L11 - Vascularisation Flashcards

1
Q

In TE constructs what does vascularisation do?

A
  1. Avoids graft necrosis
  2. Generates thicker tissues
  3. Helps innervation
  4. Improves graft function
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2
Q

What is vasculogenesis?

A

De novo b.v. formation from progenitor cells

Mesoderm - hemangioblasts - tube formation - primary cap plexus

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3
Q

What is angiogenesis?

A

New blood vessel formation via extension/remodelling of existing blood vessels. Driven by hypoxia - release of VEGF - MMP breaks down BM - endo cells create vasc sprouts that move toward source of VEGF - recruitment of smooth muscle and pericytes
Can be physiological (period) or pathological (tumour angiogenesis)

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4
Q

What are the important factors involved in angiogenesis?

A

VEGF, hypoxia inducible factor, PDGF, angiopoietin, MMPs

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5
Q

What is arteriogenesis?

A

Maturation of blood vessels via increase in the fluid sheer stress e.g. due to occlusion. Endo cells release GFs - prolif of endo and smooth muscle cells

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6
Q

What are the approaches for vascularisation?

A

Scaffold design - porous scaffold

Scaffold functionalisation - GF delivery, controlled release is crucial

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7
Q

Explain the study - Polymeric system for GF delivery

A

VEGF - initiate angio but can’t promote maturation
PDGF - promotes maturation
HYPOTHESIS - dual delivery - formation of mature vasculature
2-stage relase:
1. VEGF mixed with scaffold polymer - stim growth
2. PDGF encap in microspheres to facilitate maturation
SLOW - may not be quick enough to prevent necrosis

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8
Q

Prevascularisation strategies

A

In vitro

  • TE cultured in vitro to build prevasc structures
  • Network can connect with exisiting bv in tissues
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9
Q

Prevascularisation strategies

A

In vivo

  • Implant in easy access, well vasc site - after connections have been made, TP to damaged site
  • Can be in muscle flap - take flap with TE construct
  • AV loop - spontaneous sprouting of vessels. No need to embed in muscle
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