De Vries G H, Neuberger T J, Baichwal R R, Bigbee J W, Zane L, Yoshino J E
Department of Biochemistry and Molecular Biophysics, Medical College of Virginia, Richmond 23298-0614.
Ann N Y Acad Sci. 1993 May 28;679:217-25. doi: 10.1111/j.1749-6632.1993.tb18301.x.
The release of membrane-associated growth factors after neural injury may influence the outcome of the recovery. For example, for remyelination to occur after neural injury it is critical for the glial cell to proliferate prior to remyelination in both the PNS and CNS. In the CNS, the relative response of the oligodendrocytes and astroglia to growth factors mobilized during neural injury may play a role in the cellular dynamics of repair of neural injury or scarring and subsequent failure to repair neural injury. In support of this view, we have studied the mitotic potential and cell cycle kinetics of cultured adult oligodendrocytes and found that these adult cells respond only weakly to factors such as FGF which are known to be potent mitogens for neonatal cells. However, given the same dose of FGF, adult astrocytes are mitotically stimulated to a much greater degree than are the adult oligodendrocytes (Vick and De Vries, unpublished observations). Given the pathways which may be operative in the release of growth factors after injury, it has not escaped our attention that, provided the released factors are in equilibrium with easily accessible and peripheral body fluids, these released factors may serve as new markers for neural injury. Further experiments are in progress to explore this possibility.
神经损伤后膜相关生长因子的释放可能会影响恢复结果。例如,对于神经损伤后发生的髓鞘再生而言,在周围神经系统(PNS)和中枢神经系统(CNS)中,神经损伤后胶质细胞在髓鞘再生之前进行增殖至关重要。在中枢神经系统中,少突胶质细胞和星形胶质细胞对神经损伤期间动员的生长因子的相对反应,可能在神经损伤修复或瘢痕形成以及随后神经损伤修复失败的细胞动力学中发挥作用。为支持这一观点,我们研究了培养的成年少突胶质细胞的有丝分裂潜能和细胞周期动力学,发现这些成年细胞对诸如成纤维细胞生长因子(FGF)等已知对新生细胞有强大促有丝分裂作用的因子反应较弱。然而,给予相同剂量的FGF,成年星形胶质细胞比成年少突胶质细胞受到的有丝分裂刺激程度要大得多(维克和德弗里斯,未发表的观察结果)。鉴于损伤后生长因子释放可能涉及的途径,我们注意到,如果释放的因子与易于获取的外周体液处于平衡状态,这些释放的因子可能作为神经损伤的新标志物。进一步的实验正在进行中,以探索这种可能性。