Vascular Endothelium Flashcards

1
Q

Atherosclerosis is a …………. ……………………… ……………. of the arteries

A

Atherosclerosis is a chronic inflammatory disease of the arteries

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2
Q

Pathogenesis of Atherosclerosis: Response-to-injury Model

A
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3
Q

What are the three layers of blood vessels and what do they contain?

A

Blood vessels consist of THREE LAYERS (except for capillaries and venules)

Tunica Intima - ENDOTHELIUM

Tunica Media - Smooth Muscle Cells

Tunica Adventitia - Vasa Vasorum, Nerves

NOTE: The vasa vasorum is a network of small blood vessels that supply the walls of large blood vessels

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4
Q
A
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5
Q

What is contact inhibition?

A

Vascular Endothelium

There are subtle differences in different endothelia

Endothelia forms a single layer of cells in the blood vessel

When the endothelial cells divide they know that they have to form a monolayer and this is called CONTACT INHIBITION

Once formed, the endothelial cells are pretty stable, you don’t get a lot of new endothelial cells forming

You get formation of new endothelial cells if you need new blood vessels to form e.g. during healing

Endothelial cells regulate essential functions of blood vessels

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6
Q

The critical functions of endothelial cells involve affecting:

List 4

A

The critical functions of endothelial cells involve affecting:

Inflammation

Vascular Tone and Permeability

Angiogenesis

Thrombosis and Haemostasis

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7
Q

What is Contact Inhibition?

A

When the endothelial cells divide they know that they have to form a monolayer and this is called CONTACT INHIBITION

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8
Q

Regulation of Endothelial Homeostasis ​

What type of state do endothelial cells tend to maintain- healthy?

What type of state is there when you cut yourself?

How does atherosclerosis fit into this?

A

Regulation of Endothelial Homeostasis ​

In healthy tissue, the endothelial cells tend to maintain an anti-inflammatory, anti-thrombotic state

If you have some inflammation or you cut yourself, the endothelium flip to produce pro-inflammatory, pro-thrombotic, pro-angiogenic factors

The problem with atherosclerosis is that the endothelium receives a chronic number of stimuli due to the high pressure, high glucose etc. which translates to cellular signals which keeps the endothelia in an activated state thus stopping it from flipping back to the normal state

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9
Q

List some pathophysiological stimuli of endothelial dysfunction in Atherogenesis

A
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10
Q

Leukocyte recruitment in atherosclerosis

  • Recruitment of blood leukocytes into tissues takes place normally during inflammation: leukocyte adhere to the endothelium of ……….. ………………. …………. and transmigrate into tissues
  • In atherosclerosis, leukocytes adhere to activated endothelium of ……….. ………………. and get stuck in the subendothelial space
  • Newly formed ……….. ………………. ……… at the base of developing lesions provide a further portal for leukocyte entry
A

Leukocyte recruitment in atherosclerosis

  • Recruitment of blood leukocytes into tissues takes place normally during inflammation: leukocyte adhere to the endothelium of post-capillary venules and transmigrate into tissues
  • In atherosclerosis, leukocytes adhere to activated endothelium of large arteries and get stuck in the subendothelial space
  • Newly formed post-capillary venules at the base of developing lesions provide a further portal for leukocyte entry
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11
Q

Explain the process of luekocyte recruitment?

A

There are molecules on the leukocyte that allow them to interact with the endothelium but they are generally switched off

Some are not switched off (e.g. selectins) but these don’t have partners on the endothelium to bind to - so they might touch the endothelium then come away

When inflammation occurs, the endothelium gets activated and it starts to express ligands for the leukocytes

You have selectins on the leukocyte which can weakly interact with the endothelium and make the leukocyte roll

Inside the leukocyte there are signals which activate the integrins (switching them to the high affinity state)

The integrins can then strongly bind to the ligands on the endothelium

The leukocyte then binds, adheres and transmigrates

MO=inflammation factor

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12
Q
A
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13
Q

Endothelial Junctions

Leukocytes transmigrate by squeezing through endothelial junctions

Top Photo - green is the nuclei and red is a protein called V-cadherin which is present at the junctions

At the junctions, two endothelial cells are very close to each other and the cell membrane proteins on each cell bind in a ………………… way

This binding of membrane proteins creates a ……………..

The junctions can …………….. and …………….. to allow things to go through without the whole endothelium falling apart

NOTE: there are some mutations in some of the molecules involved in this process that are not compatible with life - there are babies born with mutations in leukocyte integrins who only live for around 3 months because they are unable to deal with infection

A

Endothelial Junctions

Leukocytes transmigrate by squeezing through endothelial junctions

Top Photo - green is the nuclei and red is a protein called V-cadherin which is present at the junctions

At the junctions, two endothelial cells are very close to each other and the cell membrane proteins on each cell bind in a homophilic way

This binding of membrane proteins creates a zipper

The junctions can zip and unzip to allow things to go through without the whole endothelium falling apart

NOTE: there are some mutations in some of the molecules involved in this process that are not compatible with life - there are babies born with mutations in leukocyte integrins who only live for around 3 months because they are unable to deal with infection

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14
Q

Venules vs Arteries

This is a problem in atherosclerosis because physiologically, this transmigration process occurs in the ………….. ………….. where the ………….. goes through the ………….. ………….. , meets the basement membrane and chews the basement membrane with enzymes allowing it to pass through to the tissue

If a leukocyte adheres to the inside of a coronary artery or aorta - once it has gone through the endothelium it’s going to find a big thick layer which it CAN NOT go through and this is how atherosclerosis starts

A

Venules vs Arteries

This is a problem in atherosclerosis because physiologically, this transmigration process occurs in the post-capillary venules where the leukocyte goes through the endothelial junctions, meets the basement membrane and chews the basement membrane with enzymes allowing it to pass through to the tissue

If a leukocyte adheres to the inside of a coronary artery or aorta - once it has gone through the endothelium it’s going to find a big thick layer which it CAN NOT go through and this is how atherosclerosis starts

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15
Q

Vascular Permeability

Increased permeability results in the leakage of plasma proteins through endothelial junctions into the subendothelial space

Right below the endothelium there is a layer of sticky molecules (collagen and proteoglycan)

A
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16
Q

Lipoprotein Trapping and Oxidative Modification

Here you have lipids and the yellow crosses are the sticky proteins in the subendothelium (collagen and proteoglycans)

When the endothelium becomes activated, the cholesterol goes under the endothelial layer

The LDLs then get modified as it is a very oxidative environment

The LDLs then get stuck in the subendothelial layer

The macrophages then come and phagocytose the LDLs forming FOAM CELLS

This is the source of the chronic inflammation

A
17
Q

Blood Flow

Atherosclerosis is not evenly distributed across the vasculature, it tends to occur at …………….. …………..

This is because you get …………….. ………….. at …………….. …………..

Name 3 things laminar blood flow promotes?

Name 4 things Turbulent flow promotes?

A

Blood Flow

Atherosclerosis is not evenly distributed across the vasculature, it tends to occur at BRANCH POINTS

This is because you get turbulent flow at branch points

Laminar flow can be sensed by the endothelium as a positive protective signal - this means that it triggers the production of a lot of protective molecules e.g. nitric oxide

Turbulent flow triggers the balance to go the other way and activates the inflammatory and thrombotic pathways

Laminar blood flow promotes:

Nitric oxide production

Factors that inhibit coagulation, leukocyte adhesion, smooth muscle cell proliferation

Endothelial survival

Turbulent blood flow promotes:

Coagulation, leukocyte adhesion, smooth muscle cell proliferation

Endothelial apoptosis

18
Q

Name 6 protective effects of nitric oxide (not nitrous)

A
19
Q

Endothlium exposed to laminar flow produces athero protective molecules- laminar flow activates athero protective pathways. Some of them are controlled by these transcription factors called KLF2 and KLF4.

The opposite occurs for turbulent flow and there is an upregulation of NF kappa B

A
20
Q
A
21
Q

What is angiogenesis?

When tissue is ………….., it will release chemicals which activates the existing blood vessels which triggers a change in the cells

The cells that becomes a tip cell takes over and controls the formation of the blood vessel

You end up with a stabilised blood vessel forming

A

When tissue is hypoxic, it will release chemicals which activates the existing blood vessels which triggers a change in the cells

The cells that becomes a tip cell takes over and controls the formation of the blood vessel

You end up with a stabilised blood vessel forming

22
Q

Angiogenesis plays a detrimental and beneficial role in cardiovascular disease

Angiogenesis plays a detrimental and beneficial role in cardiovascular disease

On one hand, angiogenesis promotes the………………… …… ……………….. ……………………

When you have an advanced plaque and it gets to a size where there is a lot of ……………….. debris inside and there is ……………….. - the ……………….. stimulates angiogenesis from the little vessels (……………….. ………………..)

The vasa vasorum vessels are ……………. and more leukocytes will come in and contribute to the growth of the atherosclerotic plaque

What is the beneficial side of angiogenesis?

A

Angiogenesis and Cardiovascular Disease - The Janus Paradox

Angiogenesis plays a detrimental and beneficial role in cardiovascular disease

On one hand, angiogenesis promotes the growth of atherosclerotic plaques

When you have an advanced plaque and it gets to a size where there is a lot of necrotic debris inside and there is hypoxia - the hypoxia stimulates angiogenesis from the little vessels (vasa vasorum)

The vasa vasorum vessels are fragile and more leukocytes will come in and contribute to the growth of the atherosclerotic plaque

ON THE OTHER HAND - one of the main problems for people who suffer from acute myocardial infarction is that the tissue which suffered ischaemia will become fibrotic and hence the patient will develop heart failure

Some interventional cardiologists had the idea that if we could act really quickly after an acute myocardial infarction to reoxygenate the myocardium downstream of the occlusion in the coronary arteries using THERAPEUTIC ANGIOGENESIS, we could prevent the tissue damage and hence prevent heart failure

This is the good side of angiogenesis in cardiovascular disease

23
Q

Define Senescence?

What is the bad thing about senescence?

What can induce Endothelial senescence?

As senescent cells have a ……………………… and ………………………. phenotype, they can contribute to atherosclerotic plaque progression

A

Senescence

Senescence applies to a lot of cells in the body

Senescence is growth arrest that halts the proliferation of ageing and/or damaged cells

This is a clever way of making sure that damaged cells don’t take over and is considered to be a protective mechanism against cancer

The bad thing about senescence is that senescent cells can develop a PROINFLAMMATORY PHENOTYPE

This is stained for senescent cells - shows that senescent cells are found in atherosclerotic lesions

Endothelial senescence can be induced by cardiovascular risk factors such as oxidative stress

As senescent cells have a pro-inflammatory and pro-thrombotic phenotype, they can contribute to atherosclerotic plaque progression

24
Q

Overview of Atherosclerosis

At the beginning you have risk factors which activate the endothelium and promotes permeability, leukocyte adhesion and leukocyte migration

Leukocytes which enter the subendothelial layer begin to phagocytose LDLs and form foam cells producing fatty streaks

After a long time, this becomes a large complex plaque with angiogenesis and senescence possible playing a role

NOTE: Red wine contains RESVERATROL which has anti-inflammatory properties on the endothelium

Red wine has a hormetic action - it is beneficial at lower doses and has cytotoxic effects at higher doses

A
25
Q

QUESTION

Q1. Which of these processes promotes early development of atherosclerotic plaque?

Senescence

Endothelial Activation

Thrombosis

Permeability

Q2. Physiologically, leukocyte transmigration occurs:

In large arteries

In post-capillary venules

In the aorta

A

ANSWERS:

2 and 4

2