Lecture 4, 6, 7 Flashcards

(50 cards)

1
Q

List and describe the structure & function of the nucleus

A

Structure: Largest organelle in the cell

  • 10% volume
  • DNA sequestered in nucleus

Function:

  • houses
    1. nucleolus- site of ribosome production
  • has 3 zones
    a: Fibrillar center - pale region of DNA loops of 5 chromosomes
    b: Fibrillar material- transcription of rRNA genes
    c: Granular material - initial ribosomal assembly
  1. nuclear envelope- inner and outer mem
  2. nuclear lamina- mesh like sheet
  3. nuclear pores
    - made up of >50 protein (nucleoporins)
    - allow transport of molecules btw nucleus
    and cytoplasm
    - ions 9 nm = active transport
  4. nucleoplasm
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2
Q

Ribosome

A

Structure:

  • made in nucleus
  • leaves nucleus and goes to cytoplasm
  • 2 ribosomal RNA subunits and associated proteins
  • has: membrane bound ribosomes + free ribosomes

Function:
- site of protein synthesis (translation)

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3
Q

Endoplasmic Reticulum

A

Structure: interconnected network that spans cytoplasm
- ER mem continuous with nuclear envelope membrane

Function:
- allows protein and lipids to travel from nucleus because it comes in contact with Nuclear Pore Complex

  • two regions:
    1. Smooth ER
    2. Rough ER
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4
Q

RER

A

Structure: has membrane bound ribosomes and structure is continuous with plasma membrane. The ribosome is where tRNA and mRNA come in to produce protein from mRNA.
- next to nucleolus which makes ribosomes

Function:
synthesis of proteins destined for plasma membrane, lysosomes, or secretion

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5
Q

SER

A

Structure: lacks ribosomes

Function:
- synthesis of lipids and detoxification

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6
Q

Golgi

A

Structure: flat membrane enclosed cistern

  • located next to nucleus + centrosome
  • microtubule dependent
  • esp well developed in secretory cells: rER -> sends golgi –> secretory
  • 2 faces:
    • CIS/ CGN (cis golgi network); entry
    • TRANS/ TGN (trans golgi network); exit

Function:

  • post translational modifications
  • processes, packages, transports synthesized protein from Golgi to lysosome via TGN

rER- Golgi - lysosomal pathway, constitutive secretory pathway, regulated secretory pathway

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7
Q

Lysosome

A

Structure:
membrane enclosed compartments with hydrolytic enzymes which need an acidic envt

Function:
digestive organelles

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8
Q

Peroxisome

A

Structure: small organelle
- made by free ribosomes (cytoplasmic) - sER

Function:

  • fat metabolism (B oxidation enzymes, FA oxidation, catalyze initial reactions in formation of plasmalogens
  • deficiencies cause: abnormalities in myelination of nerve cells because they normally have phospholipids in myelin
  • degrade toxic reactive oxygen molecules
  • have catalase
  • convert H202 to O2 and water
  • liver: detox of ingested alcohol
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9
Q

Mitochondria

A

Structure:

  • 2 membranes = outer and inner
  • 2 compartments = intermembrane space and matrix
Function: look at slide 64***
generate ATP via:
TCA
oxidative phosphorylation 
B oxidation of FA

Diseases:

  1. MERRF: myoclonic epilepsy with ragged red fibers
    - mutation in tRNA gene
  2. Leber hereditary optic neuropathy
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10
Q

Describe the structure and function of the nucleolus, nuclear envelope and nuclear
pore complex.

A

Nucleolus:

  • site of ribosome production
  • has 3 zones
    a: Fibrillar center - pale region of DNA loops of 5 chromosomes
    b: Fibrillar material- transcription of rRNA genes
    c: Granular material - initial ribosomal assembly

Nuclear Envelope:

  • inner membrane= functions as scaffold stabilizing the nuclear envelope
  • outer membrane= continuous with RER; contains ribosomes
Nuclear Pore Complex: 
 - made up of >50 protein (nucleoporins)
 - allow transport of molecules btw nucleus   
  and cytoplasm 
 - ions 9 nm = active transport
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11
Q

Describe the organization of chromatin structure.

A

Chromatin= is chromosomes in various degree of uncoiling

- packaged into nucleosomes (protein/ histones + DNA)

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12
Q

Distinguish euchromatin and heterochromatin in a nucleus

A

Chromatin can be:

  1. Euchromatin: lightly stained
    - less condense = more transcriptionally active
  2. Heterochromatin: densely staining
    - highly condensed chromatin = less transitionally active
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13
Q

Predict cellular activity based on the chromatin structure. Describe the bi-directional vesicle transport between the endoplasmic reticulum and Golgi apparatus

A

Cellular Activity of chromatin Structure:
- Euchromatic: more transcriptionally active/ less condense
- Heterochromatin: less transcriptionally active/ more condense
- chromosome has centromere: centric
heterochromatin that holds sister
chromatids together during interphase

Bi-directional vesicle transport btw ER and Golgi: slide 48

  1. COP1: Retrograde = CGN - rER
  2. COP2: Anterograge = rER- CGN
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14
Q

Describe protein trafficking for lysosomes, secretion, plasma membrane, nucleus,
mitochondria, cytosol and peroxisomes.

A
  1. Membrane bound ribosomes:
    - attached to cytoplasmic surface of ER/ RER
    - synthesis protein translocated into ER lumen
  • ribosome -> ER -> Golgi -> lysosome, secretion, plasma membrane
  1. Free ribosome: unattached
    ribsome -> nuclear protein, MT protein, cytosolic protein, peroxisomal protein
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15
Q

List and describe the three cellular pathways to lysosomal degradation.

A
  1. phagocytosis
  2. endocytosis
  3. autophagy - self eating
    - intracellular membrane surrounds organelle + cytoplasm –> autophagosome formed –> fuses with lysosome –> degraded, recycled and reused
    - used for cell aging, cell death or starvation
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16
Q

Describe the types of intracellular inclusions

A

Inclusions: cytoplasmic or nuclear structures formed from metabolic products of the cell

1: Pigments
a: lipofucsin
- brown gold
- non dividing cells “wear and tear”
b: hemosiderrin
- brown
- iron storage
- formed from hemoglobin (spleen)
c: melanin
- brown pigment

  1. Glycogen
    - storage of glucose
    - non membrane bound dense bodies
  2. Lipid
    - non membrane bound dense bodies
    - fat droplets; liquid at room temp
    - energy store
    - source of short carbon chains
    - lipidoses (lipid storage disease
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17
Q

List the three major types of protein filaments that form the cytoskeleton.

A
  1. Microtubules
  2. Intermediate filaments
  3. Microfilaments
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18
Q

Describe the structure, function and assembly of microtubules, intermediate filaments and microfilaments.

A
Microtubules: 
Structure -->
- non branching, rigid, hollow tubes
- polar - and + end
- a/b tubulin 
- 25 nm

–> Function:
- intracellular transport
- cell motility (cilia and flagella)
- mitotic spindle
- rigid intracellular skeleton - cell shape and polarity
- have MAP: microtubule associated proteins i.e.:Tau (stabilize axonal microtubules) –> linked to Alzheimer’s
Note:
9 microtubules –> centriole (basal body for cilia and flagella)–> centrosome

Intermediate filaments:
Structure:
- 6 classes: 
a: 1, 2keratins- all epithelial cells
b: vimentin, vimentin like- mesoderm 
c: neurofilaments- neurons
d: lamins- nucleus 
e: beaded filaments- eye lens
  • 8-12 nm
  • nonpolar
  • rope like filaments

Function:

  • stabilize cell structure (maintain position of nucleus and other organelles
  • resist shearing forces (connect with desmosomes and hemidesmosomes; extend across cytoplasm)
  • essential for integrity of cell to cell and cell-ECM junctions

Microfilaments:

  • aka actin filaments
  • 7 nm
  • actin: g and f (f needs ATP)
  • polarized structure ( + and - polar ends needed for movt)
  • can be as single, bundle or networks
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19
Q

Describe the structure and function of the centrosome.

A

9 microfilaments arrange together –> create the centriole (basal body needed for cilia and flagella –> make up the centrosome

Centrosome structure: slide 70

  • has pair of centrioles so they are perpendicular to each other
  • amorphous(ill defined) protein matrix
  • y tubulin =nucleation site for microtubules

Centrosome function:

  • organize microtubules
  • neg end: microtubules nucleated
  • pos end: microtubules point out to periphery
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20
Q

Describe the structure and function of the primary cilia, cilia and flagella.

A

Primary cilia:

  • microtubule, antennae like
  • sensory antennae: chemoreceptor, photoreceptor, or mechanoreceptor (polycystic kidney disease)
  • 9+0

Cilia:

  • microtubules base, hair like structure
  • motile: synchronous
  • 9+2
  • pair of dynein arms
  • anchored to cell via basal body

Flagella:

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21
Q

List and describe the molecular motor proteins associated with microfilaments and microtubules.

A
Microtubules: Dynein Family 
- move along microtubules from + to -***
- meaning moving from lysosome to MT
- 2 members:
a: cytoplasmic dynein 
b: axonemal dynein 
    - cilia + flagella (most caused by bending of the core- 
    axoneme)

Microtubules: Kinesin
- move from - to + (cell body to out in periphery)

Microfilaments: Myosin
Myosin 2: generates force for muscle contraction
- has polar head that binds and hydrolyzes ATP
Stages:
1. attachment
2. release- ATP binds; reduce affinity for actin
3. bending- ATP hydrolysis
4. power stroke
5. reattachment

22
Q

Describe role of the cytoskeleton in intracellular transport and cellular motility.

A

Intracellular transport:

  1. Cilia and Flagella - via Microtubule Dynein
  2. Myosin via Microfilaments/ actin

Cellular motility:

  1. Protrusion- actin dependent
    - actin polymerization (monomer to polymer) at + end extends lamellipodium
  2. Attachment
    - actin anchored to ECM via integrin proteins
  3. Contraction
    - bulk of cells and cytoplasm dragged forward
23
Q

List and describe the three components of whole cell motility across a substrate.

24
Q

List and describe the three types of membrane protrusion structures.

A
  1. Filopodia
    - finger like projections
    - actin filaments
  2. Lamellipodia
    - sheet like structures
  3. Pseudopodia
    - 3D projections
25
Describe actin polymerization in membrane protrusion and motility.
ARP: actin related protein is located in front of lamellipodia where actin nucleation (formation) is most active
26
Describe the role of the neutrophil in the acute inflammatory response
Chemotaxis: | move along tissue along gradient towards inflammation
27
Describe the process of neutrophil recruitment and migration.
1. rolling 2. activation 3. adhesion 4. transendthelial migration - diapedesis
28
List and describe the three types of membrane-bound vesicles (granules) found in neutrophils.
1. 2. 3.
29
Describe the process of autophagy.
a: intracellular mem surrounds the organelle and cytoplasm b: autophagosome formed - double membrane vacuole c: fusion of autophagosome with lysosome d: contents are degrades, recycles, and reused
30
List and describe the two general pathways of exocytosis.
1. | 2.
31
List the three major classes of membrane lipids.
1. phospholipids 2. cholesterol 3. glycolipids
32
List and describe the five major phospholipids in the plasma membrane.
1. phosphatidylserine- moves from inner to outer leaflet (apoptosis) 2. phosphatidulethanolamine 3. phosphatidylcholine 4. phosphatidylinositol 5. sphingomyelin Phospholipids: have two FA tails, glycerol backbone, phosphate, then X group
33
Describe the structure and function of cholesterol in the cell membrane.
- Polar head which attaches to phospholipid bilayer - Nonpolar hydrocarbon tail - intercalates between phospholipids - reduces membrane fluidity (varies in high and low temperature)
34
Describe the structure and function of glycolipids in the plasma membrane.
Glycolipids: slide 9 - Have FA chain, FA tail, bound to monosaccharide or oligosaccharide - Outer monolayer - Function: Lipid (non polar) allows to attach to lipid bilayer and sugar (polar) so soluble in aq solution around cell
35
Describe the six categories of integral membrane proteins.
1. pumps/ carriers/ transporters 2. channels 3. receptors 4. enzymes 5. structural protein 6. linkers
36
Describe the structure and function of the glycocalyx.
Glycocalyx: cell coat 1. glycolipid 2. glycoprotein 3. proteoglycans
37
Describe the structure and function of the glycocalyx.
Glycocalyx: cell coat 1. glycolipid 2. glycoprotein 3. proteoglycans - Carb rich zone on cell surface - establish microenvt at cell surface - protection - cell recognition - cell to cell interaction (lectins)
38
Explain the fluid mosaic model of membrane structure.
Polar/ Hydrophilic Head --> exterior and cytosol Nonpolar/ hydrophobic FA tails --> core Have the ability to move with in the plane of the membrane
39
List the two major types of vesicular transport.
1. endocytosis | 2. exocytosis
40
Describe the precise targeting of vesicles within the cell.
Rab GTPase interact with tethering proteins --> vesicle immobilized ``` Accurate targeting 1. Vesicle specific membrane protein v-snare 2. Target specific membrane protein t-snare ```
41
List and describe the three different mechanisms of endocytosis.
1. Receptor Mediated - selective - clathrin dependent - form basket like cage - clarthin coated pits - clarthrin interacts with cargo receptors via Adaptin - dynamin 2. Pinocytosis- cell drinking - non specific - constitutive but mostly endothelial - clathrin independent - no receptor protein 3. Phagocytosis- cell eating - can ingest non biological material - done by specialized phagocytes i.e.: macrophage and neutrophil - bind ot plasma mem receptor and extend pseudopods --> then fuse with lysosome
42
List and describe the two general pathways of exocytosis.
1. Regulated - stored in cytoplasm and released when needed - secretory cells - stimulus - Ca influx - fusion of secretory vesicles with plasma membrane 2. Constitutive - substance continuously secreted to plasma membrane
43
List and describe the four pathways for processing internalized ligand receptor complexes
1. receptor recycled, ligand degraded 2. receptor and ligand recycled 3. receptor and ligand degraded 4. receptor and ligand transcytosis
44
Explain the histologic basis of lysosomal storage diseases.
- mutations in genes that code lysosomal enzymes - have increased undigested products - disruption of normal cell function - cell death
45
Describe Tay-Sachs disease.
- deficient in HEXA (B hexosaminidase A, ALPHA subunit - have accumulation of GM2 gangliosides - result: death of neurons in brain and spinal cord
46
Describe diseases related to nonfunctional peroxisomes and Zellweger syndrome.
- Nonfunctional peroxisomes cause abnormal myelination of nerve cells ie: Zellweger syndrome
47
Describe Tay-Sachs disease.
- deficient in HEXA (B hexosaminidase A, ALPHA subunit - have accumulation of GM2 gangliosides - result: death of neurons in brain and spinal cord
48
Colchicine
Anticancer compound - prevents polymerization- binds to tubulin - mitotic spindle breaks down - apoptosis related compounds - vinca akaloids ie: vinblastin - vinscristine
49
Taxol
anticancer drug - stabilized and prevents microtubule assembly - bind tubulin within assembled microtubules - arrests cells in mitosis - apoptosis - cannot achieve metaphase spindle conformation
50
Taxol
Anticancer drug - stabilized and prevents microtubule assembly - bind tubulin within assembled microtubules - arrests cells in mitosis - apoptosis - cannot achieve metaphase spindle conformation