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在机械应力存在的情况下,结缔组织生长因子参与转化生长因子β1对肌成纤维细胞分化和胶原基质收缩的刺激作用。

Involvement of CTGF in TGF-beta1-stimulation of myofibroblast differentiation and collagen matrix contraction in the presence of mechanical stress.

作者信息

Garrett Qian, Khaw Peng T, Blalock Timothy D, Schultz Gregory S, Grotendorst Gary R, Daniels Julie T

机构信息

Wound Healing Research Unit, Institute of Ophthalmology, London, United Kingdom.

出版信息

Invest Ophthalmol Vis Sci. 2004 Apr;45(4):1109-16. doi: 10.1167/iovs.03-0660.

Abstract

PURPOSE

This study was undertaken to investigate the role of connective tissue growth factor (CTGF) in fibroblast-to-myofibroblast differentiation and fibroblast-mediated collagen matrix contraction in the presence of mechanical stress.

METHODS

An in vitro three-dimensional contraction model of human corneal-fibroblast-seeded collagen lattices (FSCLs) in the presence of mechanical stress generated by attaching the lattices to the culture well was used to measure FSCL contraction. FSCLs were treated with CTGF; TGF-beta1; serum-free (SF) control medium; or TGF-beta1 plus antisense oligodeoxynucleotides to CTGF; TGF-beta1 plus scrambled-sequence oligodeoxynucleotide to CTGF; or TGF-beta antibody. Expression of alpha-smooth muscle actin (alpha-SMA) by fibroblasts in FSCLs was detected by immunostaining and confocal microscopy, whereas ELISA was used for the fibroblasts cultured on plastic. The conditioned media were analyzed by ELISA for CTGF production.

RESULTS

Exogenous CTGF stimulated significantly less collagen matrix contraction and myofibroblast differentiation than TGF-beta1, but similar to that stimulated by SF. TGF-beta1 stimulated fibroblasts to express CTGF. CTGF antisense oligodeoxynucleotide inhibited TGF-beta1-stimulated myofibroblast differentiation and FSCL contraction. Exogenous CTGF circumvented the inhibitory effects of CTGF antisense on FSCL contraction. TGF-beta antibody significantly inhibited FSCL contraction and myofibroblast differentiation under mechanical stress and SF control conditions.

CONCLUSIONS

In the presence of mechanical stress, CTGF is necessary for TGF-beta1-stimulation of myofibroblast differentiation and subsequent collagen matrix contraction, but CTGF alone is not sufficient to induce myofibroblast differentiation and collagen matrix contraction. Thus, TGF-beta1 appears to regulate multiple genes that are essential for fibroblast-mediated contraction of stressed matrix, one of which is CTGF.

摘要

目的

本研究旨在探讨在机械应力存在的情况下,结缔组织生长因子(CTGF)在成纤维细胞向肌成纤维细胞分化以及成纤维细胞介导的胶原基质收缩中的作用。

方法

使用一种体外三维收缩模型,即通过将接种人角膜成纤维细胞的胶原晶格(FSCLs)附着于培养孔产生机械应力,来测量FSCLs的收缩情况。FSCLs分别用CTGF、转化生长因子-β1(TGF-β1)、无血清(SF)对照培养基处理;或用TGF-β1加CTGF反义寡脱氧核苷酸处理;TGF-β1加CTGF乱序寡核苷酸处理;或用TGF-β抗体处理。通过免疫染色和共聚焦显微镜检测FSCLs中成纤维细胞α-平滑肌肌动蛋白(α-SMA)的表达,而酶联免疫吸附测定(ELISA)用于检测在塑料上培养的成纤维细胞。通过ELISA分析条件培养基中CTGF的产生情况。

结果

外源性CTGF刺激产生的胶原基质收缩和肌成纤维细胞分化明显少于TGF-β1,但与SF刺激的情况相似。TGF-β1刺激成纤维细胞表达CTGF。CTGF反义寡脱氧核苷酸抑制TGF-β1刺激的肌成纤维细胞分化和FSCL收缩。外源性CTGF可规避CTGF反义寡核苷酸对FSCL收缩的抑制作用。在机械应力和SF对照条件下,TGF-β抗体显著抑制FSCL收缩和肌成纤维细胞分化。

结论

在机械应力存在的情况下,CTGF是TGF-β1刺激肌成纤维细胞分化及随后胶原基质收缩所必需的,但单独的CTGF不足以诱导肌成纤维细胞分化和胶原基质收缩。因此,TGF-β1似乎调节多个对成纤维细胞介导的应激基质收缩至关重要的基因,其中之一就是CTGF。

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