@article {1302192,
	title = {IGFBPL1 Regulates Axon Growth through IGF-1-mediated Signaling Cascades},
	journal = {Sci Rep},
	volume = {8},
	number = {1},
	year = {2018},
	month = {2018 Feb 01},
	pages = {2054},
	abstract = {Activation of axonal growth program is a critical step in successful optic nerve regeneration following injury. Yet the molecular mechanisms that orchestrate this developmental transition are not fully understood. Here we identified a novel regulator, insulin-like growth factor binding protein-like 1 (IGFBPL1), for the growth of retinal ganglion cell (RGC) axons. Expression of IGFBPL1 correlates with RGC axon growth in development, and acute knockdown of IGFBPL1 with shRNA or IGFBPL1 knockout in vivo impaired RGC axon growth. In contrast, administration of IGFBPL1 promoted axon growth. Moreover, IGFBPL1 bound to insulin-like growth factor 1 (IGF-1) and subsequently induced calcium signaling and mammalian target of rapamycin (mTOR) phosphorylation to stimulate axon elongation. Blockage of IGF-1 signaling abolished IGFBPL1-mediated axon growth, and vice versa, IGF-1 required the presence of IGFBPL1 to promote RGC axon growth. These data reveal a novel element in the control of RGC axon growth and suggest an unknown signaling loop in the regulation of the pleiotropic functions of IGF-1. They suggest new therapeutic target for promoting optic nerve and axon regeneration and repair of the central nervous system.},
	issn = {2045-2322},
	doi = {10.1038/s41598-018-20463-5},
	author = {Guo, Chenying and Cho, Kin-Sang and Li, Yingqian and Tchedre, Kissauo and Antolik, Christian and Ma, Jie and Chew, Justin and Utheim, Tor Paaske and Huang, Xizhong A and Yu, Honghua and Malik, Muhammad Taimur A and Anzak, Nada and Chen, Dong Feng}
}
