Vascular Biology II Flashcards

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1
Q

What type of junctions are found in continuous capillaries?

A

Tight junctions between endothelial cells. One cells folds over the other cell “marginal folds”

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2
Q

Do endothelial cells have pores of fenestrae?

A

NO

endothelial cells lack pores or fenestrae

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3
Q

How is information transferred in endothelial cells within continuous capillaries?

A

numerous pinocytotic vessicles

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4
Q

Where are continuous capillaries located? (4)

A

1) Brain
2) Muscle
3) Connective Tissue
4) Exocrine Glands

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5
Q

Where are fenestrated capillaries located?

A

Where rapid exchange of substances between the blood and tissue occurs

1) Kidney, nonglomerular
2) Endocrine glands
3) Intestines
4) Kidney [glomerulus- diaphrafms absent]

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6
Q

Describe the fenestrae (pores) present in the endothelial walls of fenestrated capillaries?

A

Pores are usually closed by a thin diaphragm

the basal lamina is continuous

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7
Q

How does the diameter of fenestrated capillaries compare to continuous capillaries?

A

They have the same diameter (5-10 micrometers)

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8
Q

Which type of capillary has a large opening between the endothelial cells?

A

Sinusoidal

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9
Q

Describe the basal lamina of the three different types of capillaries.

A

Continuous: well-developed
Fenestrated: continuous
Sinusoidal: DISCONTINUOUS OR ABSENT

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10
Q

What capillary type is associated with macrophages?

A

sinusoidal

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11
Q

Which type of capillary has the largest diameter?

A

sinusoidal (30-40 micrometers)

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12
Q

Where are sinusoidal capillaries located?

A

In areas of rapid exchange and where cells can be exchanged

1) Red bone marrow
2) Liver
3) Spleen
4) Adrenal cortex

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13
Q

What are the smallest types of veins?

A

Pericytic and muscular venules

Pericytic are smaller of the two

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14
Q

Veins have valves which can be used to indicate blood flow direction.

A

Look at the picture and know this.

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15
Q

What is the key identifier of large veins?

A

Longitudinal bundles of smooth muscle in the adventitia

*longitudinal arrangement allows contraction that pushes the blood back to the heart

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16
Q

Define vasculogenesis.

A

De novo vessel formation

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17
Q

Define angiogenesis.

A

Growth from existing EC-derived channels.

18
Q

Define arteriogenesis.

A

Formation of arteries, arterioles, and collateral vessel remodeling

19
Q

Define neovascularization.

A

Overarching term to include vasculogenesis, angiogenesis, and arteriogenesis.

20
Q

Define remodeling.

A

Vascular response to alterations in the environment.

21
Q

What are the two mechanisms of blood vessel formation in the adult?

A

1) From endothelial percursor cells (EPCs)

2) From pre-existing vessels

22
Q

Which blood vessel formation method do tumors use?

A

BOTH

tumor angiogenesis employs both mechanism

23
Q

What are EPCs?

A

angioblast-like cells that reside in the red bone marrow of adults and non-bone marrow niches

24
Q

Describe EPC blood vessel formation. (What 3 things can they do?)

A

EPCs mobilize from niche and migrate to blood vessel formation site where they

1) Replace lost endothelial cells
2) Re-endothelize vascular implants
3) Neovascularize ischemic organs, wounds, or tumors

25
Q

List the 6 basic steps to blood vessel formation from pre-existing blood vessels.

A

1) Vasodilation (NO) and increased permeability (VEGF)
2) Degradation of BL mediated by MMPs and disruption of intracellular junctions mediated by plasminogen activator.
3) ANG-2 destabilizes vessels.
4) Migration and proliferation of endothelial cells mediated by VEGF and FGF.
5) Formation of endothelial capillary tube.
6) Elaboration of BL by TGF-B and recruitment of periendothelial cells (pericytes of SMCs) mediated by ANG-1-TIE-2 and PGDF.

26
Q

What is the difference between ANG 2 and ANG 1?

A

ANG-2 destabilizes

ANG-1-TIE-2 stabilizes

27
Q

What is the function of NO?

A

Vasodilation of pre-existing blood vessel

28
Q

What is the function of VEGF?

A

1) increased vascular permeability of pre-existing vessel

2) induces migration and proliferation of endothelial cells

29
Q

What is the purpose of MMPs?

A

Proteolytic degradation of the basal lamina of the parent vessel by metalloproteinases

30
Q

What mediates the loss of cell-to-cell contact?

A

Plasminogen activator

31
Q

What three factors mediate the endothelial cell migration and proliferation?

A

VEGF
angiopoietin 2
Fibroblasst growth factor 2

32
Q

What periendothelial cells are recruited in blood vessel formation?

A

1) Pericytes for capillaries

2) Pericytic venules and smooth muscle cells for larger vessels

33
Q

What factor is responsible for elaboration of basal lamina elements?

A

TGF-beta

transforming growth factor

34
Q

What mediates the recruitment of periendothelial cells?

A

Interaction of Ang 1 with the Tie2 receptor on endothelial cells

35
Q

What is the function of PDGR (platelet derived growth factor)?

A

Induces recruitment of smooth muscle cells

36
Q

How is Ang 2 involved in the remodeling process?

A

by blocking the stabilizing function of Ang 1

37
Q

What are 6 potential clinical benefits of proangiogenesis ?

A
MI (myocardial ischemia)
Peripheral ischemia
Cerebral ischemia
Wound healing and fracture repair
Reconstructive surgery
Transplantation of islets of Langerhans
38
Q

What are 6 potential clinical benefits of antiangiogenesis?

A
Tumor growth and metastases
Ocular neovascularization
Hemangiomas
Rheumatoid arthritis
Atherosclerotic plaque neovascularization
Birth control
39
Q

How can endothelial cells of tumor vessels be specifically targeted?

A

They express a prtn called tumor endothelial marker 8 (TEM8)

Since this prtn is preferentially expressed in tumor vessels, the marker ca be used to specifically deliver drug molecules to tumor vessels

40
Q

Why can the great saphenous vein be used in coronary bypass surgery?

A

Atypical vein: 2 or 3 layers of smooth muscle in its media

Wall remodeling will occur after the bypass to make it even more suitable!