lect 3- Connective Tissue Flashcards

(41 cards)

1
Q

what are the types of embryonic CT

A

mesoderm, mesenchyme, mucous CT (wharton’s CT)

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2
Q

describe the potency of embryonic CT : mesenchyme

A

totipotent

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3
Q

what cells are located in embryonic Mucous CT

A

fibroblasts and a few mesenchymal cells

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4
Q

what is the major content of embryonic CT

A

mucopolysaccharides

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5
Q

where is loose (areolar) CT primarily found

A

epithelium (site of inflammatory and immune reactions)

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6
Q

define lamina propria (CT)

A

LCT of mucous membranes

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7
Q

where is dense regular CT found

A

tendons, aponeuroses, and ligaments

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8
Q

what is the name for a fibroblasts that is in a tendon

A

tendinocyte

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9
Q

what are the resident cells of the CT

A

fibroblasts/myofibroblasts, macrophages, adipocytes, mast cells

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10
Q

what are the transient cells of the CT

A

lymphocytes, neutrophils, eosinophils, basophils, monocytes, plasma cells

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11
Q

what is the origin for eosinophils, mast cells and basophils

A

CD34+

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12
Q

what immunoglobulin is the surface of mast cells covered in

A

IgE

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13
Q

what do mast cells release

A

histamine, heparin, serine, proteases, leukotrienes

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14
Q

what classes of molecules is the ECM composed of

A

proteoglycans, GAGs, multiadhesive glycoproteins (laminin, fibronectin)

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15
Q

what are the 3 types of fibers of ECM

A

collagen fibers, reticular fibers, elastic fibers

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16
Q

what is the must abundant fiber in our body

A

collagen fibers

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17
Q

describe type 1 collagen

A

skin, bone, tendons and ligaments (resistance to force, tension and stretch)

18
Q

describe type 2 collagen

A

cartilage (hyaline and elastic) (resistance to intermittent pressure)

19
Q

describe type 3 collagen

A

loose CT, forms reticular fibers (supportive scaffolding)

20
Q

describe type 4 collagen

A

basal laminae of epithelia (support and filtration)

21
Q

what is it called when one type of cell because a mature type of another cell

22
Q

what is it called when a mature cell of one type becomes an immature cell of another type

23
Q

what is osteogenesis imperfecta type one a defect in

A

defect in type 1 collagen with normal quality but abnormal quality

24
Q

what are the symptoms of type 1 osteogenesis imperfecta

A

abnormal teeth, blue sclera, brittle bones, progressive hearing loss, repeated fractures, thin skin, weak tendons

25
what is osteogenesis imperfect type 2 a defect in
defect in type 1 collagen with abnormal quality and quantity
26
what are the symptoms of osteogenesis imperfect type 2
severe bone deformities, respiratory complications, intracerebral hemorrhage, 1 year max life span
27
describe kniest dysplasia
defect in type 2 collagen (short stature, ocular changes, wide metaphyses)
28
describe stickler's syndrome
defect in type XI collagen with additional mutation in type 2collagen Gene (craniofacial deformities, retinal detachment, hearing loss)
29
describe ehlers-danlos syndrome
defect in type 3 collagen (hyper flexibility of joints, hyper extensibility of skin, vascular and organ rupture)
30
describe alports syndrome
type 4 collagen pathology (hematuria, progressive hearing loss, ocular lesions)
31
describe thin basement membrane disease
basement membrane less than 260nm in thickness, looks like alports syndrome, quality is normal but quantity is not
32
describe good pasture syndrome
there are auto-antibodies against type 4 collagen, similar to problems with alports, there with be inflammation
33
what type of collagen are reticular fibers composed of
type 3 collagen
34
what stainings are used for reticular fibers
eosin, PAS, silver salts
35
what is involved in the formation of reticular fibers
fibroblasts, smooth muscle cells and Schwann cells
36
what staining is used for elastic fibers
eosin, orcein, resorcin-fuchsin
37
what are elastic fibers produced by
fibroblasts and smooth muscle cells
38
what are the 2 components of elastic fibers
elastin (central core) and fibrillin microfibrils
39
what does fibrillin-1 do
FBN1 gene that organizes elastin into fibers and plays role in Marfan's syndrome
40
describe Marfan's syndrome
mutation of fibrillin gene with a high risk for aortic rupture (tall and thin, long arms/legs, arachnodactyly, chest deformity)
41
what endocrine's function decreases with obesity
adiponectin