VEGFR-1 blockade disrupts peri-implantation decidual angiogenesis and macrophage recruitment.

Q4 Neuroscience Vascular Cell Pub Date : 2014-08-01 eCollection Date: 2014-01-01 DOI:10.1186/2045-824X-6-16
Nataki C Douglas, Ralf C Zimmermann, Qian Kun Tan, Chantae S Sullivan-Pyke, Mark V Sauer, Jan K Kitajewski, Carrie J Shawber
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引用次数: 25

Abstract

Background: Angiogenesis and macrophage recruitment to the uterus are key features of uterine decidualization; the progesterone-mediated uterine changes that allow for embryo implantation and initiation of pregnancy. In the current study, we characterized the expression of vascular endothelial growth factor receptor-1 (VEGFR-1) in macrophages and endothelial cells of the peri-implantation uterus and determined if VEGFR-1 function is required for decidual angiogenesis, macrophage recruitment, and/or the establishment of pregnancy.

Methods: Expression of VEGFR-1 in uterine endothelial cells and macrophages was determined with immunohistochemistry. To assess the effect of continuous VEGFR-1 blockade, adult female mice were given VEGFR-1 blocking antibody, MF-1, every 3 days for 18 days. After 6 doses, females were mated and a final dose of MF-1 was given on embryonic day 3.5. Endothelial cells and macrophages were quantified on embryonic day 7.5. Pregnancy was analyzed on embryonic days 7.5 and 10.5.

Results: F4/80(+) macrophages are observed throughout the stroma and are abundant adjacent to the endometrial lumen and glands prior to embryo implantation and scatter throughout the decidua post implantation. VEGFR-1 expression is restricted to the uterine endothelial cells. F4/80(+) macrophages were often found adjacent to VEGFR-1(+) endothelial cells in the primary decidual zone. Continuous VEGFR-1 blockade correlates with a significant reduction in decidual vascular and macrophage density, but does not affect embryo implantation or maintenance of pregnancy up to embryonic day 10.5.

Conclusions: We found that VEGFR-1 functions in both decidual angiogenesis and macrophage recruitment to the implantation site during pregnancy. VEGFR-1 is expressed by endothelial cells, however blocking VEGFR-1 function in endothelial cells results in reduced macrophage recruitment to the uterus. VEGFR-1 blockade did not compromise the establishment and/or maintenance of pregnancy.

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VEGFR-1阻断破坏着床期蜕膜血管生成和巨噬细胞募集。
背景:血管生成和巨噬细胞向子宫募集是子宫去个体化的关键特征;黄体酮介导的子宫变化,使胚胎着床和怀孕开始。在目前的研究中,我们表征了血管内皮生长因子受体-1 (VEGFR-1)在巨噬细胞和着床周子宫内皮细胞中的表达,并确定了VEGFR-1的功能是否需要蜕膜血管生成、巨噬细胞募集和/或妊娠的建立。方法:采用免疫组化方法检测子宫内皮细胞和巨噬细胞中VEGFR-1的表达。为了评估持续阻断VEGFR-1的效果,成年雌性小鼠每3天给予VEGFR-1阻断抗体MF-1,持续18天。6次给药后,雌性进行交配,在胚胎第3.5天给药。胚胎第7.5天定量内皮细胞和巨噬细胞。在胚胎7.5天和10.5天分析妊娠情况。结果:F4/80(+)巨噬细胞遍布间质,胚胎着床前在子宫内膜腔和腺体附近大量存在,着床后分散在蜕膜中。VEGFR-1的表达仅限于子宫内皮细胞。F4/80(+)巨噬细胞常与原发性蜕膜区VEGFR-1(+)内皮细胞相邻。持续的VEGFR-1阻断与蜕膜血管和巨噬细胞密度的显著降低相关,但不影响胚胎着床或维持妊娠直至胚胎10.5天。结论:我们发现VEGFR-1在妊娠期蜕膜血管生成和巨噬细胞向着床部位募集中均有作用。VEGFR-1由内皮细胞表达,然而阻断内皮细胞中VEGFR-1的功能导致巨噬细胞向子宫募集减少。VEGFR-1阻断不影响妊娠的建立和/或维持。
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来源期刊
Vascular Cell
Vascular Cell Neuroscience-Neurology
CiteScore
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