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Ca2+-dependent regulation of rho GTPases triggers turning of nerve growth cones.


ABSTRACT: Cytoplasmic Ca2+ elevation and changes in Rho GTPase activity are both known to mediate axon guidance by extracellular factors, but the causal relationship between these two events has been unclear. Here we show that direct elevation of cytoplasmic Ca2+ by extracellular application of a low concentration of ryanodine, which activated Ca2+ release from intracellular stores, upregulated Cdc42/Rac, but downregulated RhoA, in cultured cerebellar granule cells and human embryonic kidney 293T cells. Chemoattractive turning of the growth cone triggered by a gradient of ryanodine was blocked by overexpression of mutant forms of Cdc42 but not of RhoA in Xenopus spinal cord neurons. Furthermore, Ca2+-induced GTPase activity correlated with activation of protein kinase C and required a basal activity of Ca2+/calmodulin-dependent protein kinase II. Thus, Rho GTPases may mediate axon guidance by linking upstream Ca2+ signals triggered by guidance factors to downstream cytoskeletal rearrangements.

SUBMITTER: Jin M 

PROVIDER: S-EPMC6726106 | biostudies-literature | 2005 Mar

REPOSITORIES: biostudies-literature

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Ca2+-dependent regulation of rho GTPases triggers turning of nerve growth cones.

Jin Ming M   Guan Chen-bing CB   Jiang Yun-ai YA   Chen Gang G   Zhao Chun-tao CT   Cui Kai K   Song Yuan-quan YQ   Wu Chien-ping CP   Poo Mu-ming MM   Yuan Xiao-bing XB  

The Journal of neuroscience : the official journal of the Society for Neuroscience 20050301 9


Cytoplasmic Ca2+ elevation and changes in Rho GTPase activity are both known to mediate axon guidance by extracellular factors, but the causal relationship between these two events has been unclear. Here we show that direct elevation of cytoplasmic Ca2+ by extracellular application of a low concentration of ryanodine, which activated Ca2+ release from intracellular stores, upregulated Cdc42/Rac, but downregulated RhoA, in cultured cerebellar granule cells and human embryonic kidney 293T cells. C  ...[more]

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