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58 Cards in this Set
- Front
- Back
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What is epithelium?
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Avascular tissue on exterior of body and lines cavities. Functional component of glands.
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Epithelial cell characteristics
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free apical; latter cell-cell adhesions; polarity; on basement membrane
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Epithelioid tissue
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like epithelium but lacks free apical surface
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Functions of epithelium
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Transport; Absorption; Secretion; Protection; Receptor
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Classify epithelium
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1. layers (simple, stratified) 2. shape (squamous, cuboidal, columnar) 3. apical specializations (microvilli, stereocilli, cilli)
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Epthelial dysplasia (1 of 11)
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In response to persistant injury. Regresses. Histologically-increase in nucleus size; abnormal arrangement of cells. Usually in hyperplastic squamous epi. (skin, bronchus, cervix)
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Carcinoma (2 of 11)
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Arises from epi. cells but invades surrounding tissues. Malignant changes but no invasion thru basement membrane. Name by appearance, cell origin, or organ of development.
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Microvilli
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Core of actin filaments (MF) inserts into terminal web. Increase surface area.; Actin binding proteins (ABPs)= villin (at tip), fimbrin, fascin, myosin 1 (anchor to lateral), myosin 2 (terminal web)
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Stereocillia
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Long microvilli ONLY in epididymis, ductus deferens, hair cells of ear; ABPs=erzin, fimbrin, alpha-actinin (terminal web)
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Cillia (flagella)
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Core of MT arranged into axoneme. Types- motile and nonmotile (AKA primary)
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Motile cilia
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9X2 microtubules. Outer doublet is a complete A MT and incomplete B MT. Dynein arms of A MT slide along B MT (uses ATP). Dynein allows cilium to bend. Radial spokes regulate ATPase.
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Primary Ciliary dyskinesia (immotile cilia syndrome) (3 of 11)
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Group of autosomal recessive hereditary disorders. Kartagener's syndrom- no dynein arms, respiratory infections, sterility, situs inversus in 50%. Young's syndrome-no radial spokes, same symptoms
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Nonmotile (primary) cilia
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One/cell. Axoneme with 9+0 MTs. Sensory-kidney epithelia.
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Polycystic kidney disease (4 of 11)
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4th cause of kidney failure. Defect in sensory cilia of collecting ducts. Urine bends cilia and opens calcium channel for signal transduction pathway. Formation of cysts.
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Basal body (centriole)
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At base of cilia and template for ciliary formation. If at nucleus it is a centriole. 9 sets of triplet MTs (A,B, and C). Found in pairs at right angles.
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Bardet-Biedl Syndrome
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Group of genetically heterogeneous disorder. Defect in basal bodies or cilia causes no signaling pathway. Retinal degeneration, etc. Kidney transplate if becomes cystic.
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Endothelium
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simple squamous epi. lining vascular system
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Mesothelium
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simple squamous epi. lining walls and closed cavities
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Pleural mesothelioma (6 of 11)
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Tumors in parietal and visceral serous membranes. Caused by exposure to asbestos and long latency period.
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Pseudostratified epithelium
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appears stratified but all cells on basement membrane
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Transitional epithelium
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stratified squamous epi lines lower urinary tract
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Junctional complexes (terminal bars)
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adhesive components between epi cells; consist of zonula occludens, zonula adherens, macula adherens
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Zonula occludens (tight junction)
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Most apical. Limited resistance to mechanical stress. Transmembrane proteins: claudins (sealing), occludin (signal transmitter), junctional adhesion molecule (intx w/claudin), ZO-1 (intx w/actin). Transports and establishes barrier to restrict diffusion. MFs, almost fused cm; Paracellular
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Claudins
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transmembrane protein of z. occludens; backbone of strands; seals; forms extracellular aqueous channel for paracellular transport; claudin 1=coreceptor for Hep C; claudin 4=recept for Clostridium p. exterotoxin, drugs
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Occludin
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transmembrane protein of z. occludens; signal transducer; tumor suppressor; regulates actin and pore permeability
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Junctional adhesion molecule (JAM)
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transmembrane protein of z. occludens; associates with claudins; binds retroviruses, coxsackie, adenovirus
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Destruction of junctional complexes: bacteria (7 of 11)
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Bacteria targets proteins of z. occludens so it breaks down. Enterotoxin of Clostridium perfrigens binds claudins and porms a pore. H. pylori binds to JAM at tight junctions and loss of polarization.
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Destruction of junctional complexes: viruses (8 of 11)
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Virus targets protein of z. occludens causing cancer of death. Hep C binds claudin and internalizes. Retroviruses bind Jam and internalize. Parasites have serine protease that destroys ZO.
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Cell adhesion molecules (CAM)
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Transmembrane proteins. Interact with each other by extracellular domains. Low strength adhesion. Interact with cellular cytoskeleton by cytoplasmic domains.
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Zonula adherens
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Band around cell. Strong cell-cell interaction. E-Cadherin (Ca dependent) to interact with actin cytoskeleton via ABPs
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Fascia adherens
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Adheres cardiac muscle cells. Similar composition to z. adherens.
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Macula adherens (desmosome)
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Major; strong attachment. Anchoring sites for Ifs- keratin (tonofilaments). Not continuous band. Also outside of junct complex
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Desmosomal attachement plaque
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Electron-dense disc on cytoplasmic side of each cell. Where IFs are anchored. Dissipating physical forces. Composed of desmoplakins and plakoglobins.
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Communicating (gap) junctions (or nexus)
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Direct passage of signaling molecules. In epi, sm muscle, cardiac muscle, nerve. Transmembrane channels. Low electrical resistance. Connexon with 6 sym subunits of connexins. Channel regulated by Ca-induced changes in connexin.
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Mutations in connexin genes (9 of 11)
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Cx26 congenital deafness (K circulation in cochlear). Cx46 & Cx50 inherited cataractss. Cx32 associated with X-liked Charcot Marie Tooth Disease ( peripheral neuropathy)
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Basement membrane (LM) / Basal lamina (EM)
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Acellular layer of BL, reticular lamin, and anchoring fibrils. Collagen type IV, laminin (initiates assembly of basal lamina), proteogylcans, glycoproteins. Reticular lamina (type III collagen). Anchoring fibrils- type VII collagen anchors BL to reticular lamina. Interacts with fibronectin
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BL appearance in EM
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1. Lamina densa- type IV collagen, laminins, proteoglycans, glycoproteins, electron dense. 2. Lamina rara (lucida)- artifact, clear area
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Type IV collagen
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3 domains: N-terminal 7S; middle helical, C-terminal NC1. Form NC1 trimer using 3 NC1. Form NC1 hexamer by interaction of 2 NC1. Tetramer by interaction of 4 dimers by 7S. Suprastructure by end-to-end interaction of tetramers.
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BL molecules
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Entactin-links laminin with type IV collagen. Perlecan- proteoglycan with protein core and heparan sulfate
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Self-assembly of BL
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Initiated by IV collagen and laminins. Ca dependent and polymerization of laminin of basal surface. Type IV collagen associates with laminin using entactin. This provides binding sites for other mlc. Integrin binds to laminin.
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Hemidesmosome
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Where lots of mechanical stress. Intracellular attachment plaque.
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Bullous pemphigoid (Blistering disease) (10 of 11)
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Autoimmune disease-Ab against hemidesmosomes. Presence of IgG against BP230.
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Focal adhesions
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Anchors actin filaments into BL (by integrins via ABPs). Dynamic changes of epi cells (wound healing). Also in fibroblasts and sm. muscle. Site of signal dectection and transduction. Integrins bind to fibronectin and laminin.
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Infoldings of basal CM
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In fluid-transporting cells. Increase surface area dn where mitochondria are concentrated.
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Glands
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Epithelial origin. Proliferation of epi cells and invagination into CT.
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Endocrine
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no duct system; hormone secretes into CT and enters blood to travel to target
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Paracrine
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no duct system; secretes into extracellular space and diffuse thru CT to affect cells with same epi.
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Exocrine
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Secretes onto epi surface or by duct. 1. merocrine (eccrine) is release by exocytosis, salivary gland 2. apocrine- release along with entire apex of cell, mammary 2. holocrine-whole cell released, sweat
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Exocrine glands by number
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Unicellular- single cells among non-secretory. Multicellular- more than one cell
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Serous gland
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proteinacious, water, round/oval nucleus
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Mucous gland
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Mucins, flat nucleus against BL
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Mixed gland
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Both serous and mucous cells. Serous and base of acinus outside mucous called serous demilunes.
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Stroma
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CT component; encapsulates, divide, barrier, innervation, myoepithelial cells
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Parenchyma
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functional component; secretory cells and ducts
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Adenocarcinoma (11 of 11)
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originates in glandular tissue; not necessarily glandular but are secretory
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ectoderm
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surface ectoderm; anterior lobe of pituitary; neuroectoderm
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mesodermal
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epi of kidney/gonads; mesothelium (lining of pleural and peritonial); endothelium (line CV vessels); adrenal coretex, epi of genital
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endodermal
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epi of respiratory and GI; epi of thyroid, parathyroid, thymus
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