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hematoxylin
basic dye that stains DNA/RNA
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eosin
acid dye that stains non-DNA/non-RNA cell components
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glutaraldehyde/osmium tetroxide
EM; fixes cells/tissues using heavy metals
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another name for organelles
"small organs"
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another name for cell membrane
plasmalemma
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polar head
glycerol conjugated via a phosphate bridge to a nitrogenous compound such as choline, ehtanolamine or serine
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examples of receptor proteins
adenoreceptor, adenylate cyclase/cAMP system
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examples of adhesion proteins
selectins, integrins, cadherins
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another name for cytoplasm
"matrix": contains organelles, inclusion bodies, cytoskeletal elements (microT, microF, intF)
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lamins
inner mem of nuc env has attachment sites for lamins; filamentous prot; maintain shape and integrity of nuc env (cell division)
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transfer vesicle
btw ER and golgi
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secretory vesicle
- btw golgi and surface
- condenses to form vesicles/granules
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lysosomes/osteoclasts
lysosomes are stored for varying times in osteoclasts/WBC (comparative to secretory granules in other cells)
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constitutive secretion
rapid, continuous; prod do not accumulate w/in cell; few secretory granules
i.e. ECM by fibroblasts
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regulated secretion
episodic, lots secretory granules
i.e. hormone stim secretion of dig enz from pancreas
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acid phosphatase
enz in lysosome
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primary lysosome
hydrolytic enz only
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secondary lysosome
aka phagolysosome; primary lysosome + phagosome; has hydrolytic enz and ingested material being lysed
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tertiary bodies
aka residual; multiple vesicles/membranous mat bounded by mem; older/end stage remnants of secondary lysosomes
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residual bodies
may contain pigmented mat called lipofuscin (aging pigment), which remains in neurons and cardiac muscle cells
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Tay Sach's disease
ex of lysosomal storage disease; hexosaminidase A deficiency results in abnormal accumulation of ganglioside
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peroxisomes
form from sEr and pre-existing peroxisomes; prod H2O2 (toxic to cells) and breaks down H2O2 via catalase
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microbodies
aka peroxisomes
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adrenoleukodystrophy
impaired beta oxidation of fatty acids leads to abnormal lipid storage in CNS and adrenal glands; ex of defect in peroxisomal enz
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proteosome constituents
core particle + regulatory particle
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inclusion bodies
non-mem bound in cytoplasm or nuc; DOES NOT include cytoskeletal elements
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lipid droplet
inclusion body; stores fatty acids as triglycerides (adipose cell, adipocyte)
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glycogen granules
inclusion body; stores glucose as glycogen (liver cell)
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axoneme
9x2+2 of cilia/flagella
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centriole and tubulin relationship
centrioles assoc w/ g-tubuli which is responsible for microT assembly (nucleation)
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nesprin
outer nuc mem prot; mediates microT dep positioning of nuc w/in cell
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nesprin-sun complex
connect to microT via kinesin to the nuc; important in polarized cells w/ specialized functions (i.e. lining columnar cells of SI)
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elementary particle
ETC molecules; anything assoc w/ inner mit matrix
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viblasatine/vincristine
inhibits tubulin polym in cancer cells; loss of microT usage in cell division; derived from plant alkaloid
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colchicine
inhibits tubulin polym and therefore inhib leukocyte migration and phagocytosis and inflammation; derived from plant alkaloids
rxs pain and inflammation assoc w/ gouty arthritis
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microvilli and actin
microF are the linking structural support of microvilli to terminal web
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neutrophils and microF relationship
microF imp in neutrophil migration to areas of inflammation; defects in microF leads to predisposition to bact infection in diseases such as diabetes mellitus
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actin-scaveneger/actin toxicity
actin released from dying cells into ECM and general circulation; leads to hepatic necrosis, septic shock, adult respiratory syndrome and prego disorders; leads to general disruption of platelet func and normal vascular flow
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gelsolin
aka actin-deactivating factor; binds to actin in circulation and disrupts it; reduces actin to G actin + gelsolin
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Group-specific component protein (Gc)
takes G actin + gelsolin complex and binds it to plasmalemma of hepatocytes which take it up for degradation and excretion
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neurofibrillary tangles
alzheimer's; composed of masses of neurofilaments (intF) aka degenerated neurons; also seen in Down's syndrome brains
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CAMs importance
- cell migration in embryogenesis
- holding tissues together in adult
- inflammation/wound healing
- tumor metastasis
- signal transmission
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zonula occludens
"tight junctions"; composed of sealing strands (formed from row of TM prot embedded in both PMs)
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claudins and occludins
zonula occludens prot; anchor tight junctions to intracellular actin (microF)
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zonula occludens func
- hold cells together
- block mvmt of integral mem prot
- prevents passage of mol and ions btw cells
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zonula adherens
"belt juncitons"; epithelial cells
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cadherin, alpha catenin, beta catenin
zonula adherens prot
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cadherin prot family
desmosome, desmoglein, desmocollin
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intF and desmosomes
desmosomes are attached to intracellular keratin or desmin filaments
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desmosome function
resist shearing forces; in simple and stratified squamous epithelium and muscle tissue
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blistering (bullous) diseases
due to misfunctioning desmosomes
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pemphigus vulgaris
blistering disease due to genetic defects in desmosomal prot or autoimmune response
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nexus
aka gap junction; composed of prot complexes (connexons) btw adjacent cells
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acrocentric chrom
p is a nub, 13, 14, 15, 21, 22 chrom
- stalks=secondary constricts, aka NOR
- satellites=chrom distal to stalk
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giemsa, quinicrine
stain banding patterns of chrom
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alpha/beta importin
receptor on prot entering nuc pore
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BRCA 1 prot
reg of cell cycle in nuc; in breast cancer it is in cytoplasm bc mut doesn't allow its transport into nuc; same for p53
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emerin
integral prot w/in inner nuc mem; member of nuclear lamina-assoc prot family
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Dreifuss-Emery MD
X-linked inherited degenerative myopathy resulting from mut in emerin gene
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MPF functions
- condense DNA
- spindle apparatus
- nuc env breakdown
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aneuploid cells
70% of human cancers
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microscopical chrom
first appear in prophase of mitosis
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bivalence of homologous chrom
aka tetrad of four chrom
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maturation division
aka meisosis II
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pseudoautosomal regions
on X and Y chrom; allows pairing bc they are non homologous
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heteropyknosis
aka inactived X chrom
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When does X chrom inactivation occur?
blastocyst stage
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TGF-beta, interferons, TNF
growth inhibiting factors to terminate/inhibit cell division; decreases cyclin levels and affects spindle function
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Robertsonian translocation
involves two acrocentric chrom that fuse near centromeric region w/ loss of short arms...resulting karyotype only has 45 chrom
most common are chrom 13 and 14; phenotypically normal
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Philadelphia chrom
translocation of 9 and 22; CML results
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epithelium derivations
all three germ layers!
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sarcomas
cancer from endothelium and mesothelium
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carcinomas
true epithelial cancers
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stratified vs simple
stratified do not have junctional complexes but do have individual cell junctions such as desmosomes
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plaque
anchoring prot inside epithelial cell that binds to integrins and cytokeratin filaments
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apical surface area
increased by microvilli and stereocilia
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stereocilia
characteristic of epididymis and proximal vas deferens; not motile
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basal infoldings
basal side; has lots mit for energy prod
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sesnsory cilia
provide chemosensation, thermosensation, and mechanosensation of EC env; non-motile
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goblet cell
single cell of exocrine gland
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formed gland
multiple cells of exocrine gland
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merocrine secretion
aka eccrine; exocytosis; i.e. ant pit secretion of TSH
serous, mucous, seromucous
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apocrine secretion
release of secretory inclusions and granules w/ small amt of apical cytoplasm and cell mem; i.e. mammary gland secretion of lipids in milk prod
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holocrine secretion
secretory prod retained w/in cell which dies; then entire cell w/ prod is released
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