Guo An-Chen, Chu Takho, Liu Xu-Qing, Su Huan-Xing, Wu Wu-Tian
Department of Anatomy, Li Ka Shing Faculty of Medicine, The University of Hong KongPokfulam, Hong Kong SAR, China; Laboratory of Clinical Medical Research, Beijing Tiantan Hospital, Capital Medical UniversityBeijing, China; Key Laboratory of Translational Medicine for Cerebrovascular DiseaseBeijing, China.
Research Center of Reproduction, Development and Growth, Li Ka Shing Faculty of Medicine, The University of Hong Kong Pokfulam, Hong Kong SAR, China.
Am J Transl Res. 2016 Dec 15;8(12):5637-5645. eCollection 2016.
Multiple sclerosis (MS) is ademyelinating disease in the central nervous system (CNS). Majority of the MS patients show relapsing-remitting disease course. Evidences show that oligodendrocyte precursor cells (OPCs), which remain relatively quiescent in normal adult CNS, play a key role in the remitting phase by proliferation and remyelination. In the present study, we found that spinal cord astrocytesco-expressed progenitor cell marker and oligodendroglial lineage markers in the remittance phase in adult rat experimental autoimmune encephalomyelitis (EAE) model. We suggest that activated astrocyte could de-differentiate into OPCs and re-differentiate into mature oligodendrocytes, raising the possibility that astrocytes can be a potential source of OPCs in the adult demyelinated spinal cord.
多发性硬化症(MS)是一种中枢神经系统(CNS)的脱髓鞘疾病。大多数MS患者表现为复发缓解型病程。有证据表明,少突胶质前体细胞(OPCs)在正常成年中枢神经系统中相对静止,在缓解期通过增殖和再髓鞘化发挥关键作用。在本研究中,我们发现成年大鼠实验性自身免疫性脑脊髓炎(EAE)模型脊髓星形胶质细胞在缓解期共表达祖细胞标志物和少突胶质谱系标志物。我们认为,活化的星形胶质细胞可去分化为OPCs并再分化为成熟少突胶质细胞,这增加了星形胶质细胞可能是成年脱髓鞘脊髓中OPCs潜在来源的可能性。