首页> 外文期刊>AJRI: American Journal of Reproductive Immunology >Progesterone induced blocking factor (PIBF) mediates progesterone induced suppression of decidual lymphocyte cytotoxicity.
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Progesterone induced blocking factor (PIBF) mediates progesterone induced suppression of decidual lymphocyte cytotoxicity.

机译:孕激素诱导的阻断因子(PIBF)介导孕激素诱导的蜕膜蜕膜细胞毒性抑制。

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PROBLEM: Progesterone induced blocking factor (PIBF) is a mediator of progesterone that blocks peripheral blood lytic natural killer (NK) activity. Progesterone or PIBF stimulated decidual macrophages block up-regulation of perforin expression in decidual lymphocytes (DL). Therefore, we investigated whether progesterone regulates cytotoxicity of DL. METHOD OD STUDY: Decidual mononuclear cells were cultured with progesterone. PIBF, progesterone and anti-PIBF antibody or in the medium only. Cytolytic activity of non-adherent DL was measured by PKH-26 (red) 2 hr cytolytic assay and flow cytometry. Perforin positive DL were detected by immunofluorescency and PIBF-positive cells by immunohistology. RESULTS: Progesterone and PIBF, in a dose-dependent manner decreased cytotoxicity of DL against K-562 targets, and perforin egzocytosys was blocked. Anti-PIBF antibodies reversed the progesterone mediated reduction in cytolytic activity of DL. PIBF positive cells were found in first trimester pregnancy decidua. CONCLUSION: The results indicate possible role for PIBF, as a mediator of progesterone in regulation of DL cytolytic activity at the maternal-foetal (M-F) interface.
机译:问题:孕激素诱导的阻断因子(PIBF)是孕激素的介体,可阻断外周血溶解性自然杀伤(NK)活性。孕酮或PIBF刺激的蜕膜巨噬细胞阻止了蜕膜淋巴细胞(DL)中穿孔素表达的上调。因此,我们调查了孕激素是否调节DL的细胞毒性。方法OD研究:用孕酮培养蜕膜单个核细胞。 PIBF,孕酮和抗PIBF抗体或仅在培养基中。通过PKH-26(红色)2小时细胞溶解测定法和流式细胞仪测量非粘附性DL的细胞溶解活性。免疫荧光检测穿孔素阳性DL,免疫组织学检测PIBF阳性细胞。结果:孕酮和PIBF以剂量依赖性方式降低了DL对K-562靶标的细胞毒性,并阻断了穿孔素egzocytosys。抗PIBF抗体逆转了孕激素介导的DL细胞溶解活性的降低。在妊娠早期的蜕膜中发现了PIBF阳性细胞。结论:结果表明PIBF作为孕激素的介体可能在母体-胎儿(M-F)界面调节DL细胞溶解活性中发挥作用。

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