| Literature DB >> 28614709 |
Anand N Rao1, Ankita Patil1, Mark M Black2, Erin M Craig3, Kenneth A Myers4, Howard T Yeung3, Peter W Baas5.
Abstract
Axonal microtubules are predominantly organized into a plus-end-out pattern. Here, we tested both experimentally and with computational modeling whether a motor-based polarity-sorting mechanism can explain this microtubule pattern. The posited mechanism centers on cytoplasmic dynein transporting plus-end-out and minus-end-out microtubules into and out of the axon, respectively. When cytoplasmic dynein was acutely inhibited, the bi-directional transport of microtubules in the axon was disrupted in both directions, after which minus-end-out microtubules accumulated in the axon over time. Computational modeling revealed that dynein-mediated transport of microtubules can establish and preserve a predominantly plus-end-out microtubule pattern as per the details of the experimental findings, but only if a kinesin motor and a static cross-linker protein are also at play. Consistent with the predictions of the model, partial depletion of TRIM46, a protein that cross-links axonal microtubules in a manner that influences their polarity orientation, leads to an increase in microtubule transport.Entities:
Keywords: TRIM46; axon; cytoplasmic dynein; microtubule; microtubule polarity orientation; microtubule sliding; microtubule transport; neuron
Mesh:
Substances:
Year: 2017 PMID: 28614709 PMCID: PMC5523108 DOI: 10.1016/j.celrep.2017.05.064
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423