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可溶性因子在博来霉素诱导的肺纤维化中的作用。

The role of soluble factors in bleomycin-induced pulmonary fibrosis.

作者信息

Phan S H, Thrall R S

出版信息

Am J Pathol. 1982 Feb;106(2):156-64.

Abstract

Endotracheal administration of bleomycin causes pulmonary fibrosis characterized by increased collagen synthesis and deposition. Incubation of normal lung mince with neutral salt soluble extracts of lungs from normal and bleomycin-treated rats caused a dose-dependent inhibition of collagen and noncollagenous protein synthesis. Bleomycin-treated lung extracts, however, were significantly less effective in such inhibition when compared with normal lung extracts. This inhibitory activity was not diminished by dialysis in tubing with nominal molecular weight cutoff of 10,000 but was destroyed by heat (70 C) and trypsin digestion. This inhibitory activity could not be ascribed to residual serum or bleomycin in the lung extracts. Fractionation on Sephacryl S-200 (Pharmacia, Piscataway, NJ) showed inhibitory activity to be heterogeneous with Mr (apparent molecular weight) greater than 100,000. Extracts from spleen showed similar inhibitory activity but showed no difference in intensity between normal and bleomycin-treated spleen. These data suggest that loss or decrease in production of lung inhibitory regulatory factors is partly responsible for the noted increase in collagen production and deposition in bleomycin-induced pulmonary fibrosis.

摘要

气管内给予博来霉素会导致肺纤维化,其特征为胶原蛋白合成和沉积增加。用来自正常大鼠和博来霉素处理大鼠的肺的中性盐可溶性提取物孵育正常肺碎块,会导致胶原蛋白和非胶原蛋白合成呈剂量依赖性抑制。然而,与正常肺提取物相比,博来霉素处理的肺提取物在这种抑制作用方面明显效果较差。这种抑制活性在标称分子量截留值为10,000的透析管中透析后并未减弱,但会被加热(70℃)和胰蛋白酶消化破坏。这种抑制活性不能归因于肺提取物中残留的血清或博来霉素。在Sephacryl S - 200(Pharmacia,皮斯卡塔韦,新泽西州)上进行分级分离显示,抑制活性具有异质性,其表观分子量大于100,000。脾脏提取物显示出类似的抑制活性,但正常脾脏和博来霉素处理的脾脏之间在强度上没有差异。这些数据表明,肺抑制调节因子产生的丧失或减少部分导致了博来霉素诱导的肺纤维化中胶原蛋白产生和沉积的显著增加。

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