Abstract
After axotomy of embryonic hippocampal neurons in vitro, some of the axotomized axons lose their identity, and new axons arise and grow. This axotomy-induced axonogenesis requires importin, suggesting that some injury-induced signals are transported via axons to elicit axonogenesis after axotomy. In this study, we show that STAT3 is activated in response to axotomy. Because STAT3 was co-immunoprecipitated with importin β in the axotomized neurons, we suggest that STAT3 is retrogradely transported as molecular cargo of importin α/β heterodimers. Indeed, inhibition of importin α binding with STAT3 resulted in the attenuation of axonogenesis. Silencing STAT3 blocked the axonogenesis, demonstrating that STAT3 is necessary for axotomyinduced axonogenesis. Furthermore, the overexpression of STAT3 enhanced axotomy-induced axonogenesis. Taken together, these results demonstrate that activation and retrograde transport of STAT3 in injured axons have key roles in the axotomyinduced axonogenesis of hippocampal neurons. © 2011 Macmillan Publishers Limited All rights reserved.
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Ohara, R., Fujita, Y., Hata, K., Nakagawa, M., & Yamashita, T. (2011). Axotomy induces axonogenesis in hippocampal neurons through STAT3. Cell Death and Disease, 2(6). https://doi.org/10.1038/cddis.2011.59
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