Microtubule (MT) organization is essential for many cellular events, including mitosis, migration, and cell polarity. Fidgetin (Fign), an ATP-dependent, MT-severing protein, contributes to the regulation of MT configuration by cutting and trimming MT polymers. Functions of Fign have been indicated in neurite outgrowth, mitosis, meiosis, and cellular migration. Here we focus on migration of astrocytes. We find that Fign plays an essential role in cultured astrocyte migration by preferentially targeting MTs (or regions of MTs) that are rich in tyrosinated tubulin, a marker for especially dynamic MTs or especially dynamic regions of MTs. Inhibition of cellular migration induced by Fign knockdown can be rescued with concomitant knockdown of kinesin-12, a motor protein best known for its role in mitosis. We propose a novel working model for MT reconfiguration underlying cellular migration elicited by the functional cooperation of two distinct MT-related proteins.
Fidgetin regulates cultured astrocyte migration by severing tyrosinated microtubules at the leading edge
Creators
Zunlu Hu - Nantong University
Jie Feng - Nantong University
Weijuan Bo - Nantong University
Ronghua Wu - Nantong University
Zhangji Dong - Nantong University
Yan Liu - Key Laboratory of Neuroregeneration, Jiangsu, and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu 226001, China
Liang Qiang - Nantong University
Mei Liu - Nantong University
Publication Details
Molecular biology of the cell, v 28(4), pp 545-553
Resource Type
Journal article
Language
English
Academic Unit
Neurobiology and Anatomy
Web of Science ID
WOS:000394270800005
Scopus ID
2-s2.0-85013276097
Other Identifier
991019168419804721
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