Schwab J M, Postler E, Nguyen T D, Mittelbronn M, Meyermann R, Schluesener H J
Institute of Brain Research, University of Tuebingen, Medical School, Tuebingen, Germany.
Neuropathol Appl Neurobiol. 2000 Oct;26(5):434-40. doi: 10.1046/j.1365-2990.2000.00271.x.
Connective tissue growth factor (CTGF), a transforming growth factor (TGF)-beta1 downstream mediator, is a secreted cell matrix-inducing peptide involved in both tissue regeneration mechanisms, such as wound repair, and also in aberrant deposition of extracellular matrix. The present study reports CTGF expression by cells associated with matrix deposition and glial scar formation in human cerebral infarction. CTGF was localized by immunohistochemistry in 17 brains of patients after focal infarction and in three neuropathologically normal control brains. CTGF expression was selectively localized to the cytoplasm of stellate reactive astrocytes. Compared to peripheral areas and brain controls without neuropathological findings, the total number CTGF+ astrocytes was significantly higher (P < 0.0001) in border zones adjacent to the core, corresponding to the penumbra. These numbers were significantly increased at day 1 and day 3 and remained persistently elevated up to several months post-infarction (P < 0.0001). The restricted expression and accumulation of CTGF+ reactive astrocytes adds convincing evidence for CTGF participation in the gliotic astrocyte CNS injury response involved in glial scar formation. CTGF can be considered a sensitive marker of early human astrocyte activation and a possible target for pharmacological intervention of aberrant matrix deposition.
结缔组织生长因子(CTGF)是转化生长因子(TGF)-β1的下游介质,是一种分泌性细胞基质诱导肽,参与组织再生机制,如伤口修复,也参与细胞外基质的异常沉积。本研究报道了CTGF在人类脑梗死中与基质沉积和胶质瘢痕形成相关的细胞中的表达情况。通过免疫组织化学方法,在17例局灶性梗死患者的脑以及3例神经病理学正常的对照脑中定位了CTGF。CTGF表达选择性地定位于星状反应性星形胶质细胞的细胞质中。与周边区域和无神经病理学发现的脑对照相比,梗死核心相邻的边界区域(对应于半暗带)中CTGF+星形胶质细胞的总数显著更高(P < 0.0001)。这些数量在第1天和第3天显著增加,并且在梗死后数月内持续升高(P < 0.0001)。CTGF+反应性星形胶质细胞的局限性表达和积累为CTGF参与胶质瘢痕形成所涉及的胶质细胞CNS损伤反应提供了令人信服的证据。CTGF可被视为早期人类星形胶质细胞活化的敏感标志物以及异常基质沉积药物干预的可能靶点。