Cellular Flashcards
p53 and hypophosphorylated Rb
Normally inhibit G1 to S progression
Permanent Cells
Remain in G0, regenerate from stem cells
Neurons, skeletal, cardiac and RBCs
Stable (quiescent) Cells
Enter G1 from G0 when stimulated
hepatocytes and lymphocytes
Labile Cells
Never go to G0. Divide rapidly with a short G1. Most affected by chemo
BM, Gut epithelium, skin, hair follicles, germ cells
Nissl bodies
rER in neurons, synthesize peptide NTs
Free Ribosomes
unattached to any membrane, site of synthesis of cytosolic and organellar proteins
Site of syn of secretory proteins and of N-linked oligosaccharide addition to many proteins
rER
in mucus secreting goblet cells and small inestine and plasma cells
site of steroid synthesis and detoxification of drugs and poisons
sER
found in liver hepatocytes and steroid-producing cells of adrenals and gonads
Golgi modification
N-oligosaccharides on asparagine
O-oligosaccharides on serine and threonine
mannose-6-phos to proteins on way to lysosomes
I cell disease
inclusion cell disease. inherited lysosomal storage disorder
defect in phosphotransferase thus decrease mannose-6-phosphate and proteins are delivered extracellularly instead of to lysosome
coarse facial features, clouded corneas, restricted joint movement, and high plasma levels of lysosomal enzymes.
I cell disease. often fatal in childhood
Signal recognition particle (SRP)
ribonucleoprotein, traffic protein from ribosome to rER.
COPI
retrograde movement of proteins from golgi to golgi or golgi to ER
COPII
anterograde Golgi to golgi or ER to Golgi
Clathrin
trans-Golgi to lysosomes
plasma membrane to endosomes for receptor mediated endocytosis (LDL-R activity)
Organelle to catabolize very-long-chain-FAs, branched chain FA and AA
peroxisome
Proteasome
Barrel-shaped protein complex that degrades damaged of ubiquitin-tagged proteins
defects are implicated in Parkinson
Dynein
retrograde to microtubule + to (-)