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首页> 外文期刊>Reproduction: The official journal of the Society for the Study of Fertility >The expression of fibroblast growth factor receptors during early bovine conceptus development and pharmacological analysis of their actions on trophoblast growth in vitro
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The expression of fibroblast growth factor receptors during early bovine conceptus development and pharmacological analysis of their actions on trophoblast growth in vitro

机译:成纤维细胞生长因子受体在牛早期子宫发育过程中的表达及其对体外滋养细胞生长作用的药理分析

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The overall aim of this work was to examine the expression profiles for fibroblast growth factor receptors (FGFRs) and describe their biological importance during bovine pre- and peri-implantation conceptus development. FGFR1 and FGFR2 mRNAs were detected at 1-, 2-, 8-cell, morula and blastocyst stages whereas FGFR3 and FGFR4 mRNAs were detected after the 8-cell stage but not earlier. The abundance of FGFR1 , FGFR3 , and FGFR4 mRNAs increased at the morula and blastocyst stages. Immunofluorescence microscopy detected FGFR2 and FGFR4 exclusively in trophoblast cells whereas FGFR1 and FGFR3 were detected in both trophoblast cells and inner cell mass in blastocysts. Neither transcripts for FGF10 nor its receptor ( FGFR2b ) were temporally related to interferon τ ( IFNT ) transcript profile during peri- and postimplantation bovine conceptus development. A series of studies used a chemical inhibitor of FGFR kinase function (PD173074) to examine FGFR activation requirements during bovine embryo development. Exposing embryos to the inhibitor (1?μM) beginning on day 5 post-fertilization did not alter the percentage of embryos that developed into blastocysts or blastocyst cell numbers. The inhibitor did not alter the abundance of CDX2 mRNA but decreased ( P <0.05) the relative abundance of IFNT mRNA in blastocysts. Exposing blastocysts to the inhibitor from days 8 to 11 post-fertilization reduced ( P <0.05) the percentage of blastocysts that formed outgrowths after transfer to Matrigel-coated plates. In conclusion, each FGFR was detected in bovine embryos, and FGFR activation is needed to maximize IFNT expression and permit outgrowth formation.
机译:这项工作的总体目标是检查成纤维细胞生长因子受体(FGFRs)的表达谱,并描述其在牛植入前和植入前后概念发展过程中的生物学重要性。在1、2、8,桑ula和胚泡阶段检测到FGFR1和FGFR2 mRNA,而在8细胞阶段之后但未更早检测到FGFR3和FGFR4 mRNA。在桑ula和胚泡阶段,FGFR1,FGFR3和FGFR4 mRNA的丰度增加。免疫荧光显微镜仅在滋养细胞中检测到FGFR2和FGFR4,而在滋养细胞和囊胚内部细胞中均检测到FGFR1和FGFR3。 FGF10及其受体(FGFR2b)的转录本在植入后和植入后牛概念发育过程中均与干扰素τ(IFNT)转录本在时间上无关。一系列研究使用了FGFR激酶功能的化学抑制剂(PD173074)来检查牛胚胎发育过程中FGFR的激活要求。受精后第5天开始将胚胎暴露于抑制剂(1?μM),不会改变发育为胚泡或胚泡细胞数目的胚的百分比。该抑制剂不会改变CDX2 mRNA的丰度,但会降低(P <0.05)囊胚中IFNτmRNA的相对丰度。受精后第8天至第11天将胚泡暴露于抑制剂可降低(P <0.05)胚泡转移至基质胶包被的平板后形成的胚泡百分比。总之,在牛胚胎中检测到每种FGFR,并且需要FGFR激活以最大化IFNτ表达并允许长出突起。

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