Kobayashi Tatsuya, Inoue Tsutomu, Okada Hirokazu, Kikuta Tomohiro, Kanno Yoshihiko, Nishida Takashi, Takigawa Masaharu, Sugaya Takeshi, Suzuki Hiromichi
Department of Nephrology, Saitama Medical College, 38 Morohongo, Moroyama-machi, Saitama 350-0495, Japan.
Clin Exp Nephrol. 2005 Jun;9(2):114-21. doi: 10.1007/s10157-005-0347-x.
It was reported that connective tissue growth factor (CTGF) was expressed in the tubular epithelial cells of the diabetic kidney. CTGF has, among other factors, been implicated in mediating the downstream, profibrotic effects of transforming growth factor-beta (TGF-beta), though is precise role in interstitial fibrogenesis in the diabetic kidney has not yet been clarified.
We employed a coculture system involving cultured murine proximal tubular epithelial cells (mProx24) and renal fibroblasts (TFB), as a model of the subepithelial mesenchyme in the kidney in order to examine the profibrotic effects of CTGF derived from mProx24 cells in response to high glucose (30 mM).
We showed that glucose stimulated CTGF expression in cultured mProx24 in both a dose- and a time-dependent manner, and that this effect was mediated by increased levels of TGF-beta. We also found that high glucose significantly stimulated TFB cells to produce profibrotic molecules, such as type I collagen, the EIIIA isoform of fibronectin, and plasminogen activator inhibitor-1. The induction of these molecules was both direct and indirect, the latter induction being mediated by mProx24 cell-derived CTGF, which, in turn, was induced by TGF-beta that was produced by the mProx24 cells.
CTGF plays an important role in mediating renal interstitial fibrogenesis in response to high glucose and, as such, is a reasonable target for anti-fibrotic therapy.
据报道,结缔组织生长因子(CTGF)在糖尿病肾病的肾小管上皮细胞中表达。CTGF在诸多因素中,被认为介导了转化生长因子-β(TGF-β)的下游促纤维化作用,尽管其在糖尿病肾病间质纤维化中的精确作用尚未阐明。
我们采用一种共培养系统,该系统包含培养的小鼠近端肾小管上皮细胞(mProx24)和肾成纤维细胞(TFB),以此作为肾脏上皮下间质的模型,来研究mProx24细胞来源的CTGF在高糖(30 mM)刺激下的促纤维化作用。
我们发现葡萄糖以剂量和时间依赖性方式刺激培养的mProx24中CTGF的表达,且这种作用是由TGF-β水平升高介导的。我们还发现高糖显著刺激TFB细胞产生促纤维化分子,如I型胶原、纤连蛋白的EIIIA异构体和纤溶酶原激活物抑制剂-1。这些分子的诱导既有直接作用也有间接作用,后者是由mProx24细胞来源的CTGF介导的,而mProx24细胞来源的CTGF又是由mProx24细胞产生的TGF-β诱导产生的。
CTGF在介导高糖诱导的肾间质纤维化中起重要作用,因此是抗纤维化治疗的合理靶点。