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组胺诱导抑制因子(HSF):对迁移抑制因子(MIF)产生及增殖的影响

Histamine-induced suppressor factor (HSF): effect on migration inhibitory factor (MIF) production and proliferation.

作者信息

Rocklin R E

出版信息

J Immunol. 1977 May;118(5):1734-8.

PMID:67146
Abstract

Histamine added in vitro to cultures of sensitized lymphocytes suppresses antigen-induced production of migration inhibitory factor (MIF) and proliferation by these cells. Recent studies have suggested that lymphocytes bearing histamine type-2 receptors play a regulatory role in these in vitro responses. The present studies were undertaken to determine if suppressor function by cells having histamine receptors was mediated through a soluble product. It was found that lymph node cells from nonimmune or immune strain 2 guinea pigs elaborate a nondialyzable factor into the culture supernatant when incubated with 10(-3) to 10(-5) M histamine (histamine-induced suppressor factor of HSF). HSF, when cocultured with sensitized lymphocytes, suppressed their MIF and proliferative responses to antigen. HSF was made by lymphocytes but not macrophages. Its production could be blocked by an H2 receptor antagonist (burimamide) but not an H1 receptor antagonist (chlorpheniramine). Furthermore, the inhibitory effect of HSF was reversible as lymphocytes washed free of the factor after 24 hr and recultured with fresh medium and antigen were able to produce MIF. Gel filtration by Sephadex G-100 chromatography indicated that HSF had an approximate m.w. of 23,000 to 40,000. These results suggest that the release of histamine at the sites of immediate hypersensitivity reactions, possibly by generating HSF activity, may play a regulatory role in the subsequent development of cellular-immune reactions at the same site.

摘要

体外向致敏淋巴细胞培养物中添加组胺可抑制这些细胞抗原诱导的迁移抑制因子(MIF)产生及增殖。最近的研究表明,带有组胺2型受体的淋巴细胞在这些体外反应中起调节作用。本研究旨在确定具有组胺受体的细胞的抑制功能是否通过一种可溶性产物介导。发现来自非免疫或免疫2系豚鼠的淋巴结细胞在与10⁻³至10⁻⁵M组胺孵育时,会向培养上清液中分泌一种不可透析的因子(组胺诱导的抑制因子,HSF)。HSF与致敏淋巴细胞共培养时,会抑制它们对抗原的MIF和增殖反应。HSF由淋巴细胞而非巨噬细胞产生。其产生可被H₂受体拮抗剂(布立马胺)阻断,但不能被H₁受体拮抗剂(氯苯那敏)阻断。此外,HSF的抑制作用是可逆的,因为24小时后洗去该因子并重新用新鲜培养基和抗原培养的淋巴细胞能够产生MIF。通过Sephadex G - 100柱层析进行凝胶过滤表明,HSF的分子量约为23,000至40,000。这些结果表明,在速发型超敏反应部位组胺的释放,可能通过产生HSF活性,在同一部位随后的细胞免疫反应发展中起调节作用。

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