2 Stem Cells & Tissue Engineering Flashcards

1
Q

What are the SIMILARITIES between determination & differentiation? (3)

A

1) both result not from changes in genes, but changes in gene EXPRESSION (except for immune system & gametes)
2) both result from alteration in chromatin structure and transcription factor expression
3) both are often quite permanent and heritable through many cell divisions

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2
Q

What are the DIFFERENCES between determination & differentiation?

A

1) Determination occurs prior to overt differentiation
2) Differentiation results in the cell’s acquisition of functional properties (via shape polarity, orientation w respect to neighbours, appropriate organelles & proteins which enable it to carry out metabolic signalling, transport or contractile functions required in a particular tissue, etc.)

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3
Q

Define cell plasticity.

A

Cells that are normally committed to one lineage can be switched to a different lineage pathway

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4
Q

What are the 3 processes in which cell plasticity may be observed? Define them.

A

1) TRANSDIFFERENTIATION: conversion of 1 mature cell type to another mature cell type
2) METAPLASIA: conversion of 1 tissue type to another tissue type
3) DE-DIFFERENTIATION: reversion of a mature cell to a stem or progenitor state
- optional- 4) REPROGRAMMING of a cell of any potency to pluripotency (iPS)

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5
Q

Under what conditions can plasticity be observed? (2)

A

1) Tissue damage and regeneration

2) Experimental induction via ectopic expression of master regulator transcription factors (iPS)

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6
Q

Give an example of metaplasia occurance.

A

BARRETT’S OESOPHAGUS
CAUSE: GI reflux (acid reflux from stomach) causes tissue damage
EFFECT: squamous epithelial lining of oesophagus is converted into something resembling intestinal lining

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7
Q

Define the capabilities of a TOTI-, PLURI-, and MULTIpotent cell.

A

TOTI: can give rise to a new individual given apropriate maternal support
* restricted to very early stages of development (max. morula/blastula)
PLURI: can give rise to all types of adult tissue cells + extraembryonic tissue (cells which support embryonic development)
MULTI: can give rise to several types of mature cells

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8
Q

What are the 3 types of adult tissues / adult stem cells / tissue stem cells? Give explanations and/or examples where possible.

A

1) CONTINUOUSLY renewing
e. g. bone marrow, skin
2) CONDITIONALLY renewing: turnover still occurs but at a much slower rate; unless tissue damage occurs, SCs or other mechanisms to replace damaged cells are quiescent.
e. g. liver, kidney
3) NON renewing: actually just extremely slow turnover
e. g. cardiac muscle

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9
Q

What is the definition of a stem cell? (2013 Q6a, 6m)

Hint: 2 key properties

A

A primitive cell which can either self-renew or give rise to more specialised cell types i.e. SCs are the ancestors at the top of family tress of related cell types.

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10
Q

What are the characteristics of stem cells? (8)

A

1) capable of self renewal and differentiation
2) responds to signals which regulate their growth & proliferation, enabling them to meet changing demands
3) may give rise to transit amplifying cell compartment(s)
4) are often lacking specialised organelles / show high nucles:cytoplasm ratio
5) contain long-lived expressed telomerases
6) are slowly dividing
7) few in number / form a minority component in tissues
8) may be restricted spatially to specific zones / niches e.g. gut’s crypt

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11
Q

What is a transit amplifying cell compartment?

A

An area containing cells which are not fully differentiation but still multiplying, essentially amplifying the number of cells heading towards a particular lineage.

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12
Q

What markers can be used to identify specific differentiation stages in cell linaeges? (4)

A

1) transcription factors
2) cell surface moleucles
3) cytostructural molecules e.g. intermediate filaments
4) specific functional gene products

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13
Q

The discovery of novel stem cell populations disproved the previously held notion that some tissues are static. List the findings on adult neurogensis as discussed in lectures. (3)

A

1) occurs in subventricular zone (SVZ) & hippocampus
2) new neurons from the SVZ wind up in olfactory epithelium
3) hippocampal neurogensis may have a role in learning & memory

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14
Q

What are the 4 types of differentiated gut cells and their function(s)?

A

1) ENTEROCYTES: absorb digested food i.e. macronutrients
2) GOBLET CELLS: produce mucin, which protects the intestinal lining from its contents
3) ENTEROENDOCRINE CELLS: produces gut hormones
4) PANETH CELLS: produces defensins & lysozome of the innate immunity

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15
Q

What is a stem cell niche? (2012 Q5b, 3m)

A

A very speicifc micro environment

  • containing cells producing extrinsic factors to
  • exert precise control over SC renewal & differentiation.
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16
Q

What are reserved stem cells?

A

Quiescent SCs that are

  • not dividing and
  • activated during damage
17
Q

Give an example of conditional renewal (organ + disease)

Hint: ‘cleaning’ organ

A

LIVER contains facultative SCs.
Regeneration occurs via
- proliferation of hepatocytes or
- bipotential stem cells found in biliary tree.
BILIARY ATRESIA:
CUASE: congenital blockage of extrahepatic bile duct -> cirrhosis
EFFECT: bipotential biliary cells proliferate in attempt to repair damage

18
Q

List the properties of pluripotent SCs. (3)

Hints: cloning, chimera

A

1) grows indefinitely in vitro
2) maintain normal genetic makeup
3) cloned lines maintain their donors’ developmental capacity and are capable it (differentiation) at high frequencies & under a range of conditions

19
Q

What is a teratoma?

A

a benign growth containing a number of different cell types foreign to the tumour’s location.

20
Q

What are the issues associated with somatic cell nuclear transfer with regards to patient specific therapy? (growing organs from affected individual’s ES cells to be used on same individual)

A

Difficult to implement; very inefficient

  • hundreds of eggs (rare resource) required to make 1 embryo
  • harvesting large numbers of oocytes carries risks
21
Q

Name the 2 types of pluripotent stem cells.

A

1) EMBRYONIC SCs (ES cells)

2) INDUCED PLURIPOTENT SCs (iPSC)