derm A Flashcards

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1
Q

skin- other pathologies

A

psoriasis, dermatitis, infections, toxin exposure
- ~psoriasis: ~8-9 million in US population (chronic inflammatory skin disease –> impact on QOL and skin function)

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2
Q

skin structure and function: barrier has cellular basis?

A

epidermal:
- cell-cell and cell-matrix connections, extracellular lipids.

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3
Q

skin structure and function: Epidermal renewal and repair?

A
  • stem cell replication
  • hyper-proliferative pathologies
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4
Q

skin structure and function: skin adexnal structures?

A
  • hair and sebaceous glands
  • nails
  • sweat glands
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5
Q

skin the reductionist approach: epidermis

A
  • keratinocytes, melanocytes, langerhaan cells. (barrier structure & function from keratinocytes)
  • barrier function is mostly held within the first 2 cell layers in the epidermis (essential)
  • flat cells in the epidermis help barrier function (shape change to flat further towards the surface)
  • keeps germs and toxic shit out.
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6
Q

skin the reductionist approach: dermis

A

extracellular matrix proteins & diverse cell types (blood vessels, glands, nerve endings, base of hair follicles)
- papillae hold layering together
- hypodermis below dermis

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7
Q

Skin- tissue overview

A
  • skin (also known as integument) is the largest organ, variable thickness
  • Composed of two tissue layers: surface (cellular epidermis –> one cell on top of another), lower (mostly acellular dermis –> small amount of fibroblasts but surrounding is made of mostly noncellular material such as collagen, a connective tissue)
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8
Q

skin- epidermal functions

A
  • Protection from physical-chemical trauma, desiccation
  • ~1/10th of entire skin thickness
  • metabolic – synthesis of vitamin D
  • Antigen up-take (langerhans’ cells –> immune system derived) –> there are not a lot of langerhans cells by %, but there are a lot in total because of the large surface area of the epidermis
  • No blood vessels –> nutrients come from blood vessels in the dermis
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9
Q

Skin- Dermal functions

A
  • Sensation: support for nerve endings
  • Blood vessels: nutrient supply for epidermis and dermis thermoregulation via dilation and constriction.
  • blood vessels are larger in the RETICULAR LAYER and are finer capillaries in the PAPILLARY LAYER (more densely packed collagen)

https://o.quizlet.com/KPXA.d-BMVpm3GYX9i4-8w.png

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10
Q

melanocytes: epidermal

A

-melanocytes, MCs (pigment cells) –> skin and hair pigment
- ~5% of epidermal cells
- “clear” cytoplasm –> light in color themselves
- ~1 melanocyte for 10-20 basal keratinocytes
- make melanin (pigment) and ships the pigment off to surrounding cells called keratinocytes
- arborized/dendritic

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11
Q

epidermis- Melanin

A
  • production stimulated by endocrine & paracrine signals at melanocortin receptor
  • delivered to & phagocytized by KCs
  • KCs are packed with intermediate filament protein = keratin
  • partly digested by KC lysosomes
  • accumulates over KC nucleus
  • scatters & absorbs UV light
  • forms a protective cap over the genetic material of keratinocytes to decrease mutations and carcinogenesis of UV light
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12
Q

epidermis - melanin variation in density across body surface

A
  • regional concentration (nevus or “mole”) –> leads to a small group fo keratinocytes with a lot of melanin but still normal/healthy
  • ABCDE’s of moles: asymmetry, border, color, diameter, elevation
  • change may indicate malignancy (dysregulation of melanocytes)
  • ex. smaller than the width of a pencil eraser is usually fine, flatter elevation is less worrying
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13
Q

epidermal pigmentation

A

melanin: 2 types –> skin and hair are a balance of the two
- brown-black, eumelanin
- reddish-yellow, phaeomelanin
- ratio determines pigmentation; eumelanin more photoprotective
- both increase in response to UV light –> melanin production is stimulated by UV light (ex. tanning)
- triggered by MSH (melanocyte-stimulating hormone = melanocortin)
- binding membrane melanocortin receptor
- overall pigmentation –> combination of MSH levels (signal), MSH-receptor activity, melanin production
- freckles = keratinocytes concentrated melanin from melanocytes

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14
Q

epidermal pigmentation - vitiligo

A

localized, progressive loss of pigmentation
- incidence: ~1/100; all races & both sexes are affected
- autoimmune destruction of MCs; associated with other autoimmune diseases, ex. pernicious anemia
- proteins are seen as foreign antigens –> destruction of self-proteins
- deficit of color = MC destroyed

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15
Q

epidermis cell types: langerhans’ cells (LC)

A
  • <5% of cells in epidermal layer
  • bone marrow-derived –> migrate from circulation across basement membrane into epidermis
  • function as part of immune system –> surveillance
  • phagocytize & process low MW antigens (poison ivy/oak) into LCs
  • exposure to antigen triggers migration of LC to regional lymph nodes
  • LC breakdown antigens & present them to other immune cells in lymph nodes (hand off which completes immune response)
  • large surface area of skin provides increased opportunity for antigen detection & initial processing (increases absolute number)
  • ex. allergic reactions)
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16
Q

epidermis cell types: keratinocytes

A
  • ~90-95% of all cells in epidermis
  • upper epidermal layers called stratum corneum show body site specification in response to pressure or friction –> mostly due to changes in thickness of cornified layer (accumulation of cells in the layer)
  • possible “clear layer” –> stratum lucidum (tightly packed squames seen in high frictional stress areas; palms & soles)
  • all sites eventually & normally desquamate –> loss of squames (continual turnover to maintain integrity)
17
Q

epidermis - keratinocyte layers

A
  • basal layer = stratum germinativum
  • spinous layer = stratum spinosum
  • granular layer = stratum granulosum
  • cornified layer = stratum corneum

LOOK AT PICTURE

18
Q

epidermis - keratinocyte basal layer (stratum germinativum)

A
  • mitotic in normal epidermis
  • migrate into wound to cover site
  • the only place with cell replication
  • made of mostly basal cells –> above this layer are postmitotic
19
Q

epidermis - keratinocyte spinous layer (stratum spinosum)

A
  • cells are post-mitotic but still very metabolically active (keratin protein production, etc.)
  • numerous cell-cell attachments = desmosomes –> responsible for “spine-y” histology & much of epidermal structural strength
  • physical connections keep epidermis layer intact
20
Q

epidermis - keratinocyte granular layer (stratum granulosum)

A
  • keratin proteins aggregate (granules)
  • nuclei breakdown; lipids extruded
  • other specialized proteins are chemically x-linked resulting in increased mechanical resistance
  • when cells leave the granular layer they die
21
Q

epidermis - keratinocyte cornified layer (stratum corneum)

A
  • cells cease metabolism
  • cells flatten into discs = squames; eventually lost
  • 3–4 weeks from basal to cornified layer
22
Q

epidermis - structure & differentiation

A

bricks & mortar” (derived from keratinocytes)
- two biochemical phases in granular & cornified layers
- proteins in cells cross-linked together –> hydrophilic “brick” (make up 1 keratinocyte packed with keratin protein)
- lipids in extra-cellular space –-> hydrophobic “mortar” (extrude through cell)
- both are a challenge to transdermal drug delivery but also part of the barrier function of epidermis

23
Q

epidermis: chemical barrier

A
  • slows transit of water-soluble AND lipid-soluble compounds
  • advantages / disadvantages: lessens dehydration of underlying tissue & entry of toxins BUT restricts cutaneous drug delivery
24
Q

epidermis: physical barrier

A

desmosomes between cells provide structural integrity / strength