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58 Cards in this Set

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What is epithelium?
Avascular tissue on exterior of body and lines cavities. Functional component of glands.
Epithelial cell characteristics
free apical; latter cell-cell adhesions; polarity; on basement membrane
Epithelioid tissue
like epithelium but lacks free apical surface
Functions of epithelium
Transport; Absorption; Secretion; Protection; Receptor
Classify epithelium
1. layers (simple, stratified) 2. shape (squamous, cuboidal, columnar) 3. apical specializations (microvilli, stereocilli, cilli)
Epthelial dysplasia (1 of 11)
In response to persistant injury. Regresses. Histologically-increase in nucleus size; abnormal arrangement of cells. Usually in hyperplastic squamous epi. (skin, bronchus, cervix)
Carcinoma (2 of 11)
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.
Microvilli
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)
Stereocillia
Long microvilli ONLY in epididymis, ductus deferens, hair cells of ear; ABPs=erzin, fimbrin, alpha-actinin (terminal web)
Cillia (flagella)
Core of MT arranged into axoneme. Types- motile and nonmotile (AKA primary)
Motile cilia
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.
Primary Ciliary dyskinesia (immotile cilia syndrome) (3 of 11)
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
Nonmotile (primary) cilia
One/cell. Axoneme with 9+0 MTs. Sensory-kidney epithelia.
Polycystic kidney disease (4 of 11)
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.
Basal body (centriole)
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.
Bardet-Biedl Syndrome
Group of genetically heterogeneous disorder. Defect in basal bodies or cilia causes no signaling pathway. Retinal degeneration, etc. Kidney transplate if becomes cystic.
Endothelium
simple squamous epi. lining vascular system
Mesothelium
simple squamous epi. lining walls and closed cavities
Pleural mesothelioma (6 of 11)
Tumors in parietal and visceral serous membranes. Caused by exposure to asbestos and long latency period.
Pseudostratified epithelium
appears stratified but all cells on basement membrane
Transitional epithelium
stratified squamous epi lines lower urinary tract
Junctional complexes (terminal bars)
adhesive components between epi cells; consist of zonula occludens, zonula adherens, macula adherens
Zonula occludens (tight junction)
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
Claudins
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
Occludin
transmembrane protein of z. occludens; signal transducer; tumor suppressor; regulates actin and pore permeability
Junctional adhesion molecule (JAM)
transmembrane protein of z. occludens; associates with claudins; binds retroviruses, coxsackie, adenovirus
Destruction of junctional complexes: bacteria (7 of 11)
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.
Destruction of junctional complexes: viruses (8 of 11)
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.
Cell adhesion molecules (CAM)
Transmembrane proteins. Interact with each other by extracellular domains. Low strength adhesion. Interact with cellular cytoskeleton by cytoplasmic domains.
Zonula adherens
Band around cell. Strong cell-cell interaction. E-Cadherin (Ca dependent) to interact with actin cytoskeleton via ABPs
Fascia adherens
Adheres cardiac muscle cells. Similar composition to z. adherens.
Macula adherens (desmosome)
Major; strong attachment. Anchoring sites for Ifs- keratin (tonofilaments). Not continuous band. Also outside of junct complex
Desmosomal attachement plaque
Electron-dense disc on cytoplasmic side of each cell. Where IFs are anchored. Dissipating physical forces. Composed of desmoplakins and plakoglobins.
Communicating (gap) junctions (or nexus)
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.
Mutations in connexin genes (9 of 11)
Cx26 congenital deafness (K circulation in cochlear). Cx46 & Cx50 inherited cataractss. Cx32 associated with X-liked Charcot Marie Tooth Disease ( peripheral neuropathy)
Basement membrane (LM) / Basal lamina (EM)
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
BL appearance in EM
1. Lamina densa- type IV collagen, laminins, proteoglycans, glycoproteins, electron dense. 2. Lamina rara (lucida)- artifact, clear area
Type IV collagen
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.
BL molecules
Entactin-links laminin with type IV collagen. Perlecan- proteoglycan with protein core and heparan sulfate
Self-assembly of BL
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.
Hemidesmosome
Where lots of mechanical stress. Intracellular attachment plaque.
Bullous pemphigoid (Blistering disease) (10 of 11)
Autoimmune disease-Ab against hemidesmosomes. Presence of IgG against BP230.
Focal adhesions
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.
Infoldings of basal CM
In fluid-transporting cells. Increase surface area dn where mitochondria are concentrated.
Glands
Epithelial origin. Proliferation of epi cells and invagination into CT.
Endocrine
no duct system; hormone secretes into CT and enters blood to travel to target
Paracrine
no duct system; secretes into extracellular space and diffuse thru CT to affect cells with same epi.
Exocrine
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
Exocrine glands by number
Unicellular- single cells among non-secretory. Multicellular- more than one cell
Serous gland
proteinacious, water, round/oval nucleus
Mucous gland
Mucins, flat nucleus against BL
Mixed gland
Both serous and mucous cells. Serous and base of acinus outside mucous called serous demilunes.
Stroma
CT component; encapsulates, divide, barrier, innervation, myoepithelial cells
Parenchyma
functional component; secretory cells and ducts
Adenocarcinoma (11 of 11)
originates in glandular tissue; not necessarily glandular but are secretory
ectoderm
surface ectoderm; anterior lobe of pituitary; neuroectoderm
mesodermal
epi of kidney/gonads; mesothelium (lining of pleural and peritonial); endothelium (line CV vessels); adrenal coretex, epi of genital
endodermal
epi of respiratory and GI; epi of thyroid, parathyroid, thymus