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Cited by 259

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Injury-Induced Decline of Intrinsic Regenerative Ability Revealed by Quantitative Proteomics

Open access
Belin, Stephane, Nawabi, Homaira, Wang, Chen, Tang, Shaojun, Latremoliere, Alban, Warren, Peter, Schorle, Hubert, Uncu, Ceren, Woolf, Clifford J., He, Zhigang, Steen, Judith A.·2015·Neuron

Abstract

Neurons differ in their responses to injury but the underlying mechanisms remain poorly understood. Using quantitative proteomics, we characterized the injury-triggered response from purified intact and axotomized retinal ganglion cells (RGCs). Subsequent informatics analyses revealed a network of injury-response signaling hubs. In addition to confirm known players, such as mTOR, this also identified new candidates, such as c-myc, NFkB and Huntingtin. Similar to mTOR, c-myc has been implicated as key regulators of anabolic metabolism and is down-regulated by axotomy. Forced expression of c-myc in RGCs, either before or after injury, promotes dramatic RGCs neuronal survival and axon regeneration after optic nerve injury. Finally, in contrast to RGCs, neither c-myc nor mTOR was down-regulated in injured peripheral sensory neurons. Our studies suggest that c-myc and other injury responsive pathways are critical to the intrinsic regenerative mechanisms and might represent a novel target for developing neural repair strategies in adults.

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Crossref · 10.1016/j.neuron.2015.03.060

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Metadata

Authors
Belin, S., Nawabi, H., Wang, C., Tang, S., Latremoliere, A., Warren, P., Schorle, H., Uncu, C., Woolf, C. J., He, Z., & Steen, J. A.
Venue
Neuron
Publisher
Elsevier BV
Published
2015-05
Volume
86
Issue
4
Pages
1000-1014
ISSN
0896-6273 (ISSN-L)
OpenAlex
W2028585054
Cited by
259
References
6
FWCI
10.17
Type
journal article
Language
en
Open access
bronze

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