SOCS3 and Optic Nerve Regeneration in Zebrafish

Daniel Goldman, PhD
Regents of the University of Michigan (Ann Arbor, MI)
Year Awarded:
Grant Duration:
April 1, 2006 to March 31, 2008
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US Midwestern
Recipient of the Thomas R. Lee award for National Glaucoma Research

SOCS3 and Optic Nerve Regeneration in Zebrafish


Glaucoma often leads to blindness due to optic nerve damage and retinal ganglion cell death. Optic nerve regeneration may restore vision in patients suffering from glaucoma. Unfortunately the damaged mammalian optic nerve does not readily regenerate. Interestingly, fish regenerate their optic nerve following damage and therefore provide an ideal system for studying the mechanisms underlying successful optic nerve regeneration. In a recent screen for genes that might mediate successful optic nerve regeneration in zebrafish, Dr. Goldman has identified suppressor of cytokine signaling 3 (SOCS3), which is highly induced in retinal ganglion cells that are regenerating their optic axons. SOCS3 is a multifunctional SOCS protein that not only modulates the immune response, but can also influence a number of signal transduction cascades that impact cell survival and axon outgrowth. In this grant application he proposes to test whether SOCS3 is essential for successful optic nerve regeneration. This will be accomplished by knocking down the expression of SOCS3 in adult retinal ganglion cells whose optic axons have been lesioned and assaying cell survival and optic axon regeneration in vivo.


Veldman, M. B., Bemben, M. A., Thompson, R. C. and Goldman, D. Gene expression analysis of zebrafish retinal ganglion cells during optic nerve regeneration identifies KLF6a and KLF7a as important regulators of axon regeneration. Developmental Biology, 2007; 312:596-612.  

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