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33 Cards in this Set
- Front
- Back
phagocytosis
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cell eating
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Phagocytosis occurs mainly in which types of cells?
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mainly in specialized cells like neutrophils and macrophages
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Pinocytosis. in which cells types? ingests what?
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cell drinking=ingestion of solutes such as protein hormones, macromolecule complexes in liquid medium
is prevanlent in all cell types |
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Receptor Mediated Endocytosis (RME) is the ____dependent _____of what?
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clathrin dependent ingestion fo receptor bound material in clathrin-coated pits
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Caveolae is __________ formed by _______ in______
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the ingestion of small vesicles formed by aggregation of Caeolin in lipid rafts
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Macropinocytosis
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uptake of liquid in large vesicles formed by extensions of the plasma
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name the 3 types of pintocytosis
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RME, Caeolae, Macropinocytosis
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Steps of RME
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1) Ligands internalized specifically
2) sorted into clathrin coated pits in membrane 3) budding of pits from Plasma membrance to make clathrin vesicles (requires GTPase=Dynamin to pinch off) |
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Structure of Clathrin.
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chain-link fence/cage/lattice when aggregates.
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Function of Clathrin
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1) distorts plasma membrane by building to produce vesicle
2)capture membrane receptors/bound molecules |
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In Endocytosis, binding of _____and _____creates _______change in opposite part of protein to allow what?
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receptor and ligand creates conformational change in the opposite part of the protein to allow Adaptor Proetin 2 to bind to the specific AA sequence in the cytoplasmic tail domain of the receptor/clathrin coat
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The ligand, receptor, (with trans membrane protein) and Adaptor protein connect to the_____ and get...?
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clathrin cage on the outside of the cell and get sucked into like a black hole
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First step of RME Trafficking: At the Early Endosome...
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clathrin coat dissociates/vesicles fuse with Early Endosome
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Second step of RME Trafficking: early endosome membrane contains _____ that lowers ____ and causes...?
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H+pump that lowers pH of the lumen to 6.0, causing dissocation of the ligand from the receptor and triggers recycling of receptors back to plasma membrane
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Sorting in the Early Endosomes creates 2 types of vesicles that bud from the early endosome. What are they?
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1) transport (recycling) vesicles that carry receptors and membrance back to the plasma membrance
2)endocytic vesicles that carry ligand further on to the late endosome |
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Late Endosomes have pH of ___, fuse with ___ carrying_____ from trans Golgi tagged with ________
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5.5 and fuse with transport vesicles carrying the lysosomal hydrolases from trans Golgi tagged withe Mannose 6Phosphate
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Late Endosomes mature into Lysosomes by...?
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1) sorting hydrolytic enzymes with ligand
2) recycling of endosome membrane proteins back to trans Golgi 3) lower pH to 5.0 for enzyme activation |
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Vesicles are transported along microtubules via...?
which protein goes + and which protein goes - ? |
Dynein motor proteins (towards minus ends of MY) or Kinesins (toward the plus ends of MT)
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Name some examples of Ligands. 9 categories
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1) Hormones: insulin, glucagon, LH, Growth, Prolactin, TSH, TH
2) Growth Factors: Epidermal Growth Factor/Nerve Growth Factor 3) Lipoproteins, LDL, VLDL, HDL 4) Antibodies, IgE, IgG via Fc receptors 5) Vitamins: A,D, B12 6) Iron Binding Proteins: Transferrin 7)Toxins: Diptheria, Cholera 8) Viruses: adenovirus, rous sarcoma |
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In some cases, some growth factor receptors, want to downregulate endocytosis. What does this and how? what is this called?
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MultiVesicular Bodies (MVB)
sort and degrade integral membrane proteins and help hormone desensitization by removing the receptors from the surface of the cell Ex.) EGF-tagged for degradation by Ubiquitin |
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Describe function of Ubiquitin. What happens then?
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Ubiquitin tags receptors to be sorted into small vesicles.
These vesicles bud from the late endosomes, accumulate in MVB, fuse with the lysosome, and are then degraded. Then hormone has less receptors to bind to on cell surface =desensitized |
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Caveolae are a mechanism of what?
Where are they abundant? |
Mechanism of pinocytosis. ARE NOT RECEPTOR MEDIATED!
Abundant in vascular endothlial cells. Smooth muscles cells, fibroblasts and adipocytes. |
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Caveolins are what? Where are they located and what do they help make up?
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Integral membrane proteins anchored into the plasma membrane in rigid lipid rafts, that help to make up caveolae.
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Function of Caveolae:
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1Endocytosis: byd as vesicles from plasma membrane/fuse with “caveosomes/early endosomes.
2) Transcytosis: bud as vesicles from cell surface, traverse the cell and fuse with plasma membrane at another location on cell surface |
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Lysosomes. Describe size, electron density, internal components?
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variable in terms of size. Electron dense but not uniform. Lumen has many different types of Lysomal enzymes/acidic hydrolases.
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Lysosomes have a ____ which is used for activating....?
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proton pump (via ATP) lower pH to 5 for enzyme activation=fully active.
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Glycosylation of membrane proteins in lysosomes serve as _______ to protect membrane against....?
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glycoprotein lining to protect against it's own enzymes along the inner/luminal membrane
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Lysosomes have membrane transporters for...?
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release of digestion products (AA, sugars, lipids). You have to poop it out!
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Formation of Lysosomes: Tag for lysosomal enzymes? binding through ____. Fuses with ______. Low ____ dissociates _____. What is recycled to trans golgi? How do lysosomes become mature? pH?
Draw it out! |
1)Lysosomal enzyme tagged with Mannose 6-P in cis golgi
2)sort through golgi-trans golgi 3) M6Ps are not transmembrane, so have receptors that bind thru membrane to adaptor protein, then clathrin binds 4) clathrin coat sheds and then vesicle Fuses with late endosomes 5) Low pH (5.5) of Late Endosome dissociate M6P recepetors from enzymes 6)M6P receptors recycles back to trans golgi via transport vesicles 7)Late Endosomes mature into Lysosomes by sorting hydrolytic enzymes/lowering pH to 5.0 for enzyme activation |
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Lysomal Storage Diseases
If problem with lysomal enzymes-going to have problem... |
digesting material that cells take up=diseases, especially in Tay Sachs
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Tay Sachs=
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a-Hexosamindidase A =accumulation of GM2 Gangliosides in brain-causes increase in Glial cells and abnormal growth of dendritic processes of neurons.
Mutation can’t break down gangliosides properly = accumulates+disrupts neural system |
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Gaucher’s Disease=
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b-glucocerebrosidase accumulates in macrophages =heptamegaly/enlarged spleen
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I-Cell Disease=
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processing of mannose 6-p tag is defective. Cant sort lysosomal enzymes. Non specific. Lysosomes can’t degrade anything!
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