate complete blastocyst)
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12
Q

What are iPS cells

A

arise from adult specialised cells that have been reprogrammed genetixally to be like stem cells
• Using genetically manipulation (viral transfection/ using viral vectors) expression of 4 genes is sufficient to convert adult skin fibroblast into iPSCs.

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13
Q

How can iPS cells be used

A

• They can differentiate into desired cell types for in vitro models of disease (espeiclaly inaccessible cells like neurones) and could be used in stem cell transplantation therapy of “self” cells

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14
Q

Describe journey of stem cells in epithelium of gut

A

Stem cells at the base of layer and renew epithelium. Stem cells migrate upwards and as they do they differentiate towards the lumen
Basal cell layer contain few stem cells, mainly Transient amplifying cells. These have reduced diff capacity and make many terminally differentiated cells.

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15
Q

Why is base of epithelium dark when stained

A

dense staining as lots of nuclei present as lots of cells undergoing lots of cell division (stem cells).

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16
Q

How do diff cells take on specific identities

A

• Selective gene expression: terminally differentiated cells express types express specific proteins (e.g. Hb in erythrocytes)

17
Q

How is diff sequential process

A

developmental potential of cells become progressively restricted as they become more specialised. Cells start to differentiate before they exit cell cycle during G1 and enter G0 and thus terminal differentiation. Most cell types stay terminally differentiated (can’t re-enter cell cycle + differentiate again),

18
Q

Why are hepatocytes unique

A

can dedifferentiate and re-enter cell cycle to make new hepatocytes to rebuild liver

19
Q

Is genome affected by differentiation

A

• Genome of differentiated cells not normally altered in sequence

20
Q

What factors maintain and produce diff state

A

• Transcription factors and chromatin modification specify and maintain differentiated state

21
Q

How can TF and chromatin modification affect how cells diff

A

. TF that drive differentiation block cell cycle, methylation of promoters of inactive genes and deacetylation of associated histones means resulting chromatin is stably inactivated (heterochromatic) whereas active genes are stably activated by opposite mechanisms (chromatin is euchromatic). This stabilises differentiated state of cell,(by stabilising genes in inactivated/off state)

22
Q

Apart from TF and chromatin modification, how can differential gene expression be regulated

A
  • alternate splicing,
  • RNA editing
  • genomic rearrangements.
23
Q

How can alternate splicing lead to differential gene expression

A

specific gene has the ability to splice RNA with varying exons to make different proteins. Make cells different, using same gene but slicing RNA

24
Q

True of false: Pluripotent cells have specialised gene expression programmes but can still proliferate to different cell types

A

True

25
Q

How can cells be reprogrammed to become mesoderm

A

 Take ectoderm layer and transplant onto endoderm, Cells reprogrammed to become mesoderm by being in contact with underlying endoderm

26
Q

Describe how cells have plastic state

A

cells don’t know what they will become and change differentiation pathway based on contact with other cells.

27
Q

What is meant by juxtracrine signalling

A

Contact dependent signalling

28
Q

How is cell type specific transcription achieved -

A

Diffusible ligand binds to cell surface receptor/intracellular receptor (paracrine)

  • Cell surface ligand and receptor of adjacent cells interact – juxtracrine (contact dependent signalling)
  • Gap junctions – juxtracrine