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用伴放线放线杆菌脂多糖刺激的P388D1小鼠巨噬细胞系产生白细胞介素-1抑制剂。

Production of an interleukin-1 inhibitor by cell line P388D1 murine macrophages stimulated with Haemophilus actinomycetemcomitans lipopolysaccharide.

作者信息

Nishihara T, Koga T, Hamada S

机构信息

Department of Dental Research, National Institute of Health, Tokyo, Japan.

出版信息

Infect Immun. 1988 Nov;56(11):2801-7. doi: 10.1128/iai.56.11.2801-2807.1988.

Abstract

Murine macrophages of the P388D1 cell line stimulated with lipopolysaccharide (LPS) from Haemophilus actinomycetemcomitans Y4 released an interleukin-1 (IL-1) inhibitor, as well as IL-1. Maximal IL-1 activity in culture supernatants was detected after 24 h of culture. On the other hand, IL-1 inhibitor activity reached a maximum level after 72 h of culture. An IL-1 inhibitor was partially purified from the culture supernatant of P388D1 cells stimulated with Y4 LPS for 72 h by ammonium sulfate precipitation, followed by Sephacryl S-200 gel chromatography. A 160-kilodalton peak inhibitory to IL-1 and a 14-kilodalton peak showing IL-1 activity were separated by Sephacryl S-200 column chromatography. The partially purified IL-1 inhibitor significantly suppressed the proliferation of C3H/HeJ murine thymocytes that had been induced with murine and human IL-1 in the presence of a submitogenic dose of concanavalin A. The IL-1 inhibitor more strongly suppressed human recombinant IL-1 beta than human recombinant IL-1 alpha. This inhibitory activity of the partially purified preparation was unaffected by the presence of trypsin inhibitor and the protease inhibitor aprotinin. The IL-1 inhibitor did not exhibit either IL-2 or IL-2 inhibitor activity. The inhibitor suppressed C3H/HeJ thymocyte proliferation induced by IL-1 in the presence of a saturated concentration of IL-2 instead of a suboptimal concentration of concanavalin A. These results indicate that prolonged culture of Y4 LPS-stimulated murine macrophages releases a specific inhibitor of IL-1.

摘要

用放线共生放线杆菌Y4的脂多糖(LPS)刺激P388D1细胞系的小鼠巨噬细胞,可释放白细胞介素-1(IL-1)抑制剂以及IL-1。培养24小时后,在培养上清液中检测到最大IL-1活性。另一方面,IL-1抑制剂活性在培养72小时后达到最高水平。通过硫酸铵沉淀,随后进行Sephacryl S-200凝胶色谱法,从用Y4 LPS刺激72小时的P388D1细胞培养上清液中部分纯化出IL-1抑制剂。通过Sephacryl S-200柱色谱法分离出对IL-1有抑制作用的160千道尔顿峰和显示IL-1活性的14千道尔顿峰。部分纯化的IL-1抑制剂在亚致有丝分裂剂量的伴刀豆球蛋白A存在下,能显著抑制由小鼠和人IL-1诱导的C3H/HeJ小鼠胸腺细胞的增殖。该IL-1抑制剂对人重组IL-1β的抑制作用比对人重组IL-1α更强。部分纯化制剂的这种抑制活性不受胰蛋白酶抑制剂和蛋白酶抑制剂抑肽酶存在的影响。该IL-1抑制剂既不表现出IL-2活性也不表现出IL-2抑制剂活性。在存在饱和浓度的IL-2而非亚最佳浓度的伴刀豆球蛋白A的情况下,该抑制剂抑制了由IL-1诱导的C3H/HeJ胸腺细胞增殖。这些结果表明,用Y4 LPS刺激的小鼠巨噬细胞长时间培养会释放一种特异性的IL-1抑制剂。

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