Lecture 4, 6, 7 Flashcards

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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.

A

3.

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
Q

Describe actin polymerization in membrane protrusion and motility.

A

ARP: actin related protein is located in front of lamellipodia where actin nucleation (formation) is most active

26
Q

Describe the role of the neutrophil in the acute inflammatory response

A

Chemotaxis:

move along tissue along gradient towards inflammation

27
Q

Describe the process of neutrophil recruitment and migration.

A
  1. rolling
  2. activation
  3. adhesion
  4. transendthelial migration
    - diapedesis
28
Q

List and describe the three types of membrane-bound vesicles (granules) found in neutrophils.

A
  1. 3.
29
Q

Describe the process of autophagy.

A

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
Q

List and describe the two general pathways of exocytosis.

A

1.

2.

31
Q

List the three major classes of membrane lipids.

A
  1. phospholipids
  2. cholesterol
  3. glycolipids
32
Q

List and describe the five major phospholipids in the plasma membrane.

A
  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
Q

Describe the structure and function of cholesterol in the cell membrane.

A
  • Polar head which attaches to phospholipid bilayer
  • Nonpolar hydrocarbon tail
  • intercalates between phospholipids
  • reduces membrane fluidity (varies in high and low temperature)
34
Q

Describe the structure and function of glycolipids in the plasma membrane.

A

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
Q

Describe the six categories of integral membrane proteins.

A
  1. pumps/ carriers/ transporters
  2. channels
  3. receptors
  4. enzymes
  5. structural protein
  6. linkers
36
Q

Describe the structure and function of the glycocalyx.

A

Glycocalyx: cell coat

  1. glycolipid
  2. glycoprotein
  3. proteoglycans
37
Q

Describe the structure and function of the glycocalyx.

A

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
Q

Explain the fluid mosaic model of membrane structure.

A

Polar/ Hydrophilic Head –> exterior and cytosol

Nonpolar/ hydrophobic FA tails –> core

Have the ability to move with in the plane of the membrane

39
Q

List the two major types of vesicular transport.

A
  1. endocytosis

2. exocytosis

40
Q

Describe the precise targeting of vesicles within the cell.

A

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
Q

List and describe the three different mechanisms of endocytosis.

A
  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
Q

List and describe the two general pathways of exocytosis.

A
  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
Q

List and describe the four pathways for processing internalized ligand receptor
complexes

A
  1. receptor recycled, ligand degraded
  2. receptor and ligand recycled
  3. receptor and ligand degraded
  4. receptor and ligand transcytosis
44
Q

Explain the histologic basis of lysosomal storage diseases.

A
  • mutations in genes that code lysosomal enzymes
  • have increased undigested products
  • disruption of normal cell function
  • cell death
45
Q

Describe Tay-Sachs disease.

A
  • deficient in HEXA (B hexosaminidase A, ALPHA subunit
  • have accumulation of GM2 gangliosides
  • result: death of neurons in brain and spinal cord
46
Q

Describe diseases related to nonfunctional peroxisomes and Zellweger syndrome.

A
  • Nonfunctional peroxisomes cause abnormal myelination of nerve cells
    ie: Zellweger syndrome
47
Q

Describe Tay-Sachs disease.

A
  • deficient in HEXA (B hexosaminidase A, ALPHA subunit
  • have accumulation of GM2 gangliosides
  • result: death of neurons in brain and spinal cord
48
Q

Colchicine

A

Anticancer compound

  • prevents polymerization- binds to tubulin
  • mitotic spindle breaks down
  • apoptosis

related compounds - vinca akaloids

ie: vinblastin
- vinscristine

49
Q

Taxol

A

anticancer drug

  • stabilized and prevents microtubule assembly
  • bind tubulin within assembled microtubules
  • arrests cells in mitosis
  • apoptosis
  • cannot achieve metaphase spindle conformation
50
Q

Taxol

A

Anticancer drug

  • stabilized and prevents microtubule assembly
  • bind tubulin within assembled microtubules
  • arrests cells in mitosis
  • apoptosis
  • cannot achieve metaphase spindle conformation