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首页> 外文期刊>Molecular reproduction and development >Expression of fibroblast growth factor 10 and its receptor, fibroblast growth factor receptor 2B, in the bovine corpus luteum.
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Expression of fibroblast growth factor 10 and its receptor, fibroblast growth factor receptor 2B, in the bovine corpus luteum.

机译:成纤维细胞生长因子10及其受体,成纤维细胞生长因子受体2B在黄体中的表达。

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摘要

There is evidence that several fibroblast growth factors (FGFs) are involved in growth and development of the corpus luteum (CL), but many FGFs have not been investigated in this tissue, including FGF10. The objective of this study was to determine if FGF10 and its receptor (FGFR2B) are expressed in the CL. Bovine CL were collected from an abattoir and classed as corpus hemorrhagica (stage I), developing (stage II), developed (stage III), and regressed (stage IV) CL. Expression of FGF10 and FGFR2B mRNA was measured by reverse transcription-polymerase chain reaction (RT-PCR). Both genes were expressed in bovine CL, and FGF10 expression did not differ between stages of CL development. FGF10 protein was localized to large and small luteal cells by immunohistochemistry. FGFR2B expression was approximately threefold higher in regressed compared to developing and developed CL (P < 0.05). To determine if FGF10 and FGFR2B expression is regulated during functional luteolysis, cattle were injected with PGF2alphaand CL collected at 0, 0.5, 2, 4, 12, 24, 48, and 64 hr thereafter (n = 5 CL/time point), and mRNA abundance was measured by real-time RT-PCR. FGF10 mRNA expression did not change during functional luteolysis, whereas FGFR2B mRNA abundance decreased significantly at 2, 4, and 12 hr after PGF2alpha, and returned to pretreatment levels for the period 24-64 hr post-PGF2alpha. These data suggest a potential role for FGFR2B signaling during structural luteolysis in bovine CL.
机译:有证据表明几种成纤维细胞生长因子(FGF)参与了黄体(CL)的生长和发育,但是尚未在该组织中研究许多FGF,包括FGF10。这项研究的目的是确定FGF10及其受体(FGFR2B)是否在CL中表达。从屠宰场收集牛CL,并将其分类为出血性(体(I期),发育中(II期),发育中(III期)和退化(IV期)。通过逆转录-聚合酶链反应(RT-PCR)测量FGF10和FGFR2B mRNA的表达。两种基因均在牛CL中表达,并且在CL发育的各个阶段之间FGF10的表达没有差异。 FGF10蛋白通过免疫组织化学定位于大,小黄体细胞。与发育和发育中的CL相比,FGFR2B表达的回归约高三倍(P <0.05)。为了确定功能性黄体溶解期间FGF10和FGFR2B的表达是否受到调节,向牛注射了PGF2alpha和CL,分别在0、0.5、2、4、12、24、48和64小时(n = 5 CL /时间点)采集,通过实时RT-PCR测量mRNA丰度。在功能性黄体溶解期间,FGF10 mRNA的表达没有改变,而在PGF2alpha之后的2、4和12小时,FGFR2B mRNA的丰度显着降低,并在PGF2alpha之后的24-64小时恢复到预处理水平。这些数据表明在牛CL结构性黄体溶解过程中FGFR2B信号的潜在作用。

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