Paz Soldán M Mateo, Warrington Arthur E, Bieber Allan J, Ciric Bogoljub, Van Keulen Virginia, Pease Larry R, Rodriguez Moses
Program in Molecular Neuroscience, Mayo Medical and Graduate Schools, 200 First Street SW, Rochester, MN 55905, USA.
Mol Cell Neurosci. 2003 Jan;22(1):14-24. doi: 10.1016/s1044-7431(02)00018-0.
Our laboratory has identified mouse and human monoclonal antibodies that promote myelin repair in multiple models of demyelinating disease. We have proposed that these antibodies promote remyelination by directly activating central nervous system glia. Intracellular calcium concentration was monitored using a Fura2 ratiometric assay. Repair-promoting antibodies induced distinct Ca2+ signals in both astrocytes and oligodendrocytes. Astrocyte Ca2+ signaling is mediated by a phospholipase C-dependent pathway while oligodendrocyte Ca2+ signaling is mediated via AMPA-sensitive glutamate receptors. An antibody's ability to induce Ca2+ signals is statistically correlated with promotion of myelin repair. These findings support the hypothesis that remyelination-promoting antibodies are acting directly at the surface of glial cells to induce calcium-dependent physiologic reparative function.
我们的实验室已经鉴定出在多种脱髓鞘疾病模型中促进髓鞘修复的小鼠和人单克隆抗体。我们提出这些抗体通过直接激活中枢神经系统胶质细胞来促进髓鞘再生。使用Fura2比率测定法监测细胞内钙浓度。促进修复的抗体在星形胶质细胞和少突胶质细胞中均诱导出不同的Ca2+信号。星形胶质细胞的Ca2+信号传导由磷脂酶C依赖性途径介导,而少突胶质细胞的Ca2+信号传导则通过AMPA敏感的谷氨酸受体介导。抗体诱导Ca2+信号的能力与髓鞘修复的促进作用在统计学上相关。这些发现支持了促进髓鞘再生的抗体直接作用于胶质细胞表面以诱导钙依赖性生理修复功能的假说。