首页> 美国卫生研究院文献>The Journal of Reproduction and Development >Expression and localization of members of the thrombospondin family during final follicle maturation and corpus luteum formation and function inthe bovine ovary
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Expression and localization of members of the thrombospondin family during final follicle maturation and corpus luteum formation and function inthe bovine ovary

机译:最终卵泡成熟和黄体形成和功能中血小板反应蛋白家族成员的表达和定位。牛卵巢

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摘要

The aim of this study was to characterize the expression patterns and localization of the thrombospondin family members (THBS1, THBS2) and their receptors (CD36 and CD47) in bovine ovaries. First, the antral follicles were classified into 5 groups based on the follicle size and estradiol-17beta (E2) concentration in the follicular fluid (< 0.5, 0.5–5, 5–40, 40–180 and >180 E2 ng/ml). Second, the corpus luteum (CL) was assigned to the following stages: days 1–2, 3–4, 5–7, 8–12, 13–16 and >18 of the estrous cycle and of pregnancy (month 1–2, 3–4, 6–7 and > 8). Third, the corpora lutea were collected by transvaginal ovariectomy before and 0.5, 2, 4, 12, 24, 48 and 64 h after inducing luteolysis by injecting a prostaglandin F2alpha analog. The mRNA expression of examined factors was measured by RT-qPCR, steroid hormone concentration by EIA, and localization by immunohistochemistry. The mRNA expression of THBS1, THBS2, CD36, and CD47 in the granulosa cells and theca interna was high in the small follicles and reduced in the preovulatory follicles. The mRNA expression of THBS1, THBS2, and CD47 in the CL during the estrous cycle was high, but decreased significantly during pregnancy. After induced luteolysis, thrombospondins increased significantly to reach the maximum level at 12 h for THBS1, 24 h for THBS2, and 48 h for CD36. The temporal expression and localization pattern of the thrombospondins and their specific receptors in the antral follicles and corpora lutea during the different physiological phases of the estrous cycle and induced luteolysis appear to be compatible with their inhibitory role in the control of ovarian angiogenesis.
机译:这项研究的目的是表征血小板反应蛋白家族成员(THBS1,THBS2)及其受体(CD36和CD47)在牛卵巢中的表达模式和定位。首先,根据卵泡大小和卵泡液中雌二醇-17β(E2)的浓度(<0.5、0.5–5、5–40、40–180和> 180 E2 ng / ml)将肛门卵泡分为5组。 。其次,将黄体(CL)分为以下阶段:发情周期和怀孕(1-2个月)的1-2、3-4、5-7、8-12、13-16和> 18天,3-4、6-7和> 8)。第三,在通过注射前列腺素F2α类似物诱导黄体溶解之前和之后0.5、2、4、12、24、48和64小时,通过经阴道卵巢切除术收集黄体。通过RT-qPCR测量所检查因子的mRNA表达,通过EIA测量类固醇激素浓度,并通过免疫组织化学测量定位。 THBS1,THBS2,CD36和CD47在颗粒细胞和鞘膜中的mRNA表达在小卵泡中较高,而在排卵前卵泡中则降低。在动情周期中,CL中THBS1,THBS2和CD47的mRNA表达较高,但在怀孕期间明显降低。诱导黄体溶解后,血小板反应蛋白显着增加,THBS1在12 h,THBS2在24 h,CD36在48 h达到最大水平。在动情周期的不同生理阶段和诱导的黄体溶解期间,血小板反应蛋白及其特定受体在窦房滤泡和黄体中的时间表达和定位模式似乎与它们在控制卵巢血管生成中的抑制作用兼容。

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