نتایج جستجو برای: axon regeneration

تعداد نتایج: 79002  

Journal: :مجله علوم اعصاب شفای خاتم 0
marzieh darvishi a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran. b. department of anatomy, tarbiat modares university, tehran, iran. taghi tiraihi a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran. b. department of anatomy, tarbiat modares university, tehran, iran. taher taheri shefa neuroscience research center, khatam alanbia hospital, tehran, iran.

central nervous system axons fail to regenerate after spinal cord injury (sci), partially due to the accumulation of extracellular matrix molecules in the lesion and formation of the glial scar. depakine, as known as histone deacetylase inhibitor, has neuroprotective effects. this study evaluated the histological changes (cavitation and axon regeneration) after sci associated with (following ad...

Journal: :Neuron 2014
Alexandra B. Byrne Trent Walradt Kathryn E. Gardner Austin Hubbert Valerie Reinke Marc Hammarlund

The ability of injured axons to regenerate declines with age, yet the mechanisms that regulate axon regeneration in response to age are not known. Here we show that axon regeneration in aging C. elegans motor neurons is inhibited by the conserved insulin/IGF1 receptor DAF-2. DAF-2's function in regeneration is mediated by intrinsic neuronal activity of the forkhead transcription factor DAF-16/F...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Chin Lik Tan Jessica C F Kwok Rickie Patani Charles Ffrench-Constant Siddharthan Chandran James W Fawcett

Chondroitin sulfate proteoglycans (CSPGs) are upregulated after CNS lesions, where they inhibit axon regeneration. In order for axon growth and regeneration to occur, surface integrin receptors must interact with surrounding extracellular matrix molecules. We have explored the hypothesis that CSPGs inhibit regeneration by inactivating integrins and that forcing integrins into an active state mi...

2015
Peter W. Baas Andrew J. Matamoros

Microtubules have been identified as a powerful target for augmenting regeneration of injured adult axons in the central nervous system. Drugs that stabilize microtubules have shown some promise, but there are concerns that abnormally stabilizing microtubules may have only limited benefits for regeneration, while at the same time may be detrimental to the normal work that microtubules perform f...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2004
Jeffrey L Goldberg Mauricio E Vargas Jack T Wang Wim Mandemakers Stephen F Oster David W Sretavan Ben A Barres

In the mammalian CNS, glial cells repel axons during development and inhibit axon regeneration after injury. It is unknown whether the same repulsive axon guidance molecules expressed by glia and their precursors during development also play a role in inhibiting regeneration in the injured CNS. Here we investigate whether optic nerve glial cells express semaphorin family members and, if so, whe...

2010
Xiaodan JIANG Shengbin Kou Zhiqiang Fa Yehai Li Zhenzhou Chen Shanshan Song Hongbo GUO Yiquan KE Ruxiang XU Zhicheng XIAO

It was traditionally thought that the central nerve system (CNS) defects the regenerated ability, following the injury. However, the peripheral nerve system (PNS) possesses an ability of regeneration after injury. Also it was found that the axon in CNS might extend into the graft, as soon as the peripheral nerve tissue was transplanted into the injured part of CNS. Therefore, it implied that th...

Journal: :Nature Reviews Neuroscience 2006

Journal: :Molecular and Cellular Neuroscience 2010

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