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• W1900179675 abstract "One major mechanism of cell-mediated cytolysis is the polarized secretion of lytic granules, a process which is highly dependent on microtubules. We isolated lytic granules from murine cytotoxic T cells and tested their ability to bind to and move along microtubules in vitro. In the presence of a motor-containing supernatant, the granules bound to the microtubules and moved along them at an average maximal rate of 1 microns/second. Virtually every granule could bind to microtubules, and about half translocated within a few seconds of binding. Motility required exogenous cytosolic motors, hydrolyzable nucleotides, and an intact granule membrane. Although the motor preparation used to support granule movement contains both plus- and minus-end-directed motor proteins, granule movement was strongly biased toward microtubule plus-ends. Inactivation of cytoplasmic dynein had little effect on granule binding and movement, but immuno-depletion of kinesin from the motor preparation inhibited granule binding by 50%. These results indicate that most granule movement in this assay is mediated by kinesin. The speed and direction of granule movement in vitro are sufficient to account for the release of lytic granules in the intact T cell. This model system should be valuable for studying the interactions of secretory granules with microtubules, and for identifying the regulatory factors involved." @default.
• W1900179675 created "2016-06-24" @default.
• W1900179675 creator A5039653234 @default.
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• W1900179675 creator A5077637690 @default.
• W1900179675 creator A5083812073 @default.
• W1900179675 date "1993-01-01" @default.
• W1900179675 modified "2023-10-09" @default.
• W1900179675 title "Lytic granules from cytotoxic T cells exhibit kinesin-dependent motility on microtubules in vitro" @default.
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• W1900179675 doi "https://doi.org/10.1242/jcs.104.1.151" @default.
• W1900179675 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8449993" @default.
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