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子宫内膜异位症的触珠蛋白与腹膜巨噬细胞结合,并改变子宫内膜异位症女性患者巨噬细胞的功能。

Endometriotic haptoglobin binds to peritoneal macrophages and alters their function in women with endometriosis.

作者信息

Sharpe-Timms Kathy L, Zimmer Randy L, Ricke Emily A, Piva Marta, Horowitz Gary M

机构信息

Department of Obstetrics and Gynecology, University of Missouri-Columbia, Columbia, Missouri 65212, USA.

出版信息

Fertil Steril. 2002 Oct;78(4):810-9. doi: 10.1016/s0015-0282(02)03317-4.

Abstract

OBJECTIVE

To evaluate the effects of endometriotic haptoglobin on peritoneal macrophage function.

DESIGN

Prospective laboratory study.

SETTING

School of medicine.

PATIENT(S): Twenty-three women with and without endometriosis.

INTERVENTION(S): Peritoneal macrophages cultured without or with haptoglobin.

MAIN OUTCOME MEASURE(S): Peritoneal macrophage haptoglobin immunoreactivity, adhesion, and interleukin-6 (IL-6) production.

RESULT(S): In vivo, significantly more peritoneal macrophages from women with endometriosis bound haptoglobin and exhibited reduced adhesion compared to women without endometriosis. In vitro, haptoglobin treatment significantly decreased peritoneal macrophage adherence only in women without endometriosis; this effect was not seen in women with endometriosis, probably owing to in vivo haptoglobin saturation. Conversely, haptoglobin treatment robustly increased IL-6 production only by macrophages from women with endometriosis, suggesting differential immune response in these women.

CONCLUSION(S): Endometriotic lesions synthesize and secrete a unique form of haptoglobin (endometriosis protein-I) that is up-regulated by IL-6. This study shows that haptoglobin adheres to peritoneal macrophages; decreases adhesion, which may influence phagocytic function; and up-regulates IL-6 production. Hence, a feed-forward loop is proposed whereby endometriotic lesion haptoglobin decreases macrophage phagocytic function while increasing IL-6 production, which in turn increases endometriotic haptoglobin and promotes establishment of endometriosis.

摘要

目的

评估子宫内膜异位症患者的触珠蛋白对腹膜巨噬细胞功能的影响。

设计

前瞻性实验室研究。

地点

医学院。

患者

23名患有和未患有子宫内膜异位症的女性。

干预措施

在有或无触珠蛋白的情况下培养腹膜巨噬细胞。

主要观察指标

腹膜巨噬细胞触珠蛋白免疫反应性、黏附能力及白细胞介素-6(IL-6)的产生。

结果

在体内,与未患子宫内膜异位症的女性相比,患有子宫内膜异位症的女性腹膜巨噬细胞结合触珠蛋白的数量显著更多,且黏附能力降低。在体外,触珠蛋白处理仅在未患子宫内膜异位症的女性中显著降低了腹膜巨噬细胞的黏附;而在患有子宫内膜异位症的女性中未观察到这种效果,可能是由于体内触珠蛋白饱和。相反,触珠蛋白处理仅显著增加了患有子宫内膜异位症女性巨噬细胞的IL-6产生,表明这些女性存在不同的免疫反应。

结论

子宫内膜异位症病灶合成并分泌一种独特形式的触珠蛋白(子宫内膜异位症蛋白-I),其受IL-6上调。本研究表明,触珠蛋白可黏附于腹膜巨噬细胞;降低黏附能力,这可能影响吞噬功能;并上调IL-6的产生。因此,提出了一个前馈回路,即子宫内膜异位症病灶触珠蛋白降低巨噬细胞吞噬功能,同时增加IL-6产生,进而增加子宫内膜异位症触珠蛋白并促进子宫内膜异位症的形成。

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