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巨噬细胞炎性蛋白-3β在人子宫内膜整个月经周期中的表达

Expression of macrophage inflammatory protein-3beta in human endometrium throughout the menstrual cycle.

作者信息

Daikoku Nobue, Kitaya Kotaro, Nakayama Takeshi, Fushiki Shinji, Honjo Hideo

机构信息

Department of Obstetrics and Gynecology, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kamigyo-ku, Kyoto, Japan 602-8566.

出版信息

Fertil Steril. 2004 Mar;81 Suppl 1:876-81. doi: 10.1016/j.fertnstert.2003.09.036.

Abstract

OBJECTIVE

To determine the expression of macrophage inhibitory protein-3beta (MIP-3beta), a potential chemoattractant for endometrial natural killer (NK) cells, in the human endometrium.

DESIGN

An experimental study.

SETTING

University department of obstetrics and gynecology.

PATIENT(S): Thirty-seven fertile women with regular menstrual cycles and nonpathological endometrium, undergoing hysterectomy.

INTERVENTION(S): Endometrium was obtained from operative samples.

MAIN OUTCOME MEASURE(S): Paraffin-embedded endometrium was immunostained to determine the localization of MIP-3beta. The number of NK cells was counted in 10 nonoverlapping stromal areas. The MIP-3beta concentration in the homogenized endometrium was determined by ELISA.

RESULT(S): Immunoreactivity for MIP-3beta was observed in the surface epithelia, glandular epithelia, and stroma with some menstrual cycle-dependent fluctuation. The MIP-3beta concentration was significantly higher in the late secretory phase than in the other phases. It showed a trend toward correlation with the number of endometrial NK cells.

CONCLUSION(S): MIP-3beta was expressed in the human endometrium, but our results could not strongly support the hypothesis that MIP-3beta is a potential chemoattractant for endometrial NK cells.

摘要

目的

确定巨噬细胞抑制蛋白-3β(MIP-3β)在人子宫内膜中的表达,MIP-3β是子宫内膜自然杀伤(NK)细胞的一种潜在趋化因子。

设计

一项实验研究。

地点

大学妇产科系。

患者

37名月经周期规律且子宫内膜无病变的育龄妇女,接受子宫切除术。

干预措施

从手术样本中获取子宫内膜。

主要观察指标

对石蜡包埋的子宫内膜进行免疫染色以确定MIP-3β的定位。在10个不重叠的基质区域中计数NK细胞的数量。通过酶联免疫吸附测定法(ELISA)测定匀浆子宫内膜中MIP-3β的浓度。

结果

在表面上皮、腺上皮和基质中观察到MIP-3β的免疫反应性,且有一些月经周期依赖性波动。分泌晚期MIP-3β浓度显著高于其他时期。它与子宫内膜NK细胞数量呈相关趋势。

结论

MIP-3β在人子宫内膜中表达,但我们的结果不能有力支持MIP-3β是子宫内膜NK细胞潜在趋化因子这一假说。

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