A chemical genetic approach reveals distinct EphB signaling mechanisms during brain development

被引:0
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作者
Michael J Soskis
Hsin-Yi Henry Ho
Brenda L Bloodgood
Michael A Robichaux
Athar N Malik
Bulent Ataman
Alex A Rubin
Janine Zieg
Chao Zhang
Kevan M Shokat
Nikhil Sharma
Christopher W Cowan
Michael E Greenberg
机构
[1] Harvard Medical School,Department of Neurobiology
[2] University of Texas Southwestern Medical Center,Department of Psychiatry
[3] University of California,Department of Cellular and Molecular Pharmacology
[4] Present address: Department of Chemistry,undefined
[5] University of Southern California,undefined
[6] Los Angeles,undefined
[7] California,undefined
[8] USA (C.Z.),undefined
[9] Department of Psychiatry,undefined
[10] McLean Hospital,undefined
[11] Harvard Medical School,undefined
[12] Belmont,undefined
[13] Massachusetts,undefined
[14] USA (C.W.C.).,undefined
来源
Nature Neuroscience | 2012年 / 15卷
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摘要
The EphB family of receptor tyrosine kinases can signal bidirectionally and functions in a kinase-dependent and kinase-independent manner. To determine the importance of the kinase activity of EphBs for axonal guidance and synaptogenesis, the authors used a chemical genetic method and generated knock-in mice that allow the kinase activity of EphBs to be inhibited without altering kinase-independent functions of EphBs. They find that specific inhibition of EphB kinase activity had no effect on synaptogenesis, but impaired axonal guidance, thereby implicating the kinase function of EphB in one neuronal process, but not other processes that are nevertheless dependent on EphBs.
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页码:1645 / 1654
页数:9
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