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1
MOUVEMENT-Centriole-Centrosome-Kinetochore-Axonène-Cellule ciliée
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a. Dimerization of a and b tubulin subtypes
b. Linear repitition of the heterodimers makes a
a b - a b - a b - a b - a b - a b - a b - a b - a b - a btubulin protofilament growingMicrotubule organizing
center
c. Side-by-side assembly of 13 protofilaments to make a sheet
d. Rolling of the sheet into a tubule
MICROTUBULE CONSTRUCTION
e. Elongationcontrolled by[ions] [a b ]GTP GDP rate
Colchicine blocks elongation
CB subfibersA
101013protofilaments
BUILD A CENTRIOLE or BASAL BODY
Assemble 2 partial & onecomplete microtubules intoa TRIPLET
Arrange 9 triplets in parallel &position an identical array nearby& perpendicular
CENTROSOME = 2 Centrioles +Microtubule Organizing Center
CENTRIOLES - MTOC -KINETOCHORES
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• The cell cycle and mitosis: mechanism (example)
nonkinetochoremicrotubule
kinetochoremicrotubules
BsubfibersA
1013protofilaments
MICROTUBULES BUILD AN AXONEME of cilium or flagellum
Extend A & B subfibers to be the axoneme’s doublets
9 doublets
Other microtubule arrays arethe MITOTIC SPINDLE &AXONAL CORE
central pair
The axoneme has a 9 double MT + 2 center MT patternwith dynein arms on the outside for sliding action!
This is the “Sliding Filament Theory”
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MICROTUBULES FOR THE CILIARY BEAT
Dynein arm with ATPaseactivity to power movement -generating a sliding interactionwith B subfiber of adjacentmicrotubule doublet
Connections turn the microtubulesliding into BENDING of the Cilium
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MICROTUBULES FOR THE CILIARY BEAT
MEDICAL CORRELATIONSA genetic axonemal dynein deficiency impairs ciliary clearance ofthe airway, leading to severe lung infections of Kartegener’ssyndrome
Dangerous cell proliferation in cancer can be halted by vinblastinewhich blocks mitotic spindle formation
Dynein arm with ATPaseactivity to power movement -generating a sliding interactionwith B subfiber of adjacentmicrotubule doublet
Connections turn the microtubulesliding into BENDING of the Cilium
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GOLGI
Zonula occludens
Zonula adherens
Macula adherens/Desmosome
Hemi-desmosome
BL
.
Keratin Intermediate Filaments
Centrioles & MTOCfor Microtubules
luminal
basal
lateral
Actin cortex
Basal bodies
CILIUM9 + 2 Microtubular array (9 doublets)
with 9 + 0 array (9 triplets)
CILIATED AIRWAY CELL
SENSORY STEREOCILIA ON AUDITORY HAIR CELL
Actin filaments
bundled, as the as thecore of the stereocilium
meshwork, as anchoringcuticular plate
Ion channelsopened bydeflection ofstereocilium
Synapses
Stereocilia arenon-motile,but can bemoved by thestimulus
SENSORY STEREOCILIA ON AUDITORY HAIR CELL
Actin filamentscore of the stereocilium
meshwork
Stereocilia arenon-motile,but can bemoved by thestimulus
Hair cell alsohas a solitarytall truecilium, withmicrotubules
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SENSORY STEREOCILIA ON AUDITORY HAIR CELL
Actin filaments
bundled, as the as thecore of the stereocilium
Ion channels
Synapses
meshwork
& Stereociliaare non-motile
Note: nomicrotubules in thesignal-transductionmechanism
So why the‘cilium’ name?
Why, indeed!
Dynein arms move acrossadjacent MTs and cause
sliding and axonemalbendingmotion
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CELL SHAPES
1 Cylindrical/columnar, cuboidal, polyhedral, flattened epithelial cell shapes to fit into multicellular patterns
2 Spheroid & Ovoid - defensive blood cells
3 Elongated - muscle cells & fibroblasts
4 Multiple branching processes - neurons, glial cells, pigment cells
Generalization
Microtubules and intermediate filaments with cell junctionshold shape and polarization
Actin microfilaments (with & without myosin) modify shape
VARIETIES OF MOVEMENT
Ciliary & Flagellar
Intracellular vesicles
Chromatids during mitosis
Whole cell (sperm)
by MICROTUBULES
Whole cell
Extension of processes
Separation of cells at mitosis
Intracellular vesicles
by ACTIN FILAMENTS
GeneralizationsLittle direct motor role for Intermediate FilamentsMicrotubules & IFs highly concentrated around the nucleus &extend radially; actin more peripheral under the plasmalemma inthe “cortex” Exceptions are: muscle, neurons, mature epidermal cells, RBCs
Movements are closely related to cell’s shape & polarity