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The microtubule cytoskeleton is required for a G2 cell cycle delay in cancer cells lacking stathmin and p53
Author(s) -
Carney Bruce K.,
Caruso Silva Victoria,
Cassimeris Lynne
Publication year - 2012
Publication title -
cytoskeleton
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.95
H-Index - 86
eISSN - 1949-3592
pISSN - 1949-3584
DOI - 10.1002/cm.21024
Subject(s) - stathmin , nocodazole , mitosis , biology , microbiology and biotechnology , interphase , cell cycle , tubulin , microtubule , cytoskeleton , cell , biochemistry
In several cancer cell lines, depleting the microtubule (MT)‐destabilizing protein stathmin/oncoprotein18 leads to a G2 cell cycle delay and apoptosis. These phenotypes are observed only in synergy with low levels of p53, but the pathway(s) activated by stathmin depletion to delay the cell cycle are unknown. We found that stathmin depletion caused greater MT stability in synergy with loss of p53, measured by the levels of acetylated α‐tubulin and the rate of centrosomal MT nucleation. Nocodazole or vinblastine‐induced MT depolymerization abrogated the stathmin‐depletion induced G2 delay, measured by the percentage of cells staining positive for several markers (TPX2, CDK1 with inhibitory phosphorylation), indicating that MTs are required to lengthen G2. Live cell imaging showed that stathmin depletion increased time in G2 without an impact on the duration of mitosis, indicating that the longer interphase duration is not simply a consequence of a previous slowed mitosis. In contrast, stabilization of MTs with paclitaxel (8 nM) slowed mitosis without lengthening the duration of interphase, demonstrating that increased MT stability alone is not sufficient to delay cells in G2. © 2012 Wiley Periodicals, Inc