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角膜上皮细胞中的SPARC可调节角膜细胞的胶原收缩。

SPARC from corneal epithelial cells modulates collagen contraction by keratocytes.

作者信息

Mishima H, Hibino T, Hara H, Murakami J, Otori T

机构信息

Department of Ophthalmology, Kinki University School of Medicine, Osaka-Sayama City, Osaka, Japan.

出版信息

Invest Ophthalmol Vis Sci. 1998 Dec;39(13):2547-53.

PMID:9856764
Abstract

PURPOSE

Contraction of the scar tissue during corneal wound healing changes the shape of the cornea and corneal refraction. In a previous study, it was found that corneal epithelial cells secrete the factor that stimulates collagen gel contraction by keratocytes in vitro. The purpose of the present study was to purify and identify the contraction-stimulating factor derived from corneal epithelial cells.

METHODS

The cultured medium of rabbit corneal epithelial cells was collected and used as an epithelial cell-conditioned medium (ECCM). Subcultured rabbit keratocytes were embedded in a collagen gel, and collagen gel contraction was investigated. The contraction-stimulating factor in the ECCM was purified through acetone precipitation, affinity chromatography (heparin Sepharose), gel filtration, and reversed-phase chromatography. The amino acid sequence of a contraction-stimulating factor was analyzed.

RESULTS

Collagen gel contraction by keratocytes was enhanced by the addition of ECCM in a dose-dependent manner. The amino acids sequence of the contraction-stimulating factor was homologous to a 32-kDa glycoprotein, a secreted protein that is acidic and rich in cysteine (SPARC). Western blot analysis confirmed that SPARC was contained in the ECCM. Collagen gel contraction by keratocytes was enhanced by the addition of purified SPARC in a dose-dependent manner. SPARC was found in the basal layer of the migrating epithelium and activated keratocytes adjacent to the wound 3 days and 1 week after perforating injury in rabbit corneas.

CONCLUSIONS

Epithelial cells secrete SPARC, which modulates the contraction of scar tissue in the corneal stroma.

摘要

目的

角膜伤口愈合过程中瘢痕组织的收缩会改变角膜形状和角膜屈光。在先前的一项研究中,发现角膜上皮细胞分泌一种因子,该因子在体外可刺激角膜细胞引起胶原凝胶收缩。本研究的目的是纯化并鉴定源自角膜上皮细胞的收缩刺激因子。

方法

收集兔角膜上皮细胞的培养液并用作上皮细胞条件培养基(ECCM)。将传代培养的兔角膜细胞包埋于胶原凝胶中,研究胶原凝胶收缩情况。通过丙酮沉淀、亲和层析(肝素琼脂糖)、凝胶过滤和反相层析对ECCM中的收缩刺激因子进行纯化。分析收缩刺激因子的氨基酸序列。

结果

加入ECCM后,角膜细胞引起的胶原凝胶收缩呈剂量依赖性增强。收缩刺激因子的氨基酸序列与一种32 kDa的糖蛋白、一种酸性且富含半胱氨酸的分泌蛋白(SPARC)同源。蛋白质印迹分析证实ECCM中含有SPARC。加入纯化的SPARC后,角膜细胞引起的胶原凝胶收缩呈剂量依赖性增强。在兔角膜穿孔伤后3天和1周,在迁移上皮的基底层和伤口附近活化的角膜细胞中发现了SPARC。

结论

上皮细胞分泌SPARC,其可调节角膜基质中瘢痕组织的收缩。

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