4.7 Article

Activation of Rac GTPase by p75 is necessary for c-jun N-terminal kinase-mediated apoptosis

Journal

JOURNAL OF NEUROSCIENCE
Volume 22, Issue 1, Pages 156-166

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.22-01-00156.2002

Keywords

apoptosis; Rac GTPase; c-jun N-terminal kinase; signal transduction; p75; NGF

Categories

Funding

  1. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS039472] Funding Source: NIH RePORTER
  2. NINDS NIH HHS [R01 NS039472, R01 NS39472-01] Funding Source: Medline

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The neurotrophin receptor p75 can induce apoptosis both in vitro and in vivo. The mechanisms by which p75 induces apoptosis have remained mostly unknown. Here, we report that p75 activates Rac GTPase, which in turn activates c-jun N-terminal kinase (JNK), including an injury-specific JNK3, in an NGF-dependent manner. N17Rac blocks this JNK activation and subsequent NGF-dependent apoptosis, indicating that activation of Rac GTPase is required for JNK activation and apoptosis induced by p75. In addition, p75-mediated Rac activation is modulated by coactivation of Trk, identifying Rac GTPase as one of the key molecules whose activity is critical for cell survival and death in neurotrophin signaling. The crucial role of the JNK pathway in p75 signaling is further confirmed by the results that blocking p75 from signaling via the JNK pathway or suppressing the JNK activity itself led to inhibition of NGF-dependent death. Together, these results indicate that the apoptotic machinery of p75 comprises Rac GTPase and JNK.

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