Cai Junying, Hua Fuzhou, Yuan Linhui, Tang Wei, Lu Jun, Yu Shuchun, Wang Xifeng, Hu Yanhui
Department of Anesthesiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, China.
Department of Urology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, China.
Biomed Res Int. 2014;2014:601084. doi: 10.1155/2014/601084. Epub 2014 Apr 9.
The neurotrophins (NTs) nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), NT-3, and NT-4/5 are proteins that regulate cell proliferation, differentiation, and survival in both the developing and mature central nervous system (CNS) by binding to two receptor classes, Trk receptors and p75 NTR. Motivated by the broad growth- and survival-promoting effects of these proteins, numerous studies have attempted to use exogenous NTs to prevent the death of cells that are associated with neurological disease or promote the regeneration of severed axons caused by mechanical injury. Indeed, such neurotrophic effects have been repeatedly demonstrated in animal models of stroke, nerve injury, and neurodegenerative disease. However, limitations, including the short biological half-lives and poor blood-brain permeability of these proteins, prevent routine application from treating human disease. In this report, we reviewed evidence for the neuroprotective efficacy of NTs in animal models, highlighting outstanding technical challenges and discussing more recent attempts to harness the neuroprotective capacity of endogenous NTs using small molecule inducers and cell transplantation.
神经营养因子(NTs),即神经生长因子(NGF)、脑源性神经营养因子(BDNF)、NT-3和NT-4/5,是一类蛋白质,它们通过与两类受体(Trk受体和p75神经营养因子受体(p75 NTR))结合,在发育中和成熟的中枢神经系统(CNS)中调节细胞增殖、分化和存活。受这些蛋白质广泛的生长促进和存活促进作用的驱动,众多研究试图使用外源性NTs来防止与神经疾病相关的细胞死亡,或促进由机械损伤导致的切断轴突的再生。事实上,这种神经营养作用已在中风、神经损伤和神经退行性疾病的动物模型中反复得到证实。然而,这些蛋白质的生物半衰期短和血脑通透性差等局限性,阻碍了其在治疗人类疾病中的常规应用。在本报告中,我们回顾了NTs在动物模型中神经保护功效的证据,强调了突出的技术挑战,并讨论了利用小分子诱导剂和细胞移植来发挥内源性NTs神经保护能力的最新尝试。