| Literature DB >> 26898779 |
Vijayendran Chandran1, Giovanni Coppola2, Homaira Nawabi3, Takao Omura3, Revital Versano1, Eric A Huebner3, Alice Zhang4, Michael Costigan3, Ajay Yekkirala3, Lee Barrett3, Armin Blesch5, Izhak Michaelevski6, Jeremy Davis-Turak1, Fuying Gao7, Peter Langfelder8, Steve Horvath8, Zhigang He3, Larry Benowitz3, Mike Fainzilber6, Mark Tuszynski5, Clifford J Woolf3, Daniel H Geschwind9.
Abstract
The regenerative capacity of the injured CNS in adult mammals is severely limited, yet axons in the peripheral nervous system (PNS) regrow, albeit to a limited extent, after injury. We reasoned that coordinate regulation of gene expression in injured neurons involving multiple pathways was central to PNS regenerative capacity. To provide a framework for revealing pathways involved in PNS axon regrowth after injury, we applied a comprehensive systems biology approach, starting with gene expression profiling of dorsal root ganglia (DRGs) combined with multi-level bioinformatic analyses and experimental validation of network predictions. We used this rubric to identify a drug that accelerates DRG neurite outgrowth in vitro and optic nerve outgrowth in vivo by inducing elements of the identified network. The work provides a functional genomics foundation for understanding neural repair and proof of the power of such approaches in tackling complex problems in nervous system biology.Entities:
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Year: 2016 PMID: 26898779 PMCID: PMC4790095 DOI: 10.1016/j.neuron.2016.01.034
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173