Lecture 20 - Angiogenesis Flashcards

1
Q

Diagram of Growth Factors & Receptors essential in 1) Vasculogenesis 2) Angiogenesis & 3) Lymphangiogenesis

A

On summary sheet

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2
Q

What are VEGF critical for? Can you survive without them?

A

Growth & proliferation of angioblasts (endothelial progenitors). Without them the embryo does not survive. (no vasculogenesis or lymphangiogenesis)

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3
Q

What is angiogenesis?

A

The formation of new BVs from pre-existing ones.

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4
Q

What is angiopoietin? Is it critical?

A

The blood vessel making protein. Yes, without it you die however later than you would if you didn’t have VEGF.

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5
Q

Why does Angiogenic Sprouting occur? How does it occur?

A

Once you have formed a closed system you need to start telling some of the BVs to grow out in a different direction. Uses attractant and repellant molecules (GFs) to do this (e.g. VEGF)

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6
Q

Does Angiogenic Sprouting occur in adults? When are the 3 times?

A
  1. Wound healing
  2. Formation of the placenta
  3. Cancer development
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7
Q

How do you get the angioblasts to form 2 very different products - e.g. arteries and veins.

A

Have a homogeneous population (angioblasts sitting close to each other). Switch on two different surface molecules & immediately get two very different products (arteries or veins).

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8
Q

How to the arteries and veins get their different supporting structures? What is one important supporting structure arteries must have? What growth factor does the artery use to get it?

A

Formation of the different phenotypes (e.g. arteries & veins) then brings with it formation of the different supporting structures.
Arteries develop a lot of vascular smooth muscle cells (vSMC). Veins don’t have this as they are not under the same amount of pressure.
Arteries use the growth factor platelet-derived growth factor-beta (PDGFB) to recruit the vSMC. Without this GF the BVs of the embryo leaks because they are v weak - haemorrhaging & aneurysms

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9
Q

What molecule regulates BBB endothelial development? Is it only found on the brain? Is it highly or lowly expressed?

A

GPR124 - a glucose transporter. V important! Die without it. Only expressed in the brain & v highly expressed. It is expressed during BBB development but also during cancer.

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10
Q

How does the lymphatic fluid move around the body?

A

Doesn’t rely on heart to pump it around. Has valves & body movement pushes it around.

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11
Q

Which transcription factor regulates the generation of the lymphatic vessels in the developing embryo? What happens if an embryo doesn’t have this?

A

Prox1 - without it fluid builds up & it dies

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12
Q

What are the two origins in which the vSMCs/pericytes can potentially be derived from?

A
  1. Mesoderm

2. Neural crest

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13
Q

Are large tumours highly or lowly vascularised?

A

Highly. Avascular tumours can’t expand.

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14
Q

What is the “angiogenic switch”

A

Separates the mutated oncogenes from forming either 1. a harmless tumour or 2. a lethal tumour. What separates the 2 is lethal tumours undergo angiogenesis.

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15
Q

We can stop tumours growing by targeting the GFs they use to undergo angiogenesis & form new BVs. Why doesn’t this treatment affect any of the other BVs in the body?

A

The other BVs in the body are no longer undergoing change and therefore are not affected.

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16
Q

Do tumours have lymph vessels? Can we target this as part of cancer treatment?

A

Yes they do. Yes we can - targeting VEGF-C stops the tumour developing lymph vessels & they explode