期刊文献+
共找到1篇文章
< 1 >
每页显示 20 50 100
Phosphatidylserine improves axonal transport by inhibition of HDAC and has potential in treatment of neurodegenerative diseases 被引量:2
1
作者 Shiran Naftelberg gil ast Eran Perlson 《Neural Regeneration Research》 SCIE CAS CSCD 2017年第4期534-537,共4页
Familial dysautonomia (FD) is a rare children neurodegenerative disease caused due to a point mutation in the IKBKAP gene that results in decreased IKK complex-associated protein (IKAP) protein production. The dis... Familial dysautonomia (FD) is a rare children neurodegenerative disease caused due to a point mutation in the IKBKAP gene that results in decreased IKK complex-associated protein (IKAP) protein production. The disease affects mostly the dorsal root ganglion (DRG) and the sympathetic ganglion. Recently, we found that the molecular mechanisms underlying neurodegeneration in FD patients are defects in axonal transport of nerve growth factors and microtubule stability in the DRG. Neurons are highly polarized cells with very long axons. In order to survive and maintain proper function, neurons depend on transport of proteins and other cellular components from the neuronal body along the axons. We further demonstrated that IKAP is necessary for axon maintenance and showed that phosphatidylserine acts as an HDAC6 inhib- itor to rescue neuronal function in FD cells. In this review, we will highlight our latest research findings. 展开更多
关键词 axonaI transport NEURODEGENERATION MICROTUBULE familial dysautonomia PHOSPHATIDYLSERINE HDAC6
暂未订购
上一页 1 下一页 到第
使用帮助 返回顶部