Foundations Exam 3 histology Flashcards

(50 cards)

1
Q

What is the protein in the stratum granulosum that aggregates keratin tonofilaments and allows keratinization in more superficial layers

A

Filagrin

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2
Q

Dark brown spots on the surface of the skin is from

A

keratohyaline plaques from over prodiction of keratohyaline granules in the stratum granulosum

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3
Q

eledin is

A

the protein in the stratum lucidium that is thought to be a etabolite of keratohyaline. it makes the stratum lucidium light staining

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4
Q

lamellar bodies are found where

A

in the keratinocytes of the stratum spinosum and granulosum

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5
Q

what do lamllar bodies do?

A

they extrude glycproteins which coat the cell surface

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6
Q

what is psoriasis

A

is it a result of a decrease in the regeneration time fo the epidermis and an increase in mitotic cells in the stratum basale and spinosum. It presents as a patchy red lesion

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7
Q

how do you control psoriasi

A

with corticosteroids

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8
Q

Addisons disease is

A

a lack of cortisol from the adrenal cortex causing overproduction of ACTH leading to pigmentation of the skin

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9
Q

vitiligo

A

genetic mutation leading to degredation and regression of menalocytes and depigmentation

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10
Q

Albinism

A

lack of production of tyrosinase and so they lack melanin

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11
Q

How do you identify a langerhan cell?

A

identify the berbeck granules which are paddle shaped

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12
Q

Langerhan cells are important in

A

delayed hypersensitivity

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13
Q

What does a merckel cell do and where are they found

A

clear cells found in the stratum basale near connective tissue which are involved in Krude touch and in hair folliKles

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14
Q

how do you recognize a merkel cell?

A

have dense secretory vesicles in the cytoplasm

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15
Q

where is blood supply of the epidermis?

A

in the papillary layer of the dermis

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16
Q

Meissner’s

A

In the papillary layer of the dermis and are used for fine touch in hairleSS region. unmyelinated nerve endings and in vibraSSions

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17
Q

Pacinian corpuscle

A

Pressure and vibration in the reticular dermis

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18
Q

Ruffinis corpuscle

A

endings respond to stretch

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19
Q

Krause end bulbs

A

cold and pressure detection

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20
Q

which glands are associated with hair follicles?

A

subaceous glands

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21
Q

subaceous glands strucutre is

A

a branched acinar gland with a short ductal system that release contents in a holocrine fashion

22
Q

which sweat gland is associated with sweat glands?

23
Q

Epidermal Bullosa

A

defects in intermediate filments that anchor the epidermis to the underlying BM

24
Q

Epidermal Bullosa simplex

A

where blistering occurs in the epidermis and basal epidermal cells separate. This is the most common type of EB,and tends to be milder than the other types.

25
junctional epidermolysis bullosa
caused by defects in IFs where blisters form between the dermis and epidermis
26
distropic epidermolysis bullosa
type VII collage mutation resulting in separation of the papillar from the reticular dermis that heals with scarring
27
how do you tell the difference between the basal cell carcinoma and squamous cell carcinoma
the squamous cell is making alot more hyaline and lamellar bodies since they are from more mature kertinocytes
28
The A band is
the length of the myosin molecul in the center. It does not change . microscopically it will appear as a single thick filament surrounded by the thin filaments
29
What does the I band look like microscopically
It will be the thin filaments surrounded by titin
30
titin
extends from the z-line to the H band and anchord the myosin filaments to the Z-line
31
what will the M band look like ?
It will have a myosin thick filament with myomesin holding them together
32
myomesin
holds the myosin filaments in register @ the M line
33
alpha actinin
anchors actin to the Z-lne
34
tropomodulin
caps the free end of actin thus regulating its length
35
costamere
attach myofirils to the sarcolemma at the Z-line
36
Dystrophin
links actin to the sarcolemma and to the lamina of the ECM
37
in Muscular Dystrophy, how is it inherited and what protein is malfunctioning
dystrophin and is X-linked recessive and is assocaited with a replacement of degenerating skeletal muscle with fatty firous connective tissue
38
what s a t-tubule
an invagination of the sarcolemma at the AI j(x) between two terminal cisternae
39
explain the calcium binding in a cell to allow muscle contraction
calcium binds to troponin which undergoes a confrmationl change resulting in the moving of tropomyosin on the actin molecule which exposes the myosin binding sites. now the myosin head can bind to actin
40
myasthenia gravis
autoimmune diease where Abs block Ach receptors of the motor end-plates leading to a gradual weakening
41
botulism inhibits
the release of Ach from the motor end plate
42
the efferents of the spindle fiber are what kind of nerves
gamma motor
43
the extrafusal fibers in the muscle are innervated by
alpha nerves
44
what does MyoD do?
myoblasts epxress it and turn on muscle specific genes
45
what inhibits muscle development
myostatin
46
fascia adherens in cardiac muscle attaches to
skeletal muscle
47
in cardiac muscle where is the t-tubule?
the z-line
48
in smooth muscle what binds to calcium?
caldesmon and calponin
49
what activates myosin in the smooth muscle cells?
Myosin light Chain Kinase
50
what activates the MLCK (myosin light chain kinase?
calcium-calmodulin complex