Cell Organelles Flashcards

1
Q

What organelle makes up the largest percentage of total cell membrane volume in a liver hepatocyte and in a pancreatic exocrine cell

A

Liver hepatocyte- Mitochondria

Pancreatic exocrine cell- Rough ER

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2
Q

Functions of smooth ER, and what type of cell would have a large amount of smooth ER

A
Glycogen metabolism
Lipid/phospholipid synthesis
Detoxification
Steroidgenesis
Calcium regulation
-Abundant in cells that make steroids or lipids
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3
Q

Cis vs Trans colgi

A

Cis is usually the entrance point of proteins coming from rough ER. Trans is usually the exit point

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4
Q

Golgi functions

A

Modifications of carbs attached to glycoproteins
Poly/oligosaccharide synthesis
Synthesis of sphingomyelin
Sorting secretory products, packaging into vesicles

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5
Q

Clathrin coated vesicles are used for

A

Transporting products from Golgi to lysosomes or from exterior of cell to lysosomes

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6
Q

COPI coated vesicles are used for

A

Transporting products b/w stacks of the Golgi apparatus

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7
Q

COPII coated vesicles are used from

A

Transporting products from ER to the golgi

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8
Q

What is Dynamins function

A

Surrounds neck of the invaginated clathrin coated pit, causing neck of the vesicle to pinch off from plasma membrane

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9
Q

What is Adaptins function

A

Mediates clathrin binding to the vesicle membrane

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10
Q

How are lysosomal enzymes sorted

A

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

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11
Q

Difference b/w primary and secondary lysosomes

A

Primary lysosomes are storage site for hydrases, no enzymatic activity. Secondary lysosomes are engaged in catalytic processes and have active enzymes

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12
Q

Characteristics/cause of familial hypercholesterolemia

A

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

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13
Q

Peroxisome functions

A

Synthesis/degradation of hydrogen peroxide
B-oxidation of LCFA
Bile acid/cholesterol synthesis
Detoxify alcohol

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14
Q

Zellwinger syndrome

A

Absence of or reduced numbers of peroxisomes

Caused by defects in the assembly of the peroxisome

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15
Q

What is a major cause of mitochondrial DNA diseases

A

Mutations in mt tRNA genes

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