Inhibition of clathrin by pitstop 2 activates the spindle assembly checkpoint and induces cell death in dividing HeLa cancer cells

被引:39
作者
Smith, Charlotte M. [1 ]
Haucke, Volker [2 ,3 ]
McCluskey, Adam [4 ]
Robinson, Phillip J. [1 ]
Chircop, Megan [1 ,5 ]
机构
[1] Univ Sydney, Childrens Med Res Inst, Westmead, NSW 2145, Australia
[2] Free Univ Berlin, Inst Chem & Biochem, D-14195 Berlin, Germany
[3] Leibniz Inst Mol Pharmakol FMP, Berlin, Germany
[4] Univ Newcastle, Sch Environm & Life Sci, Callaghan, NSW 2308, Australia
[5] Childrens Med Res Inst, Wentworthville, NSW 2145, Australia
基金
英国医学研究理事会;
关键词
Clathrin; Pitstop; Spindle assembly checkpoint; Metaphase; Cell death; Cancer; AURORA-A KINASE; MEDIATED ENDOCYTOSIS; CYTOKINESIS FAILURE; TERMINAL DOMAIN; MITOTIC SPINDLES; DYNAMIN; PHOSPHORYLATION; CENTROSOME; DIVISION; TACC3;
D O I
10.1186/1476-4598-12-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: During metaphase clathrin stabilises the mitotic spindle kinetochore(K)-fibres. Many anti-mitotic compounds target microtubule dynamics. Pitstop 2 (TM) is the first small molecule inhibitor of clathrin terminal domain and inhibits clathrin-mediated endocytosis. We investigated its effects on a second function for clathrin in mitosis. Results: Pitstop 2 did not impair clathrin recruitment to the spindle but disrupted its function once stationed there. Pitstop 2 trapped HeLa cells in metaphase through loss of mitotic spindle integrity and activation of the spindle assembly checkpoint, phenocopying clathrin depletion and aurora A kinase inhibition. Conclusions: Pitstop 2 is therefore a new tool for investigating clathrin spindle dynamics. Pitstop 2 reduced viability in dividing HeLa cells, without affecting dividing non-cancerous NIH3T3 cells, suggesting that clathrin is a possible novel anti-mitotic drug target.
引用
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页数:15
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