Opposite-polarity motors activate one another to trigger cargo transport in live cells

被引:167
作者
Ally, Shabeen [1 ]
Larson, Adam G. [1 ]
Barlan, Kari [1 ]
Rice, Sarah E. [1 ]
Gelfand, Vladimir I. [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Cell & Mol Biol, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
TUG-OF-WAR; FAST AXONAL-TRANSPORT; CYTOPLASMIC DYNEIN; MICROTUBULE MOTORS; KINESIN EG5; INTRACELLULAR-TRANSPORT; VESICLE TRANSPORT; MOLECULAR MOTORS; IN-VITRO; XENOPUS MELANOPHORES;
D O I
10.1083/jcb.200908075
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intracellular transport is typically bidirectional, consisting of a series of back and forth movements. Kinesin-1 and cytoplasmic dynein require each other for bidirectional transport of intracellular cargo along microtubules; i.e., inhibition or depletion of kinesin-1 abolishes dynein-driven cargo transport and vice versa. Using Drosophila melanogaster S2 cells, we demonstrate that replacement of endogenous kinesin-1 or dynein with an unrelated, peroxisome-targeted motor of the same directionality activates peroxisome transport in the opposite direction. However, motility-deficient versions of motors, which retain the ability to bind microtubules and hydrolyze adenosine triphosphate, do not activate peroxisome motility. Thus, any pair of opposite-polarity motors, provided they move along microtubules, can activate one another. These results demonstrate that mechanical interactions between opposite-polarity motors are necessary and sufficient for bidirectional organelle transport in live cells.
引用
收藏
页码:1071 / 1082
页数:12
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