L4 - bioengineered skin Flashcards

1
Q

why do we need to engineer skin

A

for clincal needs:
- burns
- plastic surgery
-scarring
- replacing the skin to prevent further damage like swelling
- chronic wounds

for experimental models
- can develop more treatments based on
- can test the effectiveness of the treatment

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2
Q

function of the skin

A

Protective barrier against the UV,
Thermoregulatory
hormonal - like Vit D
aesthetics

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3
Q

3 layers of the skin structure

A

epidermis - outermost layer
dermis
hypodermis - layer of fat - inner most layer

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4
Q

what does the basal layer so

A

contain stem cells and basal cells which can divide into specialised cells. then they move upwards to the epidermis layer to replace the cells.

Like keratinocytes

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5
Q

what does eccrine gland and secaceous gland do

A

eccrine - produces swear
sebaceous - produces sebum

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6
Q

situations where skin need to be replaced

A

chronic wounds like when there is an ulceration

-recontrsution following a surgery like burns, excision, amputations

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7
Q

when there is a wounds, skin can be left to heal. but sometime a graft is better. why?

A

leaving it to heal will increase the the risk of infection as it may take a long time to heal.

and depending on the site of the wounds, when it heals, the skin will be pulled together to close the wound and it will look weird. So graft is better for cosmetics

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8
Q

example of a graft

A

split skin graft >thin layer of skin from elsewhere.
Composed of epidermis and a superficial part of the dermis

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9
Q

ideal characteristics of bioengineered skin

A

-durable
-semi permeable to wear
-barrier to microbial invasion
-non antigenic
-non toxic
-easy to apply
cosmetically acceptable
painless

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10
Q

what are the current skin substitutes

A

Acellular dermal sub
Autologous epidermal sub
Allogenic epidermical -dermal sub

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11
Q

properties of acellular dermal sub

A

a compostite of consists of a collagen mesh, which acts as a “dermis” and a silicon membrane which acts as an “epidermis

  • has no cells in the sub
  • can be used to cover the wound short term
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12
Q

properties of autologous epidermal sub

A

has autologous keratinocytes on the membrane with laser drilled pore.

Keratinocytes are derived from the cell culture of the biopsy from the patient

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13
Q

properties of allogenic epid-dermal sub

A

keratinocytes are taken neonatally and incoporated into the membrane alongside collagen and fibroblasts

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14
Q

process of tissue regeneration via cell therapy by bone marrow cells

A

Bone marrow cells > isolate the HSC (hematopoitic stem cells

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15
Q

process of tissue regeneration via cell therapy by biopsy

A

biospy> cell isolation of wanted cells like keratinocytes, fibroblast etc > creates cell cultures on them > (two ways for the next step)

Cell culture> tissue engineering to create a graft of biomaterial> transplantation

or

Cell culture > local application of differentiated cells

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16
Q

process of tissue regeneration via cell therapy by iPS

A

biospy> cell isolation of wanted cells like keratinocytes, fibroblast etc > reprogrammed them using transcrption factors into iPS cells

then genome editing on the iPS cells> in vitro differentiation > used to make the graft

17
Q

problems of bioengineered skin

A

lack of differentiated cells included in the skin
- reduced vascularization
- scarring
cell therapy
development costs
- can degrade and affect other biological tissues

18
Q
A