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50 Cards in this Set
- Front
- Back
classifications of lysosomes
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primary - newly generated, no digestion
secondary - primary lysosome + vesicle tertiary - aka residual body - seen in long lived cells like neurons |
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LAMP 2
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lysosomal membrane protein - protected from digestion by glycosylation
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constitutive secretory pathway
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vesicle buds off Golgi, gets clathrin coated at the plasma membrane, brings substances in via endocytosis and fuse with early endosomes
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Golgi derived coated vesicle pathway
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coated vesicles bud off directly from Golgi and fuse with an early or late endosome
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mannose 6 phosphate pathway
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marker is in the cis Golgi, it binds to receptor in the TGN. Cargo is moved into a clathrin coated vesicle - fuse with late endosomes and receptor is recycled
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Tay Sachs Disease
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mutated hexosaminidase A --> accumulate ganglioside GM2 in concentric layered structures --> dementia and blindness
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Hurler Syndrome
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deficient alpha L iduronidase --> lysosomes accumulate dermatan sulfate --> affects nervous and skeletal systems
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Gaucher Disease
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beta glucocerebrosidase can't interact with LIMP 2 - glucosyl ceramide accumulates, affecting liver and spleen
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microautophagy
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lysosome itself does pinocytosis
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chaperone mediated autophagy
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target proteins selectively with HSC70 and LAMP 2A as a receptor
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mTOR
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protein that is present when there are plenty nutrients present in the cell - otherwise ribosomes are sacrified during starvation conditions
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proteosomes
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barrel like structures lined with proteolytic enzymes
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ubiquitin
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tags proteins for destruction in proteosomes
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velcade
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inhibitor of proteosomes
treatment for multiple myeloma - allow protein to build up in cancer cells so they die |
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peroxisome
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responsible for beta oxidation of long chain fatty acids (c18+)
also synthesizes phospholipids - plasmalogens needed for myelination of nerve cells |
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catalase
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breakdown of hydrogen peroxide in peroxisomes
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adrenoleukodystrophy
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impaired beta oxidation of fatty acids - accumulation of long fatty acids in the brain and adrenal cortex
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Zellweger's Syndrome
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inability to import proteins into peroxisomes
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kearns-sayre syndrome
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affects eye movement due to abnormalities in mitochondrial DNA
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apoptosis
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opening of mitochondria via channel made of Bax Bak proteins, releasing cytochrome c into cytosol ==> proteolytic destruction of cell
positively regulated by BH3, negatively by Bcl2 |
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things that are imported into the nucleus
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lamins, histones, dna and rna polymerases, transcription factors, ribosomal proteins
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things that are exported from the nucleus
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tRNAs, mRNAs, ribosomal particles
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importin beta
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receptor for nuclear cargo (contains nuclear localization or export signals) aided by RAN GTPase that is involved in NPC control mechanism
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acrocentric chromosome
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contains satellit attached to stalk
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submetacentric chromosome
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short arms = p
long arms = q |
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metacentric chromosome
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arms are all the same length
centromere = primary constriction |
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Down syndrome
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trisomy 21
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Klinefelter's syndrome
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XXY male
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ionophore
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punches holes in nuclear membrane - influx of calcium
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G1 phase
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one centromere consisting of 2 centrioles (mother and daughter) surrounds by pericentriolar material
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G1 --> S phase
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centrosomes duplicate (transition is controlled by restriction point) - absence of signaling molecules forces cell to enter resting G0 phase
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leptotene
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phase of prophase when synaptonemal complex assembles - condensation of chromosome into visible strands
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zygotene
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phase of prophase where homologs synapse
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pachytene
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phase of prophase where crossing over occurs - looks like one really dense chromosome
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diplotene
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phase of prophase where the synaptonemal complex degrades
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spermatogonium
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in Mitosis - near basal lamina of seminiferous tubule
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spermatocyte
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in Meiosis I - primary --> secondary transition
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spermatid --> spermatozoon transition
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occurs during Meiosis II - enter lumen of seminiferous tubule
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acrosomal reaction
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The membrane surrounding the acrosome fuses with the oocyte membrane, exposing antigens and enzymes of the acrosome needed to break through touggh coating to allow fertilization to occur - after fertilization there is an influx of calcium that creates a barrier to block penetration by other sperm
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4 basic types of tissue
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epithelial, connective - classified by morphology
muscular, nervous - classified by function |
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fun facts about epithelium
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-can come from any of the 3 embryonic layers -whichever the organ system they belong to comes from
-classified by shape and number of layers -functions include protection, absorption, secretion -avascular, so they are located near blood supply in CT -produces basal lamina -contains apical, lateral and basal domains -stains darker than CT |
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derivation of glands
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come from epithelial downgrowth
exocrine maintain a duct to remain in contact with the exterior endocrine are surrounded by capillaries and produce hormones that are released into the blood or locally to the CT |
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mucous glands
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glycosylated proteins secreted in water soluble granules - stain lightly - flattened nuclei
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serous glands
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proteins are not glycosylated, less soluble so the granules remain intact - stain darker - round nuclei
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basement membrane
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site of interaction between epithelium and CT
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structure of cilia
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motile - 9 + 2 arrangement of microtubule doublets - dynein and nexin connections
primary - 9 + 0 configuration basal foot - coordinates movement alar sheet - attaches cilia to plasma membrane - gives stability striated rootlet - anchors cilium to cell |
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nodal cilia
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found in embryo, play role in organ positioning
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basal lamina structure
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type IV collagen, laminin, integrin (transmembrane), nidogen, perlecan
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mucosa
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epithelium + CT lining hollow organs
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serosa
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thin outer layer of simple squamos cells and underlying CT
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