Roulois A J A, Zhao C, Zawadzka M, Bruce C C, Franklin R J M
Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge.
Rev Neurol (Paris). 2007 Jun;163(6-7):667-71. doi: 10.1016/s0035-3787(07)90477-4.
Although the treatment of multiple sclerosis has made significant strides in the last decade, successful translation from laboratory to clinical medicine of neuronal repair remains a therapeutic challenge. Nevertheless, advances in the biology of stem and precursor cells, particularly in relation to myelin damage, make this a realistic proposition during the next decade. Replacing lost myelin (remyelination) is currently thought to be an important clinical objective because of the role it might play in slowing or preventing axonal degeneration. Stem/precursor cell-based strategies for enhancing remyelination can be divided into those in which cell are transplanted into a patients (exogenous or cell therapies) and those in which the patients own stem/precursor cells are mobilised to more efficiently engage in healing areas of demyelination (endogenous or pharmacological therapies). While the two approaches tend to be regarded separately they are not mutually exclusive. This article focuses on the endogenous approach and reviews the nature and nomenclature of the stem and precursor cells present within the adult CNS that engage in remyelination and that are therefore potential targets for pharmacological manipulation.
尽管在过去十年中,多发性硬化症的治疗取得了重大进展,但将神经元修复从实验室成功转化为临床医学仍然是一项治疗挑战。然而,干细胞和前体细胞生物学的进展,特别是与髓鞘损伤相关的进展,使得在未来十年内实现这一目标成为一个现实的命题。由于重新形成髓鞘(髓鞘再生)可能在减缓或预防轴突变性中发挥作用,目前认为它是一个重要的临床目标。基于干细胞/前体细胞的促进髓鞘再生的策略可分为将细胞移植到患者体内的策略(外源性或细胞疗法)以及动员患者自身的干细胞/前体细胞更有效地参与脱髓鞘愈合区域的策略(内源性或药物疗法)。虽然这两种方法往往被分开看待,但它们并非相互排斥。本文重点关注内源性方法,并综述了成年中枢神经系统中参与髓鞘再生、因此是药物操纵潜在靶点的干细胞和前体细胞的性质及命名。