Anatomy and Physiology > Ch3 Cellular Form and Function > Flashcards

Ch3 Cellular Form and Function Flashcards

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1
Q

Cells shapes and sizes ___

A

Cells shapes and sizes VARIES

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2
Q

Most human cell sizes are ___ µm (micrometer) in diameter.

A

Most human cell sizes are 10-15 µm (micrometer) in diameter.

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3
Q

Egg cells (very large) are ___ in diameter

A

Egg cells (very large) are 100 µm in diameter

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4
Q

Muscle cells can be ___ cm long

A

Muscle cells can be 30 cm long

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5
Q

Nerve cells can be ___ meter(s) long

A

Nerve cells can be 1 meter long

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6
Q

Cell growth ____ volume more than surface area

A

Cell growth INCREASES volume more than surface area

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7
Q

Plasma (cell) membrane is _____ ______, surrounds ____ and ______ entry/exit - on perimeter of the cell

A

Plasma (cell) membrane is SELECTIVELY PERMEABLE, surrounds CELL, and REGULATES entry/exit - on perimeter of the cell

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8
Q

The cytoplasm is the ___ ____ of the cells

A

The cytoplasm is the INNER CONTENTS of the cells

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9
Q

What are the 3 things located in the cytoplasm?

A
  1. Organelles
  2. Cytoskeleton
  3. Cytosol (intracellular fluid, ICF)
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10
Q

98% of molecules in plasma membrane are ____.
The other 2% are ____.

A

98% of molecules in plasma membrane are LIPIDS (mostly phospholipids).
The other 2% are PROTEINS.

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11
Q

What 3 things can phospholipids be?

A
  1. Amphiphilic
  2. Hydrophilic
  3. Hydrophobic
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12
Q

How are amphiphilic molecules arranged?

A

In bilayer

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13
Q

What way do hydrophilic phosphate heads face?

A

Towards the water

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14
Q

Where are hydrophobic tails directed towards?

A

Towards the center

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15
Q

What way do phospholipids drift from place to place?

A

Laterally

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16
Q

What keeps membrane fluid in phospholipids?

A

Movement

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17
Q

What 2 other lipids are molecules in the plasma membrane?

A
  1. Cholesterol
  2. Glycolipids
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18
Q

What are glycolipids?

A

1/2 sugar and 1/2 lipids - contribute to glycocalyx

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19
Q

What are the 2 membrane proteins?

A
  1. Transmembrane proteins
  2. Peripheral proteins
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20
Q

What are transmembrane proteins?

A

Proteins that cross over from one side to other side in membrane (go from ECF to ICF).

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21
Q

What are peripheral proteins?

A

Proteins that are between the plasma membrane and the ICF.

  • adhere to face of membrane
  • usually tethered to cytoskeleton
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22
Q

What are the functions of the membrane protein?

A
  1. Receptors - receives and binds to something (hormone, neurotransmitter, etc)
  2. Second messenger systems - receptors & enzymes working together - signaling for a change to occur inside the cells
  3. Enzyme - breaks things down
  4. Ions channels

(Channel protein - gate constantly open and allows solutes to pass into and out of cell & gated channel - gate that opens and closes to allow solutes through only at a certain time, something has to happen to let it through)

  1. Carriers - transmembrane proteins that bind to glucose, electrolytes, and other solutes & transfer them to other side of membrane (some carriers, called pumps, consume ATP in process)
  2. Cell - identity marker - identifies cell for who it is (distinguishes body’s own cells from foreign cells, example: kidney donation line up closely to receiver?)
  3. Cell-adhesion molecule (CAM) - help link cells together
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23
Q

What are second messenger systems?

A

Receptors and enzymes working together in a way that they create a second messenger system and it’s a way of signaling for a change to occur inside the cell

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24
Q

What are glycocalyx?

A

Unique fuzzy coat external to plasma membrane

  • carbohydrate moieties of membrane glycoproteins and glycolipids
  • unique (except identical twins)
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25
What are the functions of glycocalyx?
1. Protections 2. Immunity/defense 3. Transplant compatibility 4. Cell adhesion 5. Embryonic development 6. Fertilization
26
What are membrane extensions?
Microvilli - numerous and small (1-2 µm) - increases cell’s surface area
27
What do microvilli specialize in?
Cells specialized in absorption
28
What are microvilli called when they are very dense?
“Brush border”
29
What are cilia? How long are they?
Hairlike processes 7-10 µm long
30
Where are motile cilia located?
In respiratory tract, uterine tubes, brain’s ventricles, efferent ductules of testes - beat in waves, sweep substances - power strokes, recovery strokes
31
What is axoneme?
The core of cilia - structural basis for cilary movement
32
What are microtubules?
“Tent poles” of cilia
33
What is the structure of microtubules?
9+2
34
What do microtubules form inside the cell?
Form basal body inside the cell
35
What do dynein arms do?
They “crawl” up adjacent microtubules, bending cilia
36
What is a flagella and what is it’s structure?
Tail of sperm - only functional flagellum -whiplike structure with axoneme identical to cilium
37
What are pseudopods?
Extensions that change
38
The plasma membrane is...
Selectively permeable - controls which things enter/leave cells
39
Does passive transport require ATP?
No.
40
What are the types of passive transport?
1. Filtration 2. Simple diffusion 3A. Carrier-mediated facilitated diffusion
41
Does active transport require ATP?
Yes
42
What are the types of active transport?
3B. Carrier-mediated (active) transport 4. Vesicular transport
43
What is filtration?
Particles driven through a selectively permeable membrane by hydrostatic pressure ex) filtration through capillary walls
44
What is simple diffusion?
Net movement of particles from HIGH to LOW concentration - due to constant, spontaneous motion - movement "down the concentration gradient"
45
What factors affect diffusion rate through membrane?
1. Temperature: high temp, high motion of particles 2. Molecular weight: larger molecules move slower 3. Steepness of concentrated gradient: high difference, high rate 4. Membrane surface area: high area, high rate 5. Membrane permeability: high permeability, high rate
46
Diffusion through lipid bilayer
Smaller & nonpolar most easily Ex) O2, CO2, & NO
47
Diffusion through channel proteins
Larger & more polar molecules Ex) glucose, ions
48
Cells control permeability by...
Regulating number of channel proteins or by opening and closing gates
49
What is osmosis?
Flow of water through selectively permeable membrane -from side with more water to side with less water
50
What are aquaporins?
Channel proteins that can increase rate of osmosis
51
What is osmotic pressure?
Amount of hydrostatic pressure required to stop osmosis -reverse osmosis
52
What is tonicity?
The ability of a solution to affect the fluid volume and pressure in a cell
53
Describe hypotonic solution
- lower concentration of nonpermeating solutes - thus higher water concentration - cells in this solution absorb water (even lyse!)
54
Describe hypertonic solution?
- has higher concentration of nonpermeating solutes - thus lower water concentration - cells in this solution lose water & shrivel
55
What are isotonic solutions?
Concentrations in cell = ICF
56
What is carrier-mediated transport?
Proteins that carry solutes across cell membrane
57
What are the carriers of of carrier-mediated transport?
* Uniport - 1 solute at a time * Symport - 2 solutes simultaneously, same direction * Antiport - 2 solutes simultanously, opposite direction
58
Solute binds to a ___ \_\_\_\_ on carrier protein
Solute binds to a RECEPTOR SITE on carrier protein
59
What are the types of carrier-mediated transport?
1. Facilitated diffusion 2. Active transport
60
What is facilitated diffusion?
- Solute through a membrane down its concentration gradient - no ATP consumed
61
What is active transport?
- Carrier-mediated transport of solution through membrane up (against) it's concentration gradient - uses ATP
62
What is vesicular transport?
- Transport of large particles or fluid droplets through membrane in vesicles or membrane - uses ATP
63
What is exocytosis?
Vesicular transport out of cell
64
What is endocytosis?
Vesicular transport into the cells
65
What are the 3 types of endocytosis?
1. Phagocytosis 2. Pinocytosis 3. Receptor-mediated endocytosis
66
Describe phagocytosis, pinocytosis, and receptor-mediated endocytosis.
1. Phagocytosis - engulfing large particles (eg. pathogens) 2. Pinocytosis - taking in fluid droplets 3. Receptor-mediated endocytosis - taking in specific molecules
67
What does exocytosis do?
- Secretes material (cells get rid of waste) - Replaces membrane removed by endocytosis
68
What is the cell interior?
Cytoplasm
69
What are the structures in the cytoplasm?
1. Cytoskeleton 2. Organelles 3. Inclusions \*\* all embedded in a clear gelatinous cytosol
70
What is a cytoskeleton?
Protein filaments and tubules (in the cytoplasm of living cells) that helps maintain shape and internal organization
71
What is the cytoskeleton composed of?
1. Microfilaments - of protein actin 2. Intermediate filaments 3. Microtubules - of protein tubulin
72
Describe microfilaments
Microfilaments - of protein actin - supports membrane & microvilli - produces cell movement
73
Describe intermediate filaments
Tight junctions
74
Describe microtubules
Microtubules - of protein tubulin - hold organelles in place, maintain cell shape - inside cilia, flagellum - move cargo
75
Be able to locate things in this picture
76
Describe a nucleus
- Largest organelle - usually one, few cells anuclear or multinucleate
77
Describe nuclear envelope
Membranes that surround nucleus; nuclear pores
78
Define nucleolus
Ribosome synthesis (reponsible for making ribosomes)
79
What does the endoplasmic reticulum (ER) consist of?
Rough ER & Smooth ER
80
Describe Rough ER
Cisternae (system of tunnels interconnected) covered with ribosomes - continuous with outer membrane of nuclear envelope - function: protein synthesis
81
Describe smooth ER
Smooth because no ribosomes in it - cisternae seem continuous with rough ER - function: steroids (+ other lipids) synthesis detoxifies alcohol, drugs
82
Define ribosomes
Small granules of protein & RNA -"read" coded genetic messages (messenger RNA), assemble amino acids into proteins
83
Describe golgi complex
System of cisternae; function: synthesize carbohydrates and modify proteins - receives newly synthesized proteins from rough ER - packages proteins into membrane-bound golgi vesicles * some become lysosomes * some become secretory vesicles
84
Describe lysosomes
Catabolic enzyme bound in membrane "cleaner uppers" Functions: * intracellular hydrolytic digestion * autophagy - digestion of worn out organelles * autolysis - "cell suicide" = programmed cell death * (glucose mobilization - in liver cells, lysosomes break down glycogen)
85
Describe peroxisomes
Resemble lysosomes but use different enzymes - use O2 to oxidize organic molecules - neutralize free radicals, detoxify alcohol - break down fatty acids into acetyl groups for midochondrial use (ATP synthesis) - hydrogen peroxide (H2O2) produced buy catalase breaks that down - in all cells but abundant in liver and kidney
86
What are proteasomes?
Protein disposal
87
Describe mitochondria
Synthesizes ATP -double unit membrane * inter folds= cristae (enzymes necessary to produce ATP) * matrix contains ribosomes, enzymes for ATP synthesis, and small circular DNA molecule = mitochondrial DNA - "powerhouses" * energy extracted from organic molecules (glucose), transferred to ATP
88
Describe centrioles
- composed of microtubules - organizes chromosomes during cell division - form basal body of cilium or flagellum
89
What are inclusions?
Stored cellular products -disease markings
90
Why should we care about Zellweger syndrome?
Hereditary genetic disorder that affect peroxisomes (organelles found in almost all body cells). It disturbs cellular function and causes serious problems soon after birth. Newborns can have brain, liver and kidney problems, as well as difficulty feeding or moving. There is no cure or treatment. Peroxisomes are responsible for many important cell processes, including energy metabolism, which means that Zellweger syndrome can severely impact the body
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