• Huaxiang Liu, Guixiang Liu, and Yanwen Bi.
• Department of Rheumatology, Shandong University Qilu Hospital, Jinan 250012, China.
• Neurosci. Lett. 2014 May 21;569:110-5.

AbstractHIV envelope glycoprotein gp120 is highly involved in HIV infection-related peripheral neuropathy, but its mechanism remains incompletely understood. The therapy of this neuropathy is still a big clinical challenge for neurologists. The organotypically cultured dorsal root ganglion (DRG) explants were used to test the neurotoxic actions of gp120 and the therapeutic effects of ciliary neurotrophic factor (CNTF) on gp120-induced neurotoxicity. The results showed that gp120 inhibited neurite outgrowth and neuronal migration from the DRG explants in a dose-dependent manner. HIV-gp120 also inhibited growth-associated protein 43 (GAP-43) expression and induced apoptosis of the migrating neurons. CNTF improved neurite outgrowth, neuronal migration, and GAP-43 expression inhibited by gp120. CNTF also rescued neuronal apoptosis induced by gp120. Either Janus kinase 2 (JAK2) inhibitor AG490 or phosphatidyl inositol-3'-phosphate-kinase (PI3K) inhibitor LY294002 blocked the effects of CNTF. These data imply that CNTF improved neuronal status by promoting GAP-43 expression and inhibiting apoptosis through JAK2/signal transducer and activator of transcription 3 (STAT3) and PI3K/Akt signaling pathways of DRG neurons with gp120-induced neurotoxicity. These data offered a new clue for elucidating the mechanisms of HIV infection-related peripheral neuropathy and facilitating the development of novel therapy.Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

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