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Inhibitory molecules associated with myelin and the glial scarlimit axon regeneration in the adult central nervous system(CNS), but the underlying signaling mechanisms of regenerationinhibition are not fully understood. Here, we show that suppressingthe kinase function of the epidermal growth factor receptor(EGFR) blocks the activities of both myelin inhibitors and chondroitinsulfate proteoglycans in inhibiting neurite outgrowth. In addition,regeneration inhibitors trigger the phosphorylation of EGFRin a calcium-dependent manner. Local administration of EGFRinhibitors promotes significant regeneration of injured opticnerve fibers, pointing to a promising therapeutic avenue forenhancing axon regeneration after CNS injury.
1 Division of Neuroscience, Children's Hospital, Boston, MA 02115, USA. 2 Schepens Eye Research Institute, Department of Ophthalmology, Harvard Medical School, Boston, MA 02114, USA. 3 Division of Research, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
* To whom correspondence should be addressed. E-mail: zhigang.he{at}childrens.harvard.edu
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