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Publication : Lack of the transcription factor C/EBPδ impairs the intrinsic capacity of peripheral neurons for regeneration.

First Author  Lopez de Heredia L Year  2013
Journal  Exp Neurol Volume  239
Pages  148-57 PubMed ID  23099414
Mgi Jnum  J:196991 Mgi Id  MGI:5490432
Doi  10.1016/j.expneurol.2012.10.012 Citation  Lopez de Heredia L, et al. (2013) Lack of the transcription factor C/EBPdelta impairs the intrinsic capacity of peripheral neurons for regeneration. Exp Neurol 239:148-57
abstractText  Adult neurons of the peripheral nervous system (PNS), in contrast to those of the central nervous system, have a remarkable capacity to repair themselves after injury, yet the mechanisms underlying this regenerative propensity of peripheral neurons are far from completely understood. Here we show that the transcription factor CCAAT enhancer binding protein delta (C/EBPdelta) is necessary for the efficient axonal regeneration of dorsal root ganglia (DRG) neurons after sciatic nerve crush injury. Loss of C/EBPdelta substantially impairs axonal growth in dissociated cultured DRG neurons. In addition, lack of C/EPBdelta causes a major reduction in the regenerative response of DRG neurons to a conditioning lesion, which is a well known paradigm of injury that enhances axonal growth due to a transcription-dependent cell body response. C/EBPdelta is required for the induction of selected regeneration-associated genes. For example, the expression of SPRR1A (small proline-rich repeat protein 1A) is greatly reduced in DRG neurons of C/EBPdelta knockout mice during axonal regeneration compared to those in wild-type mice, while the expression of GAP-43 (growth associated protein-43) and galanin is not affected. Nevertheless, the expected prompt recovery of sciatic nerve function after injury is severely impaired in C/EBPdelta knockout mice, having a delay time of approximately 1 month for reaching the full function of recovering wild-type mice, suggesting that a transcription mechanism mediated by C/EBPdelta is required for efficient axonal regeneration. Taken together, our results identify C/EBPdelta as a crucial component of the transcriptional regulatory machinery which underlies the intrinsic capacity of peripheral neurons for axonal regeneration.
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