MOD Week 1 Flashcards

1
Q

What is the function of cyclins and CDKs?

A

Control cell cycle

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2
Q

What cyclins and CDKs are used at what parts of the cell cycle?
Hint: Think full name

A

G1-S Cyclin E and CDK2
S-G2 Cyclin A and CDK2
G2-M Cyclin B and CDK1
M-G1 Cyclin D and CDK2

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3
Q

Which checkpoint is most commonly altered in cancer cells?

A

R just after G1

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4
Q

Why is R refered to as the point of no return?

A

Once the cells pass this point they will complete a full cell cycle

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5
Q

what mechanism allows apoptosis and DNA repair to take place at checkpoints?

A

p53

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6
Q

Describe how CDKs and cyclins control the cell cycle

A

Cyclin binds to substrate and activates CDK

CDK causes phosphorylation and chemical modification of that substrate whilst bound to Cyclin

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7
Q

How do we classify cells?

A

dependent on ability to multiply

Labile- stem cells divide persistently to replenish losses

stable- stem cells are usually quiescent, or proliferate very slowly. they can change to proliferate persistently when required (requires protoncogenes to change from G0 to G1)

permanent- stem cells are present but cannot do effective proliferation in response to significant cell loss

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8
Q

Name some labile cell populations

A

Surface epithelia, bone marrow

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9
Q

Name some stable cell populations

A

liver hepatocytes, bone osteoblasts

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10
Q

Name some permanent cell populations

A

brain neurones, cardiac and skeletal muscle

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11
Q

Name the 5 cellular adaptations undertaken by a cell

A
regeneration 
hypertrophy
hyperplasia
atrophy
metaplasia (changing from one cell type to another)
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12
Q

Name some tissues which can undergo regeneration

A

Liver

CNS can establish different pathways (plasticity)

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13
Q

are regenerated cells as good as the original cells?

A

usually, but not always and not immediately

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14
Q

how many times can a cell regenerate?

A

Depends on longlivity of a cell and the HAYFLICK constant. In humans this is 61.3

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15
Q

What is reconstitution. what are some examples?

A

Replacement of part of the body

Deer antlers, lizards tail

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16
Q

Define reconsistution and give some examples

A

Forming an area of cells again which are all different types.
If the end of a finger is removed before the age of 4 and a half years it will grow back completely

17
Q

Give some examples of hyperplasia

A

proliferation of endomedutrium under influence of oestrogen
bone marrow producing erythrocytes in reponse to hypoxia (altitude)
Can also cause pathological results e.g. goitre, eczema of the skin from excessive hyperplasia

18
Q

What cell type does hypertrophy most commonly occur in and why?

A

permanent cells because they cannot divide and so this is the only way they can respond to increased demand

It is caused by increased functional demand or hormonal stimulation

19
Q

Give examples of hypertrophy

A
body building of skeletal muscle
pregnant uterus (uses hyperplasia as well)
20
Q

Give an example of pathological hypertrophy

A

hypertension or valve problems

21
Q

In hypertension, the heart is enlarged and causes bad affects on a human. An athlete will also have an enlarged heart. Why is this not a problem

A

They are allowed time to rest after heavy exertion (e.g. after finishing a race). In hypertension, the heart is never able to rest.

22
Q

Why is childhood obesity such a problem?

A

Creates adipocytes, which once they are made will never leave and are capable of filling with fat later in life.

23
Q

How is atrophy different to hypertrophy?

A

Atrophy is shrinkage OR decrease in NUMBER of cells

Hypertrophy is increase in size (hyperplasia does numbers)

24
Q

what is lost in osteoporosis?

A

bone mass. NOT CALCIUM.

Note: can cause crush fractures of thoracic vertebrae due to loss of mass.

25
Q

Give examples of pathological atrophy?

A

atrophy of disuse e.g. muscle
denervation atrophy e.g. wasted hand after median nerve damage
inadequate blood supply e.g. peripheral vascular disease
loss of endocrine stimulation e.g. menopause and reproductive organs
senile atrophy from aging e.g. brain, heart
pressure on tissues around an enlarging benign tumour (normally secondary to ischaemia)

26
Q

What disease causes cerebral atrophy?

A

Alzheimer’s

27
Q

Why may cells undergo metaplasia?

A

Cells are stressed and change into cells which can cope more easily with this stress. The change is reversible.

28
Q

Give 2 examples of metaplasia

A

Smokers- pseudostratified ciliated brochial epithelium metaplases to stratified squamous epithelium due to effect of cigarette smoke causing stress

Barrett’s oesophagus- stratified squamous epithelium metaplases to gastric glandular epithelium with persistent acid reflux

29
Q

What danger is associated with metaplasia?

A

That the tissue becomes dysplastic and malignant

30
Q

Why is most commonly affected in metaplasia and why?

A

Epithelia as most susceptible to irritants as they cover other structures to form physical barrier.

31
Q

What is HYPOplasia?

A

NOT THE OPPOSITE OF HYPER

CONGENITAL CONDITION of underdevelopment of a tissue or organ at embryonic stage due to an inadequate number of cells. It is on a spectrum with aplasia (which is complete inability for an organ to develop or function normally).

32
Q

Describe aplasia

A

Complete failure of a specific tissue or organ to develop in embryonic development

e.g. Thymic aplasia resulting from infection and auto-immune problems, aplasia of the kidney

Can also be used to describe an organ whose cells have ceased to proliferate e.g. aplasia of bone marrow in aplastic anaemia

33
Q

Define atresia

A

Not forming an opening e.g. anus/vagina

34
Q

Define dysplasia

A

Proliferation of abnormal cells within a tissue which are precancerous, causing enlargement of that tissue.