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4 types of tissues
epithelium, connective, muscle and nervous
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basement membrane parts
basal lamina and reticular lamina
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lamina lucida
location
composition
- -located b/t the basal side of the cell and the lamina densa
- -made mostly of glycoproteins(laminin and entactin) as well as transmembrane proteins(integrins and dystroglycans)
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lamina densa
locale
composition and function
- -b/t lamina lucida and reticular lamina
- -Collagen 4, coated with proteoglycans(perlacean, which has lots of HepSO4, a GAG)
- -Coll 4= filter
- -HepSO4= negative charges restricts neg charged molecules
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lamina reticularis
- -Collagen 3 (reticular fibers)
- -part of the basement membrane made by FIBROBLASTS, which make fibronectin
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anchoring fibrils
- -Collagen 7
- -attach basal lamina to the lamina retiularis
- made by FIBROBLAST
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microfibrils
- -attach basal lamina to elastic fibers
- made by FIBROBLAST
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laminin
- -part of the lamina lucida
- -has binding sites for Coll 4, HepSO4 and integrins (of epithelial cells and anchor PM of cell to the basal lamina
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Duchennes muscular dystophy
- absense of dystrophin leading to muscular weakness
- -dystrophin binds EC laminin and IC actin filaments
- - MALES ONLY (located on X chr)
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dystrophic epidermolysis bullosa
- -mutation of Coll 7 gene
- -causes defective anchorig fibrils
- -presents as erosion in flexural creases, subepdermal blistering at lamina lucida level
- -in scarring types, blisters are beneath lamina densa
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Pseudostatified columnar epithelia
- trachea- ciliated PCE with goblet cells
- epididymis- PCE with stereocilia
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stereocilia
- -long microvilli
- - increase absoption by increasing surface area
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Kartageners syndrome
- -'immotile cilia syndrome'
- -absent dynein arms in cilia, resulting in immotile cilia which causes respiratory problems and male infetility
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nexin
an elastic protein that connects adjacent MT doublets in cilia
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radial spokes
connect subunit A (of a preipheral doublet) to the central sheath in a cilia
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terminal bars
- -where epithelial cells are held together at their apical ends
- -composed of 3 groups: Occluding (impermaeble), Anchoring (adhering) and communicating
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Occluding junctions
- (1)zonula occludens/tight junctions
- -made up of TMP OCCLUDINS and CLAUDINS which are attched to actin filaments via ZO-1 (ZONULA CYTOPLASMIC PROTEINS)
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anchoring junctions
(2)zonula adherens, (3)macula adherens (desmosome)
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communicating junctions
gap junction- direct cell to cell communications
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cytomegalovirus and cholera toxins
act on occluding junctions resulting in permeable junctions
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C. perfringes
attacks zonula occludens in GIT causing massinve fluid movement into the lumen
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H. pylori
targets ZO-1 and JAM of zonula occludens in the stomach, giving gastric ulcers
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Cholera toxin
- attacks ZO-1 and ZO-2 of zonula occludens
- -also permanently activates Gs in cell, leading to increase cAMP, which leads to diarrhea
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Dust mite
inhaled fecal pellats cause zonula occluden junction breakdown in the respiratory epithelim exposing lungs to allergans
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zonula adherens
- -continuous adhesive band that encirlce and hold cells together with a space of 15-20nm between calls
- -tmp E-CADHERINS bind with e/o on EC side, held together be a Ca++
- -IC- CATENIN, VINCULIN and ALPHA-ACTININ bind them to terminal web and actinin
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desomosome
- -localized sheer resistant 'spot welds'
- - IC disc- made of DESMOPLAKINS and PAKOGLOBINS which anchor to IF of cytokeratin
- -EC interlocking fingers made of Ca++ dependent DESMOCOLLINS and DESOMGLEINS, with a large space b/t cells= 30 nm
- - located in simple spithelia and stratified squamous
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pemphigus vulgaris
autoIg produced against desomsoma; proteins resulting in blistering
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gap junctions
location
composition
function
- -epithelia, CM and SM and neurons
- - 6 transmembrane 'connexins'= 1 connexon, that has a 2nm channel
- -open (dec pH or inc [Ca++]ic)
- -adjacent cells are only 2 nm apart
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focal adhesion
anchor actin filaments of cytoskeleton to the basement membrane
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hemidesomosomes
anchor IF to basement membrane
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intergrins
transmembrane proteins of the basal membrane
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DICT
- mostly Coll 1
- fibers arranged in multiple directions
- few cells and little ground substance
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DRCT
- Coll 1 in parrallel bundles
- form ligaments etc
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aponeuroses
- broad flat tendons with mulitple layes aranged at 90 degrees to adjacent layer
- ** this arrangement is also found in the cornea**
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fibrils
- composed of tropocollagen molecules(3 alpha helix to form a triple helix) and make up fibers
- -stain with osmium and exhibit a transverse banding pattern
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collagen types
- 1- LCT and DCT, bone and dentine
- 2- hyaline and elastic cartilage (only form fibers)
- 3- reticular fibers (only forms fibers and fibrils)
- 4- basal lamina (densa) ONLY, (PRODUCED BY EPITHELIAL CELLS), keeps registration peptides
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AA in collagen and their percentages
- gly-34
- pro-12
- hyp-10
- characteristic aa are hyp and hyl
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registration peptides
on ends of procollagen that are essential for triple helix formation and keep the protein SOLUBLE inside the cell
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tropocollagen
- procollagen - reg. peptides = tropocollagen (insol)
- lys and hyl are cross-linked in adjacent tropocollagens
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reticular fibers
c type
structure
cell types
healing
staining
- -Coll 3, supportive meshwork
- -DO NOT FORM BUNDLES
- -produced by fibroblast, reticular cells and muscle cells(in vessels)
- -placed first in wound healing then replaced by Coll 1
- - PAS stains black b/c Ag loving
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epithelial reticular cells in IS
- Thymus has no reticular fibers
- -have cytoplasmic extensions that make up supportive structure (octopus)
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Ehlers-Danlos type 4
defeciency in Coll 3 causing ruptures in arteries and LI, also characteristic stretchy skin
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elasatic fibers
compostition
proteins
- -elastin core in a sheath of fibrillin microfilaments
- -elastin (gly and hyp rich, hyp poor, hyl absent) NOT COLLAGEN
- fibrillin- organizing center (glycoprotein), sensitive to UV radiation
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elastogenesis
absense of microfibrils during this process results in formation of elastin sheets (lamellae) as seen in the aorta
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desmosime and isodesmosime
hold together elastic chains by cross linking lys residues, makeing it 5 x more extensible than rubber
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Marfan syndrome
mutation of fibrillin gene, a CT disorder, can cause arterial rupture due to only elastic sheet production and no fibrillin to hold
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ground substance
- composed of GAGs, proteoglycans and multiadhesive glycoproteins
- -act as microorganism barrier
- -permits diffusion
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HLA
- -NO SO4
- -forms long chains that many proteoglycans will bind (noncovalently), which will attract Na+ and H2O
- -MADE IN THE PLASMA MEMBRANE
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GAGs
- -long straight polysaccharides of reapeating dissach.
- - amino sugar, uronic acid sugar (which has carboxyl)
- - high neg charge, which cause staining with basic dyes
- - high neg charge attracts Na+ and H2O= gel
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7 types of GAGs
- **All SO4ed GAGs link to a proteoglycan core**
- HLA
- Chondroitin 4-SO4
- Chondroitin 6-SO4
- Dermatan SO4
- Keraten SO4
- Heparan SO4
- Heparin
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syndecan
proteoglycan that links cells to EC matrix molecules
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proteoglycans
- present in all ground substance and on the surface of many cell types
- - can act as binding sites for GF and other signalling molecules
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aggrecan
- proteoglycan with >200 GAGs, chondroitin SO4 and keratan SO4
- -**abundant in GS of cartilage and absorb lots of H2) giving it good resistance to compression**
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Decorin
proteoglycan with only a single GAG
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syndecan
a transmembrane proteoglycan
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multiadhesive glycoporteins
stabalize ECM by binding cell surface, collagen, proteoglycans and GAGs
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fibronectin
main molecule in CT (dimer)
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hyaluronidase
- secreted by S. aureus
- chops HLA in smaller pieces making it soluble and breaking down the ground substance, aiding rapid spread
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fixed CT cells
fibroblasts, macrophage, mast and adipose cells
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myofibroblast
- feature of fibroblasts and SM cells
- found in wound healing (wound contraction) and the preiodontal ligament
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plasma cell
- b cell derived
- -'clock face arrangement' due to alternating patches of hetero- and euchromatin
- -life span of 20-30 days
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Ca++ dependent binding
- -E-cadherins in the Zonula adherans
- -TMP that bind plaques to desmoplakins and apkoglobins of the desmosome (macula adherans)
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transport systems in the neuron
anterograde(via kinesin): fast- synaptic vesicles, med- mtch, slow- proteins and actin
retrograde(vi dynesin)- fast- anything that needs to be degraded
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GFAP
- glial fibrillar acidic protein
- -unique to astrocytes (the largest of the glial cells)
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