cellular + a sprinkle of lab techniques Flashcards

(48 cards)

1
Q

CDKs?

A

cell cycle regulators

constitutive and inactive

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2
Q

cyclins?

A

cell cycle regulators

phase specific, activate CDKs - form complexes

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3
Q

cyclin-CDK complexes?

A

phosphorylate proteins –> cell cycle progression/coordination

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4
Q

tumor suppressor function?

A

p53, Rb - prevent progression from G1 to S

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5
Q

which cells are “permanent” (remain in G0)?

A

neurons, mm, RBCs - regenerate from stem cells

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6
Q

which cells are “stable/quiescent” (enter G1 when stimulated)?

A

hepatocytes

lymphocytes

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7
Q

which cells are “labile” (no G0, divide rapidly)?

A

bone marrow, gut epithelium, skin, hair follicles, germ cells

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8
Q

what happens in the RER?

A

synthesis of proteins and post-translational modification

free ribosomes –> cystosolic and organellar proteins

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9
Q

what’s a Nissl body?

A

RER of neurons - makes peptide neurotransmitters

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10
Q

which types of cells have a sh*t-ton of RER?

A

mucus-secreting goblet cells in SI

Ab-secreting plasma cells

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11
Q

what happens in the SER?

A

steroid synthesis
detox (CYP450)

No surface ribosomes

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12
Q

which types of cells have a sh*t-ton of SER?

A

liver hepatocytes

steroid-hormone producing cells (adrenal cortex and gonads)

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13
Q

what happens in the nucleolus?

A

rRNA transcription

processing of ribosome assembly

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14
Q

what happens in the Golgi?

A

protein/lipid distribution
asparagine N-oligosaccharide modification
ser/thr O-oligosaccharide addition
mannose-6-P added to proteins –> lysosome trafficking

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15
Q

what’s an endosome?

A

sorts material from outside cell or from Golgi

sends to lysosomes, membrane, or Golgi

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16
Q

coarse facial features, clouded corneas, restricted joint movement, high plasma levels of lysosomal enzymes?

A

inclusion cell disease
defect in N-acetylglucosaminyl-1-phosphotransferase
Golgi can’t add mannose6P to protein –> extracellular instead of lysosomal secretion

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17
Q

what is a signal recognition particle?

A

cytosolic ribonucleoprotein
traffics proteins from ribosome to RER

** if absent: accumulation of proteins in cytosol

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18
Q

what does COPI do?

A

mediates retrograde trafficking in Golgi and from cis-Golgi to ER

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19
Q

what does COPII do?

A

mediates anterograde trafficking from ER to cis-Golgi

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20
Q

what does clathrin do?

A

mediates:
trans-Golgi –> lysosomes
plasma membrane –> endosomes

21
Q

what happens in the peroxisome?

A

catabolism of VLCFAs, branched chain FAs, AAs

22
Q

what happens in the proteasome?

A

degradation of damaged or ubiquitinated proteins

** defects implicated in Parkinson’s

23
Q

what do microfilaments do?

A

muscle contraction

cytokinesis

24
Q

what do intermediate filaments do?

A

maintain cell structure

25
what do microtubules do?
movement | cell division
26
what does vimentin stain for?
connective tissue?
27
what does desmin stain for?
muscle (desMin)
28
what does cytokeratin stain for?
epithelial cells
29
what does GFAP stain for?
neuroglia
30
what is the structure of a microtubule?
alpha and beta tubulin heterodimers with 2 GTP bound dynein: retrograde transport kinesin: anterograde transport
31
which drugs act on microtubules?
``` Microtubules Get Constructed Very Poorly: mebendazole griseofulvin colchicine vincristine/vinblastine paclitaxel ```
32
what is the structure of cilia?
9+2 microtubulae doublet arrangement | axonemal dynein
33
what does ouabain do?
binds K+ site on Na-K ATPase
34
how does dig work?
direct inhib of Na-K ATPase --> indirect inhib of Na/Ca exchange --> increased Ca --> increased cardiac contractility
35
where are the types of collagen found?
``` Be (So Totally) Cool, Read (Better) Books! type I: bone, skin, tendon type II: cartilage type III: reticulin, blood vessels typve IV: basement membrane, lens ```
36
which dz involves type I collagen?
OI
37
which dz involves type III collagen?
vascular type Ehlers Danlos
38
which dz involves type IV collagen?
Alport | Goodpasture
39
what are the steps of collagen synthesis?
1) synthesis in the RER: translation of preprocollagen (gly-pro-lys) 2) hydroxylation in RER: pro and lys, needs vit C 3) glycosylation in RER: hydroxylysine glycos, hydrogen and disulfide bond formation --> procollagen 4) exocytosis 5) proteolytic processing: cleavage of disulfide terminals --> tropocollagen 6) crosslinking: lys-hydroxylys (lysyl oxidase needs Cu) --> fibrils
40
multiple fractures with minimal trauma, blue sclerae, hearing loss, dental imperfections?
OI - AD | decreased prod of otherwise normal type I collagen (problems forming procollagen)
41
hyperextensible skin, easy bleeding, hypermobile joints, berry aneurysms, aortic aneurysms?
Ehlers Danlos - many inheritance types type V: classic, jt and skin type III: vascular and organ rupture
42
brittle kinky hair, growth retardation, hypotonia?
Menkes - XLR defect in ATP7A --> defective Cu transport/absorption decreased activity of lysyl oxidase --> decreased collagen synthesis
43
what is the structure of elastin?
nonhydroxylated proline, glycine, lysine tropoelastin + fibrillin scaffolding broken down by elastase (a1at inhibits elastase)
44
where is elastin found?
``` skin lungs large aa ligaments vocal cords ligamentum flavum ```
45
steps of PCR?
denaturation annealing elongation
46
what's with all the f***ing blots?
SNoW DRoP: southern = DNA Northern = RNA Western = protein (sneaky sneaky: southwestern = DNA-binding proteins!) if we have to know any more than that, fuck it
47
direct vs indirect ELISA?
direct: test Ab looks for specific antigen indirect: test Ab/Ag looks for specific Ab-Ag complex
48
cre-lox system?
inducibly manipulates genes at specific developmental points