Cells 1 Flashcards

(46 cards)

1
Q

What does the fluid mosaic model display?

A

lipid bilayer

integral/peripheral proteins

glycoproteins

transport across membrane

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2
Q

what is endocytosis?

A

taking up material from the outside and bringing it inside the cell

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3
Q

what are the 3 types of endocytosis?

A

1) phagocytosis
2) pinocytosis
3) receptor mediated endocytosis

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4
Q

what is phagocytosis?

A

take up of solid material from the outside to inside

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5
Q

what is pinocytosis?

A

take up of water form the outside

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6
Q

what is receptor mediated endocytosis?

A

taking up specific material

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7
Q

What is the structure of the mitochondria?

A

outer membrane

intermembrane space

inner membrane

cristae

matrix

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8
Q

what is the function of the mitochondria?

how do they stain?

A

powerhouse of the cell (ATP)

stain red, eosinophillic

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9
Q

what is this?

A

mitochondria

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10
Q

Mitochondrial diseases cause what mainly?

what is the primary target of mitochondrial diseases?

A

a decrase in production of ATP, increase in lactic acid

heart and brain

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11
Q

what is the structure of the RER?

what is the function of RER?

A

folds studded with ribosomes

they help with glycosylation of proteins

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12
Q

what is the structure of the SER?

what is the function of SER?

A

smooth folds

they help with detox and lipid synthesis, metabolism of carbohydrates

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13
Q

what type of microscopy is this?

A

TEM

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14
Q

how is the RNA in ribosomes stained?

A

basophilic

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15
Q

what is the esosinophilic structure here?

A

mitochondria

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16
Q

What is the function of the golgi complex?

A

packaging and transport (redistribution) to other parts of cell

Also helps with exocytosis

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17
Q

what do lysosomes do?

A

they are in charge of degradation by enzymes

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18
Q

what organelle is this?

A

lysosomes

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19
Q

what is lipofuscin?

A

when material cant be degraded by lysosome and stays a while

20
Q

what organelle is this?

21
Q

What is a proteosome?

A

degrade damaged or unneeded proteins by tagging them with ubiquitin

22
Q

What are 3 ubiquitin proteosome disorders?

A

astrocytomas

parkinson’s (lewy bodies)

alzheimers (amyloid)

23
Q

What is the structure indicated by the arrow?

24
Q

What do peroxisomes do?

A

they break down very long fatty acid chains

they make myelin

25
What is this structure?
peroxisomes
26
What are the main 3 components of the cytoskeleton?
1) microfilaments 2) intermediate filaments 3) microtubules
27
What are microfilaments made of?
actin dimers
28
what do microtubules do?
hollow tubes that move organelles, vesicles and ribosomes
29
What are microtubules made off?
alpha and beta tubulin dimers that form protofilaments (alpha is - end; beta is + end)
30
towards what end is there elongation in a microtubule?
towards the postitive since the negative end is capped
31
What are the molecular motors?
kinesin (form - to +; to periphery) dyenin (from + to negative; from periphery to cell)
32
What structure contains a 9+2 conformation?
cilia
33
how are microtubules in centrioles organized?
nine triplets
34
What is actin?
are thin filaments of globular or filamentous protein than anchor membrane proteins.
35
what do actin filaments aid in?
they stiffen microvilli, aiding in absorption
36
What are the 5 different intermediate filaments?
1. tonofilaments 2. vimentin 3. desmin 4. neurofilaments 5. glial filaments
37
Where do tonofilements come from?
from epithelium
38
where does vimentin come from?
mesenchymal cells
39
where does desmin come from?
from muscle cells
40
where do neurofilements come from?
neurons
41
where do glial filaments come from?
from glial cells
42
Give an example of where do we find tonofilaments?
keratinizing and non-keratinizing epithelia
43
Give an example of where we can find vimentin?
fibroblast, chondroblast, osteoblast, macrophages
44
give an example of where we can find desmin?
striated and smooth muscle
45
give an example of where we can find neurofilaments?
neurons
46
give an example of where we can find glial filaments?
astrocytes