Endocytosis
5 pathways
macropinocytosis
occurs in thyroid cells as they take up thyroglobulin and dendritic cells
clathrin mediated endocytosis
occurs at clathrin coated pits, dynamin is required to pinch of the vesicle, can be mediated by receptors or not
cholesterol
taken up by clathrin mediated endocytosis in the form of LDL
coated pits
clathrin mediated endocytosis
atherosclerosis
occurs when there is a decrease or defect in the LDL receptor
(clathrin mediated endocytosis)
non coated mediated exocytosis
Shiga and Cholera toxins
phagocytosis
Secretion
exocytosis
bulk secretion
sectretion of cellular synthetic products like proteins, enzymes, hormones, and neurotransmitters
secretory vesicles
perform in exocytosis
formed by the golgi, fuse with plasma membrane
in charge of intracellular trafficking
2 pathways of exocytosis
constitutive
regulated
constitutive exocytosis
continous secretory processes, secretory product is not stored in secretory granules
regulative exocytosis
secretory product is stored in secretory vesicles until a signal causes the product to be secreted
porocytosis
involved with secretion
release of neurotransmitters
exosomes & vesicles
ribosomes
basophillic
involved in protein synthesis
occur as: indv granules, polyribosomes that can be free or attached
NOT found in mature erythrocytes
free polyribosomes
polysomes
mRNA + ribosomes
protein synthesis for use in the cell
hemoglobin, mitochondrial proteins, peroxisomal proteins
rough ER
membranous, basophillic
intracellular network of cisternae
continuous with outer membrane of nuclear envelope that is studded with ribosomes
polyribosomes involved with Co translational translocation
attached to rER, translocation of growing polypeptide chains
Post Translational Functions
ER stress
accumulation of unfolded misfolded proteins in the ER cisterna
Unfolded protein response
1- chaperone protein synthesis increases
2-decreased synthesis of proteins
3- misfolded proteins are exported from ER to cytosol and then get degraded by proteasomes
4- caspases are activated which leads to apoptosis
alpha antitrypsin deficiency
AAT- mutant protein aggregates in ER