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子宫内膜中的胰岛素样生长因子及胰岛素样生长因子结合蛋白。宫内左炔诺孕酮释放的影响。

Insulin-like growth factors and insulin-like growth factor binding proteins in the endometrium. Effect of intrauterine levonorgestrel delivery.

作者信息

Rutanen E M

机构信息

Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Finland.

出版信息

Hum Reprod. 2000 Aug;15 Suppl 3:173-81. doi: 10.1093/humrep/15.suppl_3.173.

Abstract

Insulin-like growth factor (IGF) system is one of the growth factor systems that are believed to modulate steroid hormone actions in the endometrium through autocrine/paracrine mechanisms. IGF-I and IGF-II stimulate proliferation and differentiation, and maintain differentiated cell functions in several cell types in vitro. Endometrial stromal cells produce IGF-I and IGF-II as well as the high affinity IGF-binding proteins (IGFBP), whereas epithelial cells and, in a lesser amount, stromal cells contain cell membrane receptors for IGF. Oestrogen stimulates IGF-I gene expression, and IGF-II gene expression is associated with endometrial differentiation. The mRNA of six high affinity IGFBPs, which can modulate IGF actions, are expressed in human endometrium. The most abundant IGFBP in human endometrium is IGFBP-1, which is secreted by predecidualized/decidualized endometrial stromal cells in late secretory phase and during pregnancy. The primary negative regulator of IGFBP-1 production is insulin. IGFBP-1 competes with type I IGF receptor for binding of IGF in the endometrium and in cultured human trophoblastic cells. IGF-I mRNA is suppressed and mRNA encoding IGF-II and IGFBP-1 are consistently up-regulated in decidualized endometrium in women treated with the intrauterine levonorgestrel system (LNG-IUS). Strong cytoplasmic staining for IGFBP-1 was detected in decidualized endometrium in women using LNG-IUS for contraception or for endometrial protection during post-menopausal oestrogen replacement therapy. Simultaneously, oestrogen receptors were present, while progesterone receptors were hardly detectable in the endometrium by immunohistochemistry. The latter findings suggest that suppression of IGF-I action by IGFBP-1 may be one of the molecular mechanisms accounting for progestagenic and anti-oestrogenic effects of LNG-IUS in the endometrium. Consequently, examination of local IGF-I, IGF-II and IGFBP-1 expression might provide additional information when evaluating the effect of different progestins on the endometrium at the molecular level.

摘要

胰岛素样生长因子(IGF)系统是一种生长因子系统,人们认为它通过自分泌/旁分泌机制调节子宫内膜中的甾体激素作用。IGF-I和IGF-II可刺激增殖和分化,并在体外维持多种细胞类型的分化细胞功能。子宫内膜基质细胞可产生IGF-I、IGF-II以及高亲和力胰岛素样生长因子结合蛋白(IGFBP),而上皮细胞以及少量的基质细胞含有IGF的细胞膜受体。雌激素可刺激IGF-I基因表达,IGF-II基因表达与子宫内膜分化相关。六种可调节IGF作用的高亲和力IGFBP的mRNA在人子宫内膜中表达。人子宫内膜中最丰富的IGFBP是IGFBP-1,它由分泌晚期和孕期的前蜕膜化/蜕膜化子宫内膜基质细胞分泌。IGFBP-1产生的主要负调节因子是胰岛素。IGFBP-1在子宫内膜和培养的人滋养层细胞中与I型IGF受体竞争IGF的结合。在用宫内左炔诺孕酮系统(LNG-IUS)治疗的女性的蜕膜化子宫内膜中,IGF-I mRNA受到抑制,而编码IGF-II和IGFBP-1的mRNA持续上调。在使用LNG-IUS进行避孕或绝经后雌激素替代治疗期间用于子宫内膜保护的女性的蜕膜化子宫内膜中,检测到IGFBP-1有强烈的细胞质染色。同时,存在雌激素受体,而通过免疫组织化学在子宫内膜中几乎检测不到孕激素受体。后一项发现表明,IGFBP-1对IGF-I作用的抑制可能是LNG-IUS在子宫内膜中产生孕激素和抗雌激素作用的分子机制之一。因此,在分子水平评估不同孕激素对子宫内膜的影响时,检测局部IGF-I、IGF-II和IGFBP-1的表达可能会提供更多信息。

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