Cell-substrate interactions 4 Flashcards

1
Q

What do current biomaterial research look to achieve

A

Producing a scaffold/substrates for the cells and tissue in the body to interact with along with guidance molecules and become the replacement tissue.
This has also been used in the lab to replace this damaged tissue.

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2
Q

Give an example of current biomaterials

A

Porous hydroxyapatite or colalgen.

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3
Q

What is one of the main drivers for biomaterials

A

Lack of organ transplants

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4
Q

What is a bioreactor

A

This allows a dynamic environment for these cells to grow in instead of the traditional static environment (e.g. 37C at 5% O2)

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5
Q

What are the benefits of bioreactors

A

Can produce more cells than static culture
Can limit static environments effects on cells
Simulates the body
Still cultured on a porous scaffold

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6
Q

What did Holtorf et al 2005 find regarding bioreactors effects on mesenchymal stem cells

A

Osteopontin was used as a marker for osteoblast differentiation
The use of a biomarker and a dynamic culture showed that osteopontin levels were significantly higher with or without dexomethasone in comparison to static conditions.

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7
Q

How else can cell behaviour be stimulated in tissue engineering and give some examples

A

Growth factors -

  • Transforming growth factor-beta (TGF-β)
  • Bone morphogenetic protein (BMPs)
  • Fibroblast growth factor (FGFs)
  • Insulin-like growth factor (IGFs)
  • Platelet-derived growth factor (PDGFs)
  • Vascular endothelial growth factor (VEGFs)
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8
Q

What can these growth factors do to these cells

A

Cell proliferation
Cell migration
Cell differentiation
Stimulate increased growth factors or signalling molecules

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9
Q

How are these growth factors added

A

In vitro -

Externally via medium
Stimulating cell synthesis of GFs
Using another cell type to release GF and the cell medium to respond

In vitro -
Via tethering to scaffold

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10
Q

What did Bane 2009 use GFs for bones

A

Recombinant human bone morphogenetic protein 2 (rhBMP-2) as a bulking agent for vertebral fractures with a plate
66% fusion in control
95% fusion in GF exposed

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11
Q

What is one risk of GF use

A

Cancer

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12
Q

What is the future of tissue engineering

A

3D bioprinting of tissues and organs, specific to each patient - to form suitable scaffolds.

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13
Q

What is one debated point regarding bio-scaffolds

A

Cells are initially influenced by the scaffold but they then modify them by secreting their own scaffold and degrading the ECM.

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14
Q

How was 3D ECM scaffold used for cystoplasty

WIDER READING - Atala 2006

A

Took 7 patients with end-stage bladder disease and took a bladder biopsy from them which after 7 weeks an engineered bladder was formed with autologous cells seeded on collagen-polyglycolic acid scaffolds and wrapped in omentum.

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15
Q

How was tissue-engineering used to make a trachea

WIDER READING -Macchiarini 2008

A

Cultured mesenchymal stem cell derived chondrocytes from host which was inmplanted into the patient allowing her to have a functional airway by 4 months
Patient had end-stage bronchomalacia.
Was on no immunosuppresion

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16
Q

How was tissue engineering used for vascular grafts

WIDER READING - Tiwari 2001

A

Carried out in vitro-growth of blood vessels from saphenous or carotid artery which have been grown in a lab and been used on damage vessels without causing an immune response.

17
Q

What are some of the issues with using growth factors in tissue engineering

WIDER READING - Ren et al 2020

A

Short half-life
Rapid diffusion from delivery site
Low cost-effectiveness

18
Q

What is one way to keep GFs present for longer

WIDER READING - Ren et al 2020

A

Covalently bond them to immobilize them. They are then activated when the biomaterial is degraded or cleaved

19
Q

How was 3D printing used for tissue engineering

WIDER READING - Kim 1998

A

Hepatic cells and nonparenchymal cells attached and survived on the 3D polymer scaffolds once implanted where previously inadequate oxygen diffusion as the culture grows is usually its demise once transplanted