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干扰素对人二倍体成纤维细胞胶原蛋白合成的选择性抑制作用。

Selective inhibition of human diploid fibroblast collagen synthesis by interferons.

作者信息

Jimenez S A, Freundlich B, Rosenbloom J

出版信息

J Clin Invest. 1984 Sep;74(3):1112-6. doi: 10.1172/JCI111480.

Abstract

The effects of alpha- and gamma-interferons (IFNs) on collagen production by confluent human diploid fibroblasts in culture were examined. It was found that partially purified alpha-IFNs and affinity purified gamma-IFNs caused greater than 50% inhibition of collagen synthesis by these cells independently of their effect on cell proliferation. Recombinant alpha-IFNs showed a similar effect (38.8% inhibition), indicating that collagen synthesis inhibition was a constitutive property of IFNs. Collagen synthesis inhibition by IFNs was concentration dependent. Gel filtration chromatography of the newly synthesized proteins from the media of fibroblasts incubated with partially purified alpha-IFNs demonstrated a selective depression of molecules eluting in the region of procollagen. No detectable increase in collagen degradation products or underhydroxylation of procollagen was observed. Short-term kinetic studies further demonstrated that the major effect of IFNs was due to a net decrease in fibroblast collagen production rather than to impairment of secretion or increased extracellular degradation of the newly synthesized molecules. These results indicate that alpha- and gamma-IFNs are potent inhibitors of human fibroblast collagen production and suggest that they may play an important role in the regulation of normal and pathologic fibrogenesis.

摘要

研究了α-干扰素和γ-干扰素(IFNs)对培养的汇合人二倍体成纤维细胞胶原蛋白产生的影响。发现部分纯化的α-干扰素和亲和纯化的γ-干扰素对这些细胞胶原蛋白合成的抑制作用超过50%,且与其对细胞增殖的影响无关。重组α-干扰素显示出类似的效果(抑制38.8%),表明胶原蛋白合成抑制是干扰素的固有特性。干扰素对胶原蛋白合成的抑制作用呈浓度依赖性。对用部分纯化的α-干扰素孵育的成纤维细胞培养基中新合成蛋白质进行凝胶过滤层析,结果显示在原胶原区域洗脱的分子有选择性减少。未观察到胶原蛋白降解产物有可检测到的增加,也未观察到原胶原羟基化不足。短期动力学研究进一步表明,干扰素的主要作用是由于成纤维细胞胶原蛋白产生净减少,而非新合成分子的分泌受损或细胞外降解增加。这些结果表明,α-干扰素和γ-干扰素是人类成纤维细胞胶原蛋白产生的有效抑制剂,并提示它们可能在正常和病理性纤维生成的调节中发挥重要作用。

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本文引用的文献

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Lymphokine modulation of fibroblast proliferation.
J Immunol. 1982 Mar;128(3):1484-6.
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