Cytoskeleton & Cell Signaling Flashcards
Discuss the concept of a cytoskeleton.
The cytoskeleton is a dynamic intracellular structure (or set of structures) thatprovides cell shape, mechanical strength, the structures needed for locomotion, support for the plasma membrane, the scaffold for the spatial organization of organelles, and the means for intracellular transport of organelles and other cargo.The cytoskeleton is formed by three different families of proteins: microfilaments, microtubules, and intermediate filaments.
Describe microtubule and intermediate filament cytoskeleton (their properties, their functional roles, and their protein composition).
Microtubule: Alpha/Beta tubulin dimer, tubular structure 25nm in diameter, used for movement (flagella, cilia), cell organization, movement of organelles, cell division.Intermediate filament: Complex rope, 10nm in diameter, made of vimentin, keratin, and neurofilaments, used for mechanical stability.
Discuss cytoskeletal dynamics and the role of certain proteins and drugs in tubulin polymerization/depolymerization.
Colchicine inhibits MT polymerization. Vinblastine and vincristine also are MT polymerization blockers, derived from the Madagascar periwinkle (Vinca rosea).Paclitaxel (Taxol) was first isolated from the Pacific yew tree and also binds to MTs, but it stabilizes them, which causes tubule and tubulin aggregates. These compounds and their derivatives block mitosis and, thus, are of great interest for cancer treatment.
Explain the concept of molecular motor.Explain the mechanisms of tubulin-based movement and intracellular transport.
Many organelles (vesicles, mitochondria) travel long distances within cells, using MTs as tracks”. This is possible in conjunction with microtubule motor proteins. These proteins can transform the energy from ATP hydrolysis into a ‘walking’ motion along MTs
Discuss the role of microtubules in mitosis.
The mitotic spindle is constructed from MTs and associated proteins and serves to segregate the replicated chromosomes during mitosis.Three types of MTs can be distinguished: astral MTs” that radiate out from the centrosomes; “kinetochore MTs” that are attached to the kinetochore formed at the centromere of each duplicated chromosome; and “overlap MTs” that interdigitate at the equator of the spindle.In all cases
What do cilia and flagella do?Where are they found?
Cilia and flagella are wide-spread, hair-like cellular appendages that have a uniform diameter and contain a MT core, the axoneme.Flagella are long and serve to propel sperm by their undulating motion.Cilia are shorter and tend to occur in large numbers on the apical surface of various epithelial cells, especially those of the respiratory tract. By beating with a whip-like motion (across the cell surface) they move fluids over the surfaces of cells.In the respiratory tract, this serves to move dust particles, bacteria and mucus towards the mouth for elimination.Primary cilia or monocilia occur singly in a great variety of cells and may or may not be motile. Non-motile primary cilia serve special sensory functions, as photoreceptors (outer segment), chemosensors (e.g., in olfactory neurons), or mechanosensors.
What is an axoneme, its structure, and how does it move?
The axoneme can be 10-200nm long and consists of MTs and their associated proteins arranged as a ring of 9 special doublets (one complete plus one partial MT each) surrounding a pair of single MTs (9 + 2 array).Accessory proteins hold the array together, and axonemes are anchored in basal bodies.Axoneme bending results from the action of dynein. The motor action of dynein heads causes MTs to slide against one another. Because MTs are anchored to one another dynein action results in bending.Highly coordinated dynein activity in the axoneme causes flagellar waves or ciliary beating motion.
Discuss the cytoskeleton in the context of disease processes.
Trouble with cilia can cause numerous diseases, one being polycystic kidney disease.Microtubules are an important drug target in chemotherapy.Trouble with intermediate filaments can cause Charcot Marie Tooth disease and epidermolysis. The list goes on…
Discuss cytoskeletal dynamics and the role of certain proteins in actin filament formation, polymerization/depolymerization.
Arp2/3 + Formin start nucleation and seed the growth of actin. Arp2/3 makes tree like actin spindles while Formin seeds parallel spindles.Profilin (a protein) promotes polymerization on the plus end by converting ADP to ATP (in complex with G-actin).Capping proteins prevent the + end from growing and the - end from depolymerization.Cofilin severs the actin chain in half leading to depolymerization.
Understand the role of actin cytoskeleton in epithelial cell polarity and discuss some diseases associated with that.
One of the most important functions of actin is anchoring proteins that are involved in Tight junction (TJ) and Adherens junction (AJ) formation. Decreased association of AJ proteins (cadherins and catenins) with actin leads to internalization of cadherins and loss of cell-cell adhesion, the step that is a prerequisite for epithelial-to-mesenchimal (EMT) transition and cancer formation.In addition, actin plays a key role in apical micorvilli formation. All actin plus-ends are anchored in the apical protein cap of the microvillus. Actin bundles are held together by the cross-linking proteins villin and fimbrin, and bundles are linked laterally to the plasma membrane by myosin-I.Loss of microvilli is observed in microvilli inclusion disease.
Explain the concept of molecular motor. Explain the mechanism of actin-based organelle movement and muscle contraction.
Actin-binding motor proteins belong to the myosin family. Myosins (heavy chain) consist of a head region, which hyrdolyzes ATP to ADP. After hydrolyzing ATP the myosin head stretches towards and binds further down the + end of the actin tube. ATP then binds again and the cycle repeats. This is the power stroke.The ATP-driven walk of myosin heads along actin filaments results in the sliding-filament mechanism responsible for muscle contraction.Other non-conventional myosins, such as I and V, are associated with membranes and, thus, are involved in the F-actin-mediated movement of organelles.
Discuss the concept and the key steps of cell movement.
During locomotion, amoeboid cells go through repeated cycles of protrusion (of lamellipodia, filopodia), attachment (of these protrusions), traction (to pull the cell forward), and detachment (of adhesion toward the rear).Tight coordination between actin cytoskeleton dynamics and cell adhesion is a prerequisite for migration.
Discuss cell motility in the context of developmental and disease processes.
Lissencephaly: This is a severe defect of brain development resulting in a smooth cortical surface. Neuronal migration is a critical process for establishing the normal, complex cytoarchitecture of the brain. Loss-of-function of n-cofilin, an actin filament depolymerizing factor, results in lissencephaly and the associated severe mental retardation.Metastasis: Most of the terminal cancers are characterized by the spread of the tumors from the primary site (metastasis).
Understand the role of actomyosin ring in cell division.
Actin plays a key role in cytokinesis. The formation and contraction of actomyosin ring drives the formation of the cleavage furrow and separation of the daughter cells.The site of actomyosin ring formation and the timing of its contraction are highly regulated events that determine the symmetry of cell division.
Understand the mechanisms regulating the establishment and activation of actomyoisn ring.
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