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糖皮质激素对小鼠海绵肉芽肿及培养的肉芽肿成纤维细胞胶原蛋白合成的抑制作用。

Inhibitory effects of glucocorticoids on collagen synthesis by mouse sponge granulomas and granuloma fibroblasts in culture.

作者信息

Kruse N J, Rowe D W, Fujimoto W Y, Bornstein P

出版信息

Biochim Biophys Acta. 1978 Apr 19;540(1):101-16. doi: 10.1016/0304-4165(78)90439-7.

Abstract

The basis for the glucocorticoid-mediated decrease in tissue collagen was studied in mouse granulomas and in primary granuloma fibroblast cultures. Injection of mice for 12 days with dexamethasone (0.35 mg/kg body weight) resulted in a 50--70% inhibition of collagen synthesis and accumulation in polyvinyl sponge-induced granulomas whereas total protein synthesis was inhibited by only about 25%. The decreased collagen content of the granuloma was accounted for by both a reduced fibroblast number and diminished synthesis per cell. Growth rates, total protein synthesis and collagen synthesis were the same in granuloma fibroblast cultures derived from control or steroid-treated mice. However, addition of 3.10(-7) M hydrocortisone to the culture medium caused a 30--50% inhibition of both collagen and non-collagen protein synthesis in firbroblasts from either source. These inhibitory effects were dose- and time-dependent with a lag time of 12--24 h. Prolyl hydroxylase activity was reduced both in sponge granulomas from glucocorticoid-treated mice and in hydrocortisone-treated fibroblast cultures. However, protein synthesis was inhibited to the same extent as the inhibition of prolyl hydroxylase activity and there was no effect on peptidyl prolyl hydroxylation. These results indicate that the glucocorticoid-induced reduction of collagen synthesis and accumulation observed in mouse granulomas and primary granuloma fibroblast cultures is not specific for this protein. Furthermore, glucocorticoid-induced inhibition of collagen synthesis cannot be attributed to underhydroxylation of collagen prolyl residues.

摘要

在小鼠肉芽肿和原发性肉芽肿成纤维细胞培养物中研究了糖皮质激素介导的组织胶原蛋白减少的基础。给小鼠注射地塞米松(0.35mg/kg体重)12天,导致聚乙烯海绵诱导的肉芽肿中胶原蛋白合成和积累受到50%-70%的抑制,而总蛋白合成仅受到约25%的抑制。肉芽肿中胶原蛋白含量的降低是由于成纤维细胞数量减少和每个细胞合成减少所致。来自对照或类固醇处理小鼠的肉芽肿成纤维细胞培养物中的生长速率、总蛋白合成和胶原蛋白合成相同。然而,向培养基中添加3.10(-7)M氢化可的松会导致来自任何一种来源的成纤维细胞中胶原蛋白和非胶原蛋白合成受到30%-50%的抑制。这些抑制作用具有剂量和时间依赖性,滞后时间为12-24小时。糖皮质激素处理的小鼠的海绵肉芽肿和氢化可的松处理的成纤维细胞培养物中脯氨酰羟化酶活性均降低。然而,蛋白质合成受到的抑制程度与脯氨酰羟化酶活性的抑制程度相同,并且对肽基脯氨酰羟化没有影响。这些结果表明,在小鼠肉芽肿和原发性肉芽肿成纤维细胞培养物中观察到的糖皮质激素诱导的胶原蛋白合成和积累减少并非该蛋白质所特有的。此外,糖皮质激素诱导的胶原蛋白合成抑制不能归因于胶原蛋白脯氨酰残基的羟化不足。

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