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The Journal of Neuroscience, July 7, 2004, 24(27):6218-6227; doi:10.1523/JNEUROSCI.1692-04.2004

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Cellular/Molecular
Rapid Axoglial Signaling Mediated by Neuregulin and Neurotrophic Factors

Raymond M. Esper¹ and Jeffrey A. Loeb^1,2

¹Department of Neurology and ²Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201

During peripheral nervous system development, Schwann cells are precisely matched to the axons that they support. This is mediated by axonal neuregulins that are essential for Schwann cell survival and differentiation. Here, we show that sensory and motor axons rapidly release heparin-binding forms of neuregulin in response to Schwann cell-derived neurotrophic factors in a dose-dependent manner. Neuregulin release occurs within minutes, is saturable, and occurs from axons that were isolated using a newly designed chamber slide apparatus. Although NGF and glial cell line-derived neurotrophic factor (GDNF) were the most potent neurotrophic factors to release neuregulin from sensory neurons, GDNF and BDNF were most potent for motor neurons and were the predominant neuregulin-releasing neurotrophic factors produced by cultured Schwann cells. Comparable levels of neuregulin could be released at a similar rate from neurons after protein kinase C activation with the phorbol ester, phorbol 12-myristate 13-acetate, which has also been shown to promote the cleavage and release of neuregulin from its transmembrane precursor. The rapid release of neuregulin from axons in response to Schwann cell-derived neurotrophic factors may be part of a spatially restricted system of communication at the axoglial interface important for proper peripheral nerve development, function, and repair.

Key words: neuregulin; neurotrophin; GDNF; Schwann cell; axon; protein kinase

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Received Dec 19, 2003; revised May 27, 2004; accepted May 28, 2004.

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