IAS19

Question 1

unit membrane concept & plasma membrane staining

Answer 1

all cellular membranes have same underlying struc. & diff. functions
trilaminar shape, stained by osmium

Question 2

plasma membrane lipid components structure & movement

Answer 2

PP amphipathic, polar hydrophilic head facing outward, 2 nonpolar phobic tails facing inward
move laterally, rotate or flipflop
cholesterol interspersed among PP, determines fluid nature of membrane (more cholesterol, more interaction w/ FA chain, more rigid)

Question 3

plasma membrane other components

Answer 3

proteins
integral: part of membrane structure, cannot be removed w/o damaging the membrane
periphery: binds to either side of membrane, can easily be separated
carb: complex glycoproteins

Question 4

fluid mosaic model

Answer 4

fluidity: PP has high mobility
deg. of fluidity inc. w/ temp (dist. of PP & energy), shorter FA tail, more double bonds, less cholesterol
mosaic: proteins dispersed thruout membrane

Question 5

plasma membrane functions

Answer 5

C (BIR) SSCC compartmentalization: define boundaries, allows specialized activities to proceed w/o ext. interference & cellular activies to be regulated independently
scaffold for biochem activities
selective permeable barrier: allows some materials to pass but not others, allows nutrients to enter cell & wastes to exit
act as receptors to detect chem signals (trigger cellular activity cascade)
provide contact, adhesion & communication (cytoplasmic process exchange cellular components)

Question 6

cell membrane permeability

Answer 6

barrier to most water-soluble substances, selective perme. to lipid solvent, high resistance to charged & large molecules

Question 7

mitochondria & its membrane

Answer 7

provide energy & involved in apoptosis
double membrane: highly folded inner, smooth outer

Question 8

ER generally

Answer 8

double membrane bound
membrane runs cont. w/ outer membrane of nuclear envelope, lumen cont. w/ nuclear lumen

Question 9

ER types

Answer 9

rough: flattened sheets of membranes & tubules, ribosomes present for protein synthesis, span through whole cytoplasm, well-developed in protein synth. & secretory cells
proteins synthesized pass on to cisternae
smooth: no ribosomes, more tubular
for lipid synth.; detox in liver; Ca storage & release in muscles

Question 10

golgi apparatus

Answer 10

for modification, packing & distribution of proteins & lipids for secretion / internal use
stacked membranous, flattened cisternae w/ vesicles

Question 11

golgi faces & lumen

Answer 11

cis face receives transport vesicles budded from ER containing new proteins
lumen: protein & lipid modification, progression through transport vesicles budding off from each cisterna & fusing w/ the next
trans: mature proteins & lipids released as vesicles, contains condensing granules

Question 12

lysosome

Answer 12

single membrane bound
contain enzymes to degrade phagocytosed materials
destruction of organelles

Question 13

peroxisome

Answer 13

smaller ver. of lysosome
contain enzymes to break down long FA & amino acids forming H2O2 byproduct, contains catalase to neut. H2O2
common in liver for detox

Question 14

nucleus stain & nuclear envelope

Answer 14

stain in H&E: blue / purple (acidic, -vely charge) (cannot see membrane w/ H&E)
envelope: double membrane, pores form by fusion of both membranes
pores allow diffusion of small molecules, active import of proteins & rna from & into nucleus

Question 15

nucleoplasm

Answer 15

consist of DNA, nucleoproteins, etc.
contains chromatin (DNA & histones)
basophilic, heterogeneously stained

Question 16

types of chromatin

Answer 16

heterochromatin: dark stained, dense packed chromatin less active at gene transcription, at nuclear periphery
euchromatin: the reverse

Question 17

nucleolus

Answer 17

synthesis of rRNA, contains genes for encoding rRNA (chr 13 14 15 21 22)
process & assemble ribosomal subunits imported from CP -> transported out of nucleus

Question 18

nucleolus regions

Answer 18

fc: fibrillar center, palely stained, inactivated genes for transcription
dfc: dense fibrillar component, darkly stained, nascent pre-rRNA transcription, rRNA early modification
gc: granular component, occupies most of nucleolus, ribosomal subunit assembly at diff. stages

Question 19

cytoskeleton functions

Answer 19

microfilament, intermediate filament, microtubule (extend from centrosome to periphery)
1. maintains cell shape & used in locomotion
2. in cell division
3. guides intracellular traffic of organelles
4. provides mech strength

Question 20

microfilament & function

Answer 20

actin as building block, globular monomer g-actin polymerize to form long helical filamentous polymer f-actin
polar, + end grows faster than - end
used in muscle contraction, locomotion, cytokinesis & structural functions

Question 21

microfilament organization & contribution to movement

Answer 21

dynamically organised into bundles & networks, stabilized by interaction w/ diff. cross-linking proteins
some lie in cell cortex below plasma membrane, arranged in loose 3d mesh
in leading edge, microfilaments arranged in ||type bundles, spike-like protrusions formed by active polymerization of actin at tip of protrusion, allows movement & migration

Question 22

microfilament in cytokinesis

Answer 22

interacts w/ myosin, contracts cells through contractile ring (bundle)

Question 23

actin assembly in intestinal villi

Answer 23

actin filaments connected by actin-bundling protein fimbrin (CLP)
filaments extend down to apical cytoplasm to form network below microvilli bottom: terminal web, connected to microfilament core
stabilized by CLP filamin

Question 24

intermediate filament structure

Answer 24

bundled fibrous proteins
2 helical monomers twist to form dimer
2 dimers interact anti|| to form tetramer
tetramers assembled end to end to form protofilament

Question 25

intermediate filament function

Answer 25

3SA stronger than actin filament, exhibits strain hardening during stress -> structural / tension bearing role maintain cell shape & scaffold to support cell framework anchor organelles

Question 26

types of intermediate filament

Answer 26

keratin (epithelial cell), vimentin (connective tissue, smooth muscle), neurofilament (neuron), nuclear lamin (in nuclear lamina in inner nuclear membrane)

Question 27

keratin filament & defect

Answer 27

forms strong network within cells, connected w/ junctional complexes -> creating sheet of cells allowing to withstand phy force in cells in mutation (no keratin production) -> cells fragile & prone to rupture in little mech. stress, skin blistering in epidermis & during dermis

Question 28

microtubules structure

Answer 28

tubulin dimers (alpha, beta tubulin) -> polymerization in linear rows to form protofilament -> 13 protofilaments side-by-side to form hollow center dynamic: elongation at + end by polymerization, shortening at - end by depolymerization

Question 29

microtubules origination

Answer 29

microtubule organising center (MTOC) microtubule assembly initiated & acts as anchor for one end MTOC called centrosome in animal cell (2 centrioles near nucleus) MTOC in cilia & flagella called basal bodies, extend microtubules & push out plasma membrane to form cilia / flagella

Question 30

microtubule in mitosis

Answer 30

forms mitotic spindle to guide segregation of chromosome through shortening & extension

Question 31

microtubule in IC organelle transport

Answer 31

axonal transport: motor proteins carry chem. components in vesicles down the axon w/ help of microtubules -> released at axonal end to synaptic cleft kinesin moves toward + end dyenin moves toward - end

Question 32

agents that prevent microtubule function

Answer 32

colchicine, bind to microtubules to prevent polymerization taxol, bind to microtubules to prevent depolymerization -> affect dynamic process of mitotic spindle required for chromosomal separation -> disrupt mitosis & cell division both act as anti-mitotic drug to prevent cell proliferation