Disconnecting the Golgi ribbon from the centrosome prevents directional cell migration and ciliogenesis

被引:115
作者
Hurtado, Lidia [1 ]
Caballero, Cristina [1 ]
Gavilan, Maria P. [1 ]
Cardenas, Jesus [1 ]
Bornens, Michel [2 ]
Rios, Rosa M. [1 ]
机构
[1] Consejo Super Invest Cient, Ctr Andaluz Biol Mol & Med Regenerat, Dept Senalizac Celular, Seville 41092, Spain
[2] Inst Curie, Ctr Natl Rech Sci, Unite Mixte Rech 144, F-75252 Paris 05, France
关键词
CG-NAP; MICROTUBULE NUCLEATION; SCAFFOLDING PROTEIN; REGULATES GOLGI; MOTILE CELLS; COMPLEX; ORGANIZATION; APPARATUS; AKAP450; NETWORK;
D O I
10.1083/jcb.201011014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian cells exhibit a frequent pericentrosomal Golgi ribbon organization. In this paper, we show that two AKAP450 N-terminal fragments, both containing the Golgi-binding GM130-interacting domain of AKAP450, dissociated endogenous AKAP450 from the Golgi and inhibited microtubule (MT) nucleation at the Golgi without interfering with centrosomal activity. These two fragments had, however, strikingly different effects on both Golgi apparatus (GA) integrity and positioning, whereas the short fragment induced GA circularization and ribbon fragmentation, the large construct that encompasses an additional p150glued/MT-binding domain induced separation of the Golgi ribbon from the centrosome. These distinct phenotypes arose by specific interference of each fragment with either Golgi-dependent or centrosome-dependent stages of Golgi assembly. We could thus demonstrate that breaking the polarity axis by perturbing GA positioning has a more dramatic effect on directional cell migration than disrupting the Golgi ribbon. Both features, however, were required for ciliogenesis. We thus identified AKAP450 as a key determinant of pericentrosomal Golgi ribbon integrity, positioning, and function in mammalian cells.
引用
收藏
页码:917 / 933
页数:17
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