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库普弗细胞中部分特性因子增强大鼠肝细胞α2-巨球蛋白的分泌。

Alpha 2-macroglobulin secretion enhanced in rat hepatocytes by partially characterized factor from Kupffer cells.

作者信息

Hirata Y, Ishibashi H, Kimura H, Hayashida K, Nagano M, Okubo H

出版信息

Inflammation. 1985 Jun;9(2):201-9. doi: 10.1007/BF00917592.

Abstract

Isolated rat Kupffer cells produced a factor which stimulated the synthesis of alpha 2-macroglobulin (alpha 2M) in primary cultured rat hepatocytes. Although Kupffer cells placed in culture produced the factor without stimulation by lipopolysaccharide (LPS), the LPS-stimulated cells produced larger amounts of the factor. On the other hand, the production of the factor was inhibited by addition of actinomycin D. The induction of alpha 2M synthesis by cultured hepatocytes was enhanced in the presence of dexamethasone (Dex), in that hepatic synthesis of alpha 2M increased by addition of the factor alone and with Dex 1.5 and three- to four-fold, respectively. The factor was nondialyzable and stable at 60 degrees C for 30 min. When the factor was fractionated using the molecular sieve method, the activity recovered in the fraction had a molecular weight of over 30,000.

摘要

分离的大鼠库普弗细胞产生一种因子,该因子可刺激原代培养的大鼠肝细胞中α2-巨球蛋白(α2M)的合成。虽然培养的库普弗细胞在无脂多糖(LPS)刺激的情况下也能产生该因子,但经LPS刺激的细胞产生的该因子量更多。另一方面,放线菌素D的添加会抑制该因子的产生。在地塞米松(Dex)存在的情况下,培养的肝细胞对α2M合成的诱导作用增强,即单独添加该因子时肝α2M合成增加,同时添加该因子和Dex时,肝α2M合成分别增加1.5倍以及三到四倍。该因子不能透过透析膜,在60℃下30分钟内稳定。当使用分子筛方法对该因子进行分级分离时,在该级分中恢复的活性物质分子量超过30,000。

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