Functional identification of neuroprotective molecules.

Functional identification of neuroprotective molecules.
复制标题

DOI:
10.1371/journal.pone.0015008
复制
发表时间:
2010-11-24
期刊:
影响因子:
3.7
通讯作者:
Dawson VL
Dawson VL
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Dai C;Liang D;Li H;Sasaki M;Dawson TM;Dawson VL

文献摘要

参考文献

被引文献

相似文献

在亚致命应激后,中枢神经系统具有激活深层神经保护的能力,这一过程被称为预适应。为了深入了解这种有效的生存反应,我们开发了一种功能克隆策略,鉴定了31个假定的神经保护基因,其中28个被证实对原代大鼠皮质神经元的缺氧-葡萄糖剥夺(OGD)或N-甲基-D-天冬氨酸(NMDA)兴奋毒性暴露具有保护作用。这些结果表明,大脑拥有广泛而多样的神经保护基因库。对这些和其他保护性信号的进一步表征可能会为缺血或神经退行性疾病造成的神经损伤提供新的治疗机会。
The central nervous system has the capacity to activate profound neuroprotection following sub-lethal stress in a process termed preconditioning. To gain insight into this potent survival response we developed a functional cloning strategy that identified 31 putative neuroprotective genes of which 28 were confirmed to provide protection against oxygen-glucose deprivation (OGD) or excitotoxic exposure to N-methyl-D-aspartate (NMDA) in primary rat cortical neurons. These results reveal that the brain possesses a wide and diverse repertoire of neuroprotective genes. Further characterization of these and other protective signals could provide new treatment opportunities for neurological injury from ischemia or neurodegenerative disease.
DOI: 10.1242/jcs.037051
发表时间: 2009-02-01
影响因子: 4
作者:
Naslavsky, Naava;McKenzie, Jenna;Caplan, Steve
通讯作者: Caplan, Steve
DOI: 10.1073/pnas.0611609104
发表时间: 2007-03-06
影响因子: 11.1
作者:
Huang, Yunfei;Higginson, Daniel S.;Snyder, Solomon H.
通讯作者: Snyder, Solomon H.
DOI: 10.1042/bst0371293
发表时间: 2009-12-01
影响因子: 3.9
作者:
Abbott, Catherine M.;Newbery, Helen J.;Soares, Dinesh C.
通讯作者: Soares, Dinesh C.
DOI: 10.1074/jbc.m211684200
发表时间: 2003-02-28
影响因子: 4.8
作者:
Moon, YA;Horton, JD
通讯作者: Horton, JD
DOI: 10.1042/bj20061817
发表时间: 2007-08-15
影响因子: 4.1
作者:
Wahab, Nadia;Cox, Dimity;Mason, Roger M.
通讯作者: Mason, Roger M.