1. introduction and definitions Flashcards

1
Q

when was the first idea that organs could be regenerated?

A

In Greek mythology, Prometheus and liver regeneration

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2
Q

when was the first BM transplant?

A

1950s - irradiated dogs that received BM transplant could recover

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3
Q

what experiments did John Gurdon conduct in the 1960s?

A

Nuclear transfer experiments - somatic nucleus of tadpole gut cell transferred into oocyte and from this an entire frog was generated

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4
Q

what two things did John Gurdon’s experiments show?

A
  • they showed that it was possible to take a somatic differentiated nucleus and reprogram it to an embryonic like state
  • they showed that the genome in each cell has all the information to convert a cell into an entire organism
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5
Q

where are embryonic stem cells derived from?

A

the inner cell mass of blastocysts

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6
Q

what are embryonic carcinoma cells?

A

these are stem cells of teratocarcinomas

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7
Q

give an example of a stem cell based tissue and how long does it take for it to entirely regenerate?

A

the skin takes one month to entirely regenerate

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8
Q

define lineage

A

the genealogical pedigree of cells related through cell division. cells of the same lineage may be derived from a common progenitor.

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9
Q

what is lineage tracing?

A

labelling a population of similar cells and seeing what these cell types give rise to

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10
Q

define clones

A

clones are the progeny of a single cell.

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11
Q

what is clonal analysis?

A

labelling a cell and seeing what it gives rise to

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12
Q

define differentiated cell

A

this is a cell with a specific function that is usually post-mitotic.

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13
Q

why is differentiated usually a multi-step process?

A

because there is normally a large difference between stem cells and differentiated cells

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14
Q

what is lineage commitment?

A

the restricted ability to give rise to a specific set of differentiated cells

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15
Q

what is the potency of a cell?

A

how many lineages a cell can produce

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16
Q

what is a cell that can give rise two lineages called?

A

bi-potent

17
Q

what is self-renewal?

A

the ability to undergo numerous cycles of cells division while maintaining the undifferentiated state

18
Q

what occurs to self-renewal of SC in the ageing process?

A

it becomes less efficient

19
Q

what is special about embryonic stem cell self renewal that does not occur in tissue stem cells self renewal?

A

embryonic stem cell self-renewal, unlike tissue stem cell self-renewal, is perfect. this means that ESC can be cultured forever.

20
Q

what is flow cytometry?

A

fluorescence activated cell sorting

21
Q

define the flow cytometry process? (4 steps)

A
  1. dissociated tissue
  2. label cells with antibody to specific marker of interest
  3. put cells in flow cytometry machine
  4. laser pushes out cells with antibody associated
22
Q

once cells are sorted by flow cytometry, how are they identified?

A

RNA-seq if cells are dead

if you are careful and they are still alive then you can culture them

23
Q

what are transit amplifying cells?

A

uni-potent, usually highly proliferative cells

24
Q

what is a stem cell?

A

stem cells are multipotent, self-renewing entities that are able give rise to specialised cells

25
Q

what is quiescence?

A

when a stem cell is held in G0 and not dividing

26
Q

where are the only totipotent stem cells found?

A

the zygote

27
Q

what can totipotent stem cells give rise to?

A

the embryo and extra-embryonic tissue

28
Q

what potency are ESC?

A

pluripotent

29
Q

what is gastrulation?

A

a phase in embryonic development when the blastula reorganises into a trilaminar known as the gastrula

30
Q

what are the three germ layers?

A

ectoderm, mesoderm and endoderm

31
Q

what is set aside very early on in development?

A

primordial germ cells

32
Q

what is different about the potency of ESC and adult stem cells?

A

ESC are pluripotent

adult stem cells are multi/uni-potent

33
Q

are adult stem cells easy to culture like ESC?

A

no, they are very hard and potentially impossible to culture sometimes