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47 Cards in this Set
- Front
- Back
part of the cell external to the nucleus, suspends organelles and inclusions
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cytoplasm
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portion of the cytoplasm devoid of organelles and inclusions
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cytoplasmic matrix
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types of cytoplasmic inclusions:
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Stored foods
-Glycogen -Fat Pigments -exogenous pigments -endogenous pigments |
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glycogen: found in, demonstrated by, clinical significance
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-liver and striated muscle cells
-PAS reaction -glycogen storage diseases |
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fat (lipid) droplets: found in, clinical significance
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-adipocytes, hepatocytes, muscle, steroid-secreting cells
-accumulate in lipid storage diseases and fatty liver |
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types of exogenous pigments
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-carotene
-inhaled dust (carbon) |
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fat-soluble pigment that imparts a yellow-orange color
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carotene
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types of endogenous pigments
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-hemoglobin
-hemosiderin -bilirubin -melanin -lipofuscin |
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hemosiderin: composition, color, location, clinical relavance
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-iron containing pigment
-brown color -found in macrophages in the spleen and liver -hemosiderosis, hemochromatosis |
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hemosiderosis seen in:
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-increased absorption of iron in diet
-impaired use of iron by body -hemolytic anemias -transfusions |
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types of exogenous pigments
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-carotene
-inhaled dust (carbon) |
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fat-soluble pigment that imparts a yellow-orange color
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carotene
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types of endogenous pigments
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-hemoglobin
-hemosiderin -bilirubin -melanin -lipofuscin |
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hemosiderin: composition, color, location, clinical relavance
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-iron containing pigment
-brown color -found in macrophages in the spleen and liver -hemosiderosis, hemochromatosis |
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hemosiderosis seen in:
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-increased absorption of iron in diet
-impaired use of iron by body -hemolytic anemias -transfusions |
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a more severe accumulation of iron due to a genetic defect resulting in excessive iron absorption or transfusion
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hemochromatosis
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bilirubin: composition, clinical significance
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-yellow-brown pigment
-elevated in liver and biliary disease -skin and sclera appear yellow (jaundice/icterus) |
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types of melanin
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-eumelanin
-neuromelanin -phaeomelanin |
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eumelanin: color, location, clinical significance
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-brown-black pigment
-found in membrane-limited granules in epidermis and pigment layer of retina -increased production in response to UV light -increased in Addison's disease in response to ACTH -absent in albinos (tyrosinase) |
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neuromelanin: color, location, clinical significance
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-black-brown color
-found in neurons, brain (substantia nigra and locus coeruleus) -putative neuroprotective function |
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paeomelanin: color, location, clinical significance
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-red-yellow pigment
-red hair color -not protective against UV radiation |
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Lipofuscin: color, location, clinical significance
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-brownish-yellow pigment in an amalgam of lipids, metals, and organic molecules
-accumulates in long lived cells (neurons, cardiac and skeletal muscles) -accumulation is a measure of cellular stress |
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the dynamic organelle that separates the cell's interanal environment from its external environment
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plasmalemma
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lipid bilayer contains which types of lipids:
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-phospholipids
-glycolipids -cholesterol |
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cholesterol function in the lipid bilayer:
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-strenghtens the lipid bilayer and makes it less deformable
-makes it less permeable to small water-soluble molecules |
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small areas in membranes where sphingolipids and cholesterol are cheifly concentrated
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lipid raft
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lipid raft function:
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-involved in cell signaling (apoptosis and proliferation)
-thicker and molecularly unique from the rest of the membrane, causing proteins to aggregate |
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lipid raft clinical significance
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-some cancer cells have higher cholesterol concentrations->more lipid rafts
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a cholesterol inhibitor that induces apoptosis by reducing raft formation
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simvastatin
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reduction in lipid raft numbers causes:
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downregulation of Akt, cell survival signaling molecule
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types of membrane proteins
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-peripheral
-integral |
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protein that can be removed from the plasmalemma with salt solutions
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peripheral
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protein that is either partially embedded or extends the entire thickness of the plasmalemma
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integral
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protein that extends through the entire thickness of the membrane
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transmembrane
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disease that occurs when normal PrP located on the outer surface of the plasmalemma of neurons is converted to an abnormal variant
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Creutzfeldt-Jacob disease
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Creutzfeldt-Jacob disease variant form mode of action:
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-variant forms cross-linked filaments ->resistant to proteolysis
-accelerates conversion of normal PrP to variant form -normal PrP may have antioxidant function (memory formation?) |
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transmembrane protein clinical relevance:
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-beta-amyloid precurson protein in Alzheimer's
-protein aggregate that forms is resistant to proteolysis |
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importance of beta-amyloid precursor protein
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-neuronal migration during development
-synaptic formation and repair -cell signaling -long-term potentiation of memory -cell adhesion |
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protein causing cancer cells to become resistant to cytotoxic drugs
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multidrug-resistance protein (MDR-1)
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function of MDR-1
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pump cytotoxic agents out of cell (ATP-dependent)
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transports conjugated bilirubin into canaliculi
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MDR-2
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MDR-2 is defective in which disorder
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Dubin-Johnson syndrome
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aquaporin-2 expressed by
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renal collecting tubule cells for water reabsorption
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causes translocation of aquaporin receptors to the the plasma membrane of the collecting tubule cell
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vasopressin
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disease that occurs when both aquaporin-2 genes are inactivated by mutations
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neprogenic diabetes insipidus
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functions of proteins
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-receptors
-transport of chemicals across the cell membrane -enzymatic control of chem rxns at cells apical domain -linker proteins for structural support -cellular identification tags (antigens) -anchor cell to ECM -intercellular junction complexes |
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example of enzymatic control of chemical reactions on cells apical domain
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digestive enzymes on epithelial cells of small intestine
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