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假孕期间小鼠子宫中前列腺素E受体亚型信使核糖核酸的“不同细胞定位”

'Distinct cellular localization' of the messenger ribonucleic acid for prostaglandin E receptor subtypes in the mouse uterus during pseudopregnancy.

作者信息

Katsuyama M, Sugimoto Y, Morimoto K, Hasumoto K, Fukumoto M, Negishi M, Ichikawa A

机构信息

Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.

出版信息

Endocrinology. 1997 Jan;138(1):344-50. doi: 10.1210/endo.138.1.4885.

Abstract

As an initial step to clarify the mechanisms of various uterine actions of PGE2, expression patterns of the messenger RNAs (mRNAs) for four subtypes of PGE receptors, EP1, EP2, EP3, and EP4, were investigated in the mouse uterus during pseudopregnancy. Relative expression levels were investigated by Northern blot analysis of mRNA levels in uteri obtained on days 0, 1, 3, 5, 7, and 9 of pseudopregnancy (day 0 = 48 h after PMSG injection), and cellular localization was determined by in situ hybridization in uteri obtained on days 0 and 5. EP2 mRNA was specifically expressed on day 5, and its expression was confined to the luminal epithelium. On the other hand, the level of the EP3 mRNA expression progressively increased until day 5. Cell populations expressing the EP3 mRNA were confined to the longitudinal smooth muscle on day 0, but they changed to the circular smooth muscle on day 5. The expression level of EP4 mRNA was low on days 0 and 1, but it became high on days 3 and 5. On day 0, EP4 mRNA was localized to the luminal epithelium. On day 5, diffuse, but significant, EP4 expression was observed over the endometrial stroma and epithelium. No EP1 mRNA signals were observed. Transient expression of EP2 on day 5 of pseudopregnancy in the luminal epithelium suggests its involvement in blastocyst implantation signaling. EP4 in the endometrial stroma is suggested to be involved in decidual transformation of the stromal cells, whereas EP3 in the myometrium is believed to be involved in regulation of myometrial activity.

摘要

作为阐明前列腺素E2(PGE2)各种子宫作用机制的第一步,研究了假孕期间小鼠子宫中前列腺素E受体四种亚型(EP1、EP2、EP3和EP4)的信使核糖核酸(mRNA)表达模式。通过对假孕第0、1、3、5、7和9天(第0天 = 注射孕马血清促性腺激素(PMSG)后48小时)获得的子宫mRNA水平进行Northern印迹分析来研究相对表达水平,并通过对第0天和第5天获得的子宫进行原位杂交来确定细胞定位。EP2 mRNA在第5天特异性表达,其表达局限于腔上皮。另一方面,EP3 mRNA表达水平在第5天之前逐渐升高。表达EP3 mRNA的细胞群体在第0天局限于纵行平滑肌,但在第5天变为环行平滑肌。EP4 mRNA的表达水平在第0天和第1天较低,但在第3天和第5天升高。在第0天,EP4 mRNA定位于腔上皮。在第5天,在内膜基质和上皮中观察到弥漫但显著的EP4表达。未观察到EP1 mRNA信号。假孕第5天腔上皮中EP2的瞬时表达表明其参与胚泡着床信号传导。子宫内膜基质中的EP4被认为参与基质细胞的蜕膜化转变,而子宫肌层中的EP3被认为参与子宫肌层活性的调节。

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