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1.
J Neurobiol ; 58(2): 189-200, 2004 Feb 05.
Article in English | MEDLINE | ID: mdl-14704951

ABSTRACT

Cytoplasmic dynein has long been thought to be responsible for retrograde axonal transport. As the number of cellular roles for this multifunctional protein has expanded, the complexity of its contribution to axonal transport has increased. In this article the increasing evidence for a role for cytoplasmic dynein in anterograde as well as retrograde transport is discussed. The current status of the complex dynein cargo-binding mechanism is evaluated. Finally, recent genetic evidence supporting a role in axonal transport and revealing a role in neurodegenerative conditions is reviewed.


Subject(s)
Axonal Transport/physiology , Dyneins/physiology , Models, Biological , Molecular Motor Proteins/physiology , Animals , Carrier Proteins/metabolism , Cytoplasm/metabolism , Dynactin Complex , Dyneins/chemistry , Microtubule-Associated Proteins/metabolism , Motor Neuron Disease , Protein Binding
2.
J Cell Biol ; 163(6): 1205-11, 2003 Dec 22.
Article in English | MEDLINE | ID: mdl-14691133

ABSTRACT

Cytoplasmic dynein has been implicated in numerous aspects of intracellular movement. We recently found dynein inhibitors to interfere with the reorientation of the microtubule cytoskeleton during healing of wounded NIH3T3 cell monolayers. We now find that dynein and its regulators dynactin and LIS1 localize to the leading cell cortex during this process. In the presence of serum, bright diffuse staining was observed in regions of active ruffling. This pattern was abolished by cytochalasin D, and was not observed in cells treated with lysophosphatidic acid, conditions which allow microtubule reorientation but not forward cell movement. Under the same conditions, using total internal reflection fluorescence microscopy, clear punctate dynein/dynactin containing structures were observed along the sides and at the tips of microtubules at the leading edge. Overexpression of dominant negative dynactin and LIS1 cDNAs or injection of antidynein antibody interfered with the rate of cell migration. Together, these results implicate a leading edge cortical pool of dynein in both early and persistent steps in directed cell movement.


Subject(s)
Cell Movement/physiology , Cytoplasm/metabolism , Dyneins/metabolism , Microtubule-Associated Proteins/metabolism , 1-Alkyl-2-acetylglycerophosphocholine Esterase , Animals , Antibodies/pharmacology , Blood Proteins/pharmacology , Chick Embryo , Cytochalasin D/metabolism , Cytochalasin D/pharmacology , Cytoskeleton/metabolism , Cytoskeleton/ultrastructure , DNA, Complementary/genetics , Dynactin Complex , Lysophospholipids/pharmacology , Mice , Microtubule-Associated Proteins/genetics , Microtubules/metabolism , Models, Biological , NIH 3T3 Cells , Pseudopodia/metabolism , Pseudopodia/ultrastructure , Wound Healing/genetics
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