MCM_Final_TBL7 Flashcards
(83 cards)
Extra Cellular Matrix is compised of…

- polysaccharide bound proteins
- spingolipids
- keep cell hydrated and protected

protruding structures
- connect cells together or
- serve specialized functions
- ex) villi
what lines the membrane?
- receptors
- other protein
- lipid rafts
- (help to illict the function of pumps)
where is the basement layer?
- located bellow the extra cellular matrix

which cystolic organelles are on the nucleus side of cell?
- rough ER
- mitochondria
- free ribosomes
which cystolic organelles are on the cell memebrane side of the cell?
- smooth ER
- peroxisomes
- golgi
- lysosomes
protein secretion
what is the path of an endogenous protein?
- transcription and translation –> ER –> golgi –> destination
plasma membrane and secretions
(ex of some cellular secretions…)
- salivatory gland secretes …
- mucosal gland secretes …
- pancreas secretes …
- nerve neuron secretes …
- saliva via liquid
- mucus via liquid
- digestive zymogens via secretory glands
- neurotransmitters via vesicles
endoplasmic recticulum
- two types
- made up of interconnect flat sacs called cisternae
- pathway: gene –> mRNA –> peptide
Rough ER
- studded on exterior
- functions:
- starts the synthesis of exported proteins
- makes proteins for other organelles (i.e lysomome proteins)
Smooth ER
- smooth and near… generally closer to the membrane side of cell bc of its r_ole in metabolic functions_
- Functions:
- stores G6P: sugar fate (decides if glucose leaves of stays in the cell)
- steroid hormone: estrogen
- detoxification: liver enzymes
- plasma membrane maintenance
Golgi
- functions: protein modification and sorting
takes proteins from ER:
- sorts proteins by destination
- can add futher chemical modifications (O-glycan, start N-glycan)
- barcode (ex is M-6-P)
- packages into vesicles for transport
- membrane LIPID maintenance
Transport Proteins: COPII goes …
from ER to Golgi (anterograde/forward)
Transport Proteins: Clatherin…
- forms later vesicles for export (anterograde/forward)
Transport Proteins: COPI goes…
Golgi to ER (retrograde/backwards)
__________ + __________ transport proteins initiatie the process of ____________ of vesicles
Two pathways are (1) (2)
- COPII + Clathrin transport proteins initiatie the process of exocytosis of vesicles
-
constitutive secretory pathway (released immediately and is default of cells)
- ex) pancreas —> digestive emzymes
- lymphocytes
-
regulated secretory pathway (stored in vesicles and needs a signal to bind to receptor before it secretes)
- ex) neuron —> neurotransmitter
- insulin, histamine, hormones

endocytosis
- takes into the cell and the mechanism is DEPENDENT ON SIZE
- immune cells use phagocytsis (repsonse)
- duodenum cells use transporters (carb intake)
mitochondria
- double membrane organelle, essential for metabolism
- contains its OWN small circular DNA
Functions:
- ATP production via TCA, Oxidative Phosphorilation (ETC), B-Oxidation
- cell fate: apoptosis
Lysosomes
- cell DIGESTION and RECYCLING
- low pH to DENATURE biomolecules
- contains many HYDROLASE enzymes that function at low pH
- IMPERMEABLE membrane to enzymes
- made from GOLGI
- can FUSE with organelles and plasma membrane
Functions of Lysosomes (1-4)
- RECYCLES biomolecules to generate monomers or units for export
- AUTOPHAGY: organelle recycling through fusion (lysosome will fuse with mitochondria to for cell to make new mitochondria)
- MOVE LIPIDS between plasma membrane and golgi via FUSION
- G-6-P STORED HERE (glycolysis)
peroxisomes
- involved in oxidative digestion and from ER
Functions: contian oxidative enzymes
- B-oxidation of VERY LONG FA
- A-oxidation of BRANCHED CHAIN AA
- AA oxidase
- oxidative SYNTHESIS of BILE & CHOLESTEROLE
- has to catalase to eliminate H2O2
Zellweger Spectrum Disorders
- errors** in the **formation of peroxisomes with different severity due to PEX genes

Zellweger Syndrome
- MOST SEVERE
- very low peroxisome formation

Infant Refsum Disease
- due to lack of peroxisomes/beta-oxidation of VLCFA, the very long chain FA accumulate
- leads to:
- cranial abnormalities
- seziures
- vison/hearing loss



































