Connective Flashcards

0
Q

Structure of ground substance

A

Hydrated gel, proteoglycans with GAGs bound to hyaluronan

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1
Q

Type IV collagen proteins

A

Laminin and fibronectin

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2
Q

Structure of GAG

A

Glycosaminoglycans - disaccharides covalently bound to core proteoglycan (like bristle brush)

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3
Q

Characteristics of loose CT

A

Lots of cells, lots of ground substance, few fibers, IRREGULAR

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4
Q

Characteristics of dense CT

A

Fewer cells, less ground substance, more fibers, more organization

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5
Q

Location of mucous CT

A

Only in embryonic/fetal in umbilical cord

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6
Q

Functions of adipose tissue (5)

A

Padding, insulation, energy, endocrine (leptin), heat production (brown)

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7
Q

White vs brown fat

A

Unilocular vs multilocular (foamy), brown more vascular, more mitochondria

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8
Q

Locations of macrophages

A

Live in connective tissue - ie kupffer in liver, Langerhans in skin, osteoclasts in bone

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9
Q

Development of macrophages

A

Bone marrow -> blood (monocytes) -> migrate into tissue

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10
Q

Types of wandering CT cells

A

Macrophages, mast cells, plasma cells, leukocytes

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11
Q

Characteristics of mononuclear and macrophage cells

A

Phagocytosis, lots of lysosomes, antigen presentation

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12
Q

Mast cell physiology

A

IgE, causes degranulation of metachromatic -> histamine and immune reaction

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13
Q

Development of plasma cell

A

B cell that is activated to produce and antibody

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14
Q

Appearance of plasma cell

A

Nucleus to one side (eccentric), large Golgi and rough ER (basophilic), “clock faced nucleus” dt lots of heterochromatin

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15
Q

Origin of CT cells

A

Mesenchyme (pluripotential cells), most mesoderm but not all

16
Q

Function of fibroblasts

A

Produce ECM, remodel and repair, not generally active after development

17
Q

Appearance of fibroblasts

A

Small, dense nucleus, no cytoplasm, surrounded by collagen

18
Q

Active vs inactive fibroblast

A

Active has cytoplasm, processes, rough ER, is actively producing ECM

19
Q

Type I collagen

A

Most abundant, visible fibers, dermis, tendons, ECM, bone, ligaments

20
Q

Type II collagen

A

Cartilage, smaller fibers

21
Q

Type III collagen

A

Reticular fibers, in organ stroma

22
Q

Type IV collagen

A

Basement membranes, lacy

23
Q

Formation of collagen

A

In cell - hydroxylization, glycoslyation, form triple helix (procollagen)
Outside cell - cleavage of peptides (tropocollagen), form into fibrils and fiber

24
Q

Appearance of collagen fibers

A

Striped due to gaps between molecules

25
Q

Connection of Vitamin C to collagen

A

Required for hydroxylization and lysine oxidation

26
Q

Diseases of collagen

A

Ehlers-Danlos, scury, osteogenesis imperfecta

27
Q

Structure of elastin fibers

A

Elastin surrounded by fibrillin microfibrils

28
Q

Marfan syndrome

A

Fibrillin deficiency, causes bone and joint stretching, aortic problems, eye problems