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卵巢淋巴管的发生和激素调节。

Development and hormonal regulation of the ovarian lymphatic vasculature.

机构信息

School of Pediatrics and Reproductive Health, Robinson Institute, University of Adelaide, Adelaide, South Australia, Australia.

出版信息

Endocrinology. 2010 Nov;151(11):5446-55. doi: 10.1210/en.2010-0629. Epub 2010 Sep 15.

Abstract

The lymphatic vasculature plays a number of essential physiological roles including maintaining fluid homeostasis, providing a network for the transport of immune cells, and facilitating the uptake of fat-soluble nutrients from the gastrointestinal tract. Although the critical importance and remodeling capacity of the blood vasculature has been well described within the ovary, just a few reports describe the lymphatic vasculature. Using histological and molecular techniques, we report the kinetics of ovarian lymphangiogenesis and the hormonal regulation of lymphangiogenic growth factors associated with key stages of ovarian follicle growth. We exploited the Adamts1-null mouse model, a model with a previously characterized lymphatic defect to further interrogate the mechanisms controlling ovarian lymphangiogenesis. The establishment and development of the ovarian lymphatic vascular network in postnatal developing ovaries was associated with the presence and hormonal regulation of the lymphangiogenic growth factors and their receptors, including Vegfc, Vegfd, and Vegfr3. We characterized the hormonally regulated remodeling of the ovarian lymphatic vasculature in response to FSH and estradiol. The lymphatic network was defective in the Adamts1-null ovary, clearly demonstrating both the involvement of FSH/estradiol and the Adamts1 (a disintegrin and metalloproteinase with thrombospondin motifs 1) protease in ovarian lymphangiogenesis. This study provides the first evidence of a malleable lymphatic system responsive to hormonal changes of the female reproductive cycle, at least in the mouse ovary, suggesting a role for lymphatic vessel functions in normal folliculogenesis.

摘要

淋巴管系统发挥着许多重要的生理作用,包括维持液体平衡、为免疫细胞的运输提供网络,并促进胃肠道中脂溶性营养素的吸收。尽管血液脉管系统的重要性和重塑能力在卵巢中已经得到了很好的描述,但只有少数报道描述了淋巴管系统。本研究使用组织学和分子技术,报告了卵巢淋巴管生成的动力学以及与卵巢卵泡生长关键阶段相关的淋巴管生成生长因子的激素调节。我们利用了 Adamts1 基因敲除小鼠模型,该模型具有先前表征的淋巴管缺陷,以进一步探究控制卵巢淋巴管生成的机制。在产后发育的卵巢中,卵巢淋巴管网络的建立和发育与淋巴管生成生长因子及其受体的存在和激素调节有关,包括 Vegfc、Vegfd 和 Vegfr3。我们描述了卵巢淋巴管对 FSH 和雌二醇的激素调节重塑。Adamts1 基因敲除卵巢中的淋巴管网络存在缺陷,这清楚地表明 FSH/雌二醇和 Adamts1(一种具有血小板反应蛋白基序的解整合素和金属蛋白酶 1)蛋白酶都参与了卵巢淋巴管生成。这项研究首次提供了证据,表明女性生殖周期的激素变化会导致可塑的淋巴管系统发生变化,至少在小鼠卵巢中是如此,这表明淋巴管功能在正常卵泡发生中起作用。

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