Endogenous proBDNF is a negative regulator of migration of cerebellar granule cells in neonatal mice
@article{Xu2011EndogenousPI,
title={Endogenous proBDNF is a negative regulator of migration of cerebellar granule cells in neonatal mice},
author={Zhi-qiang Xu and Ying Sun and Hong-Yun Li and Yoon Lim and Jin-hua Zhong and Xin-Fu Zhou},
journal={European Journal of Neuroscience},
year={2011},
volume={33}
}The majority of newborn neurons migrate from their birthplace to final destination in the developing brain. Migration of cerebellar granule cells (CGCs) requires multiple factors. Mature brain‐derived neurotrophic factor (BDNF) positively regulates the proliferation, migration, survival and differentiation of CGCs in rodents. However, the role of the BDNF precursor, proBDNF, in neuronal development remains unknown. In this study, we investigated the effect of proBDNF in vivo and in vitro on…
52 Citations
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It is shown that proBDNF collapses neurite outgrowth in murine dorsal root ganglion (DRG) neurons and cortical neurons by activating RhoA via the p75 neurotrophin receptor (p75NTR).
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A role for MMP-3 is reported in the histogenesis of the mouse cerebellar cortex and neuronal migration anomalies seem to be caused by an abnormal PC dendritogenesis, which results in reducedPC dendritic trees in the adult cerebellum.
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The proBDNF signaling pathway is a potential novel therapeutic target for reducing sensory neuron and SGC loss following peripheral nerve injury and induced mitochondrial apoptosis in SGCs and sensory neurons in DRG following SNT.
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proBDNF may inhibit the neuronal viability and neurite growth via p75NTR, and it was found that the neurite length in proBDNF group was significantly shorter than that in control group.
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