Cell Organelles Flashcards
What organelle makes up the largest percentage of total cell membrane volume in a liver hepatocyte and in a pancreatic exocrine cell
Liver hepatocyte- Mitochondria
Pancreatic exocrine cell- Rough ER
Functions of smooth ER, and what type of cell would have a large amount of smooth ER
Glycogen metabolism Lipid/phospholipid synthesis Detoxification Steroidgenesis Calcium regulation -Abundant in cells that make steroids or lipids
Cis vs Trans colgi
Cis is usually the entrance point of proteins coming from rough ER. Trans is usually the exit point
Golgi functions
Modifications of carbs attached to glycoproteins
Poly/oligosaccharide synthesis
Synthesis of sphingomyelin
Sorting secretory products, packaging into vesicles
Clathrin coated vesicles are used for
Transporting products from Golgi to lysosomes or from exterior of cell to lysosomes
COPI coated vesicles are used for
Transporting products b/w stacks of the Golgi apparatus
COPII coated vesicles are used from
Transporting products from ER to the golgi
What is Dynamins function
Surrounds neck of the invaginated clathrin coated pit, causing neck of the vesicle to pinch off from plasma membrane
What is Adaptins function
Mediates clathrin binding to the vesicle membrane
How are lysosomal enzymes sorted
In the Golgi, they get a Mannose-6-phosphate attached to them, which attaches to the M6P receptor in the trans Golgi where it buds off as a clathrin coated vesicle and eventually loses the clathrin and becomes a lysosome
Difference b/w primary and secondary lysosomes
Primary lysosomes are storage site for hydrases, no enzymatic activity. Secondary lysosomes are engaged in catalytic processes and have active enzymes
Characteristics/cause of familial hypercholesterolemia
Characterized by elevated levels of LDL (the primary transport protein for cholesterol)
Primary defect is mutation in the gene encoding the LDL receptor
-leads to atherosclerotic plaques
Peroxisome functions
Synthesis/degradation of hydrogen peroxide
B-oxidation of LCFA
Bile acid/cholesterol synthesis
Detoxify alcohol
Zellwinger syndrome
Absence of or reduced numbers of peroxisomes
Caused by defects in the assembly of the peroxisome
What is a major cause of mitochondrial DNA diseases
Mutations in mt tRNA genes