4.Stem cells and apoptosis Flashcards

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1
Q

what are stem cells

A

Stem cells are non-specialised cells that can divide and differentiate into different specialised cells

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2
Q

what is meant by stem cell ‘potency’

A

the varying capacity into which stem cells are able to differentiate into

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3
Q

two main types of stem cells

A

-adult stem cells
-embryonic stem cells

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4
Q

identify the order of stem cell potency from most to least potent

A

-totipotent
-pluripotent
-multipotent

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5
Q

what is meant by totipotent

A

the capacity to differentiate into all possible cell types, including extra embryonic tissue

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6
Q

what is meant by pluripotent

A

the ability to differentiate into all cell types, except those that make up the placenta

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7
Q

what is meant by multipotent

A

the potential to give rise to cells from multiple, but a limited number of lineages

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8
Q

what is the potency of adult stem cells

A

multipotent

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9
Q

source of adult stem cell

A

adult stem cells are isolated from tissue samples

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10
Q

examples of adult stem cell for medical use

A

-bone marrow transplantation
-regenerative medicine

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11
Q

examples of adult stem cell use in research

A

-testing new drugs for safety and effectiveness
-model for studying how diseases develop

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12
Q

what is the potency of embryonic stem cells

A

pluripotent

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13
Q

source of embryonic stem cells

A
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14
Q

ethical issues raised by stem cells

A

-human embryos are destroyed when stem cells are extracted

-offering unproven stem cell therapies to those who are desperate

-

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14
Q

ethical issues raised by stem cells

A

-human embryos are destroyed when stem cells are extracted

-offering unproven stem cell therapies to those who are desperate

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15
Q

What is the term that is used to refer to an embryo that is 5 days old and consists of two groups of cells: Trophoblast and Inner cell mass?

A

blastocyst

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16
Q

define apoptosis

A

apoptosis is the natural and controlled death of cells in the body. It’s also known as programmed cell death

17
Q

what is the purpose of apoptosis

A

-allows old and/or damaged cells to be removed in your body
-allows infected cells to be removed in your body
-allows unnecessary/unwanted cells to be removed during embryonic development

18
Q

two pathways that can initiate apoptosis

A

-mitochondrial pathway (intrinsic)
-death receptor pathway (extrinsic)

19
Q

step 1 of apoptosis

A

a damaged cell or unwanted cell receive signals that initiate apoptosis

20
Q

step 2 of apoptosis

A

once signals are received by the cell, it leads to activation of capsazes

21
Q

what are capsaze enzymes

A

group of enzymes that can cleave intracellular proteins

22
Q

step 3 of apoptosis

A

as the digestion of cell contents continues, the cell starts to shrink and its membrane starts to bulge out, forming blebs

23
Q

step 4 of apoptosis

A

the cell will eventually be broken down into small chunks called apoptotic bodies

24
Q

apoptosis vs necrosis

A

-programmed and regulated cell death vs unexpected cell damage/death
-cell shrinks and contents are held in apoptotic bodies vs the cells contents swell and burst
-no inflammation vs inflammation

25
Q

too much apoptosis

A

can lead to degenerative diseases
-eg alzheimers

26
Q

briefly describe alzheimers disease

A

neurones begin to die leading to brain shrinkage. Because of increased apoptosis

27
Q

too little apoptosis

A

-reduced cell death
-can lead to tumours

28
Q

what is a tumour

A

a mass of abnormal cells
-in the sense that they divide uncontrollably and lack normal shape and structure
-cant undergo apoptosis naturally instead are flagged by the immune system

29
Q

G1 checkpoint

A

-inspects for DNA damage and cell size

30
Q

metaphase checkpoint

A

confirms that spindle fibres have correctly attached to the centromeres of replicated chromosomes

31
Q

G2 checkpoint

A

confirms that DNA has correctly replicated in the s phase

32
Q

important proteins involved in apoptosis

A

-capsaze enzymes
-death receptors

33
Q

what happens if DNA damage isn’t repaired

A

-may lead to mutations in genes that code for proteins
-mutated genes may code for less or non functional proteins
-hence a reduced rate of apoptosis
-mutated cells are able to go through the cell cycle with further mutations to their DNA leading to formation of tumours

34
Q

two classifications of tumours

A

-benign tumours
-malignant tumours (aka cancers)

35
Q

characteristics of benign tumours

A

-relatively slow growing masses of cells that tend to stay together within a capsule
-hence they can’t seperate and invade other parts of the body
-benign tumours can be removed by radiation therapy, often successful

36
Q

characteristics of malignant tumours

A

-benign tumours cells can mutate further and become malignant when they gain the ability to invade nearby tissue and/or enter the bloodstream or lymphatic system

37
Q

metastasis

A

malignant tumour cells can travel to other parts of body and grow into new malignant tumours

38
Q

why are cancers (malignant tumours) dangerous

A

-these tumours can grow in amongst healthy tissues and affect the structure of the healthy tissues
-if the structure of an organ is compromised by a tumour then then the function if the organ will be compromised too.

39
Q

what causes cancer

A

carcinogens-are any substance that can increase the likelihood of developing malignant tumours
eg uv light increases risk of skin cancer