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从小鼠和兔子的纯化多形核白细胞中产生淋巴细胞增殖增强因子。

Production of a lymphocyte proliferation potentiating factor by purified polymorphonuclear leucocytes from mice and rabbits.

作者信息

Goto F, Nakamura S, Goto K, Yoshinaga M

出版信息

Immunology. 1984 Dec;53(4):683-92.

Abstract

Highly pure polymorphonuclear leucocytes (PMN) were prepared from peritoneal exudate cells which were induced by an i.p. injection of casein into C3H mice and rabbits. The PMN were tested for the production of a lymphocyte proliferation potentiating factor with various stimulations in vitro. In both animal species, the purified PMN from the inflammatory site 3 hr after injection (3-hr PMN) produced the factor upon stimulation with kaolin, while the purified PMN from the lesion 24 hr after injection (24-hr PMN) did not. The 3-hr PMN produced the potentiating factor during a relatively earlier period after in vitro stimulation with kaolin. Protein synthesis inhibitors did not inhibit the factor production, suggesting the release of a preformed factor from 3-hr PMN. The effect of kaolin did not appear to be simply due to its cytotoxicity, because the release was dependent on the metabolism of 3-hr PMN and not parallel with 51Cr-release from the PMN. The factor produced by mouse PMN had an MW of about 15,000-25,000; it consisted of two isoelectrophoretically distinct factors, i.e. pI 9.4 and 5.4. The rabbit PMN factor was slightly smaller (MW ranging between 10,000 and 20,000) than the mouse PMN factor and was composed of three pI species, i.e. 7.2, 5.4, and 4.5.

摘要

通过向C3H小鼠和兔子腹腔注射酪蛋白诱导腹腔渗出细胞,从中制备出高度纯化的多形核白细胞(PMN)。对PMN进行体外各种刺激,检测其淋巴细胞增殖增强因子的产生情况。在这两种动物中,注射后3小时炎症部位的纯化PMN(3小时PMN)经高岭土刺激后产生该因子,而注射后24小时损伤部位的纯化PMN(24小时PMN)则不产生。3小时PMN在体外经高岭土刺激后相对较早的时期产生增强因子。蛋白质合成抑制剂不抑制该因子的产生,表明3小时PMN释放的是预先形成的因子。高岭土的作用似乎并非仅仅因其细胞毒性,因为这种释放依赖于3小时PMN的代谢,且与PMN的51Cr释放不平行。小鼠PMN产生的因子分子量约为15,000 - 25,000;它由两种等电点不同的因子组成,即pI 9.4和5.4。兔PMN因子比小鼠PMN因子略小(分子量在10,000至20,000之间),由三种pI成分组成,即7.2、5.4和4.5。

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