Suppr超能文献

瞬时受体电位通道在小鼠子宫内膜中的功能表达。

The functional expression of transient receptor potential channels in the mouse endometrium.

作者信息

De Clercq Katrien, Van den Eynde Charlotte, Hennes Aurélie, Van Bree Rieta, Voets Thomas, Vriens Joris

机构信息

Laboratory of Obstetrics and Experimental Gynaecology, KU Leuven, Herestraat 49 box 611, B-3000 Leuven, Belgium.

Laboratory of Ion Channel Research and TRP Research Platform Leuven (TRPLe), KU Leuven, Herestraat 49 box 802, B-3000 Leuven, Belgium.

出版信息

Hum Reprod. 2017 Mar 1;32(3):615-630. doi: 10.1093/humrep/dew344.

Abstract

STUDY QUESTION

Does mouse endometrial epithelial cells and stromal cells have a similar transient receptor potential (TRP)-channel expression profile and to that found in the human endometrium?

SUMMARY ANSWER

Mouse endometrial epithelial and stromal cells have a distinct TRP channel expression profile analogous to what has been found in human endometrium, and hence suggests the mouse a good model to investigate the role of TRP channels in reproduction.

WHAT IS KNOWN ALREADY

An optimal intercellular communication between epithelial and stromal endometrial cells is crucial for successful reproduction. Members of the TRP family were recently described in the human endometrial stroma; however their functional expression in murine endometrium remains unspecified. Furthermore, epithelial and stromal cells have distinct functions in the reproductive process, implying the possibility for a different expression profile. However, knowledge about the functional expression pattern of TRP channels in either epithelial or stromal cells is not available.

STUDY DESIGN, SIZE, DURATION: In this study, the expression pattern of TRP channels in the murine (C57BL/6 J strain) endometrium was investigated and compared to the human expression pattern. Therefore, expression was examined in uterine tissue isolated during the natural estrous cycle (n = 16) or during an induced menstrual cycle using the menstruating mouse model (n = 28). Next, the functional expression of TRP channels was assessed separately in endometrial epithelial and stromal cell populations.

PARTICIPANTS/MATERIALS, SETTING, METHODS: Quantitative RT-PCR was used to evaluate the relative mRNA expression of TRP channels in murine uterine tissue and cells. To further assess the functional expression in epithelial or stromal cells, primary endometrial cell cultures and Fura2-based calcium-microfluorimetry experiments were performed.

MAIN RESULTS AND THE ROLE OF CHANCE

The expression pattern of TRP channels during the natural estrous cycle or the induced menstrual cycle is analog to what has been shown in human samples. Furthermore, a very distinct expression pattern was observed in epithelial cells compared to stromal cells. Expression of TRPV4, TRPV6 and TRPM6 was significantly higher in epithelial cells whereas TRPV2, TRPC1/4 and TRPC6 were almost exclusively expressed in stromal cells.

LARGE SCALE DATA

N/A.

LIMITATIONS, REASONS FOR CAUTION: Although relevant mRNA levels are detected for TRPV6 and TRPM6, and TRPM4, lack of selective, available pharmacology restricted functional analysis of these ion channels.

WIDER IMPLICATIONS OF THE FINDINGS

Successful reproduction, and more specifically embryo implantation, is a dynamic developmental process that integrates many signaling molecules into a precisely orchestrated program. Here, we describe the expression pattern of TRP channels in mouse endometrium that is similar to human tissue and their restricted functionality in either stromal cells or epithelial cells, suggesting a role in the epithelial-stromal crosstalk. These results will be very helpful to identify key players involved in the signaling cascades required for successful embryo implantation. In addition, these results illustrate that mouse endometrium is a valid representative for human endometrium to investigate TRP channels in the field of reproduction.

STUDY FUNDING/COMPETING INTEREST(S): The Research Foundation-Flanders (G.0856.13 N to J.V.); the Research Council of the Katholieke Universiteit Leuven (OT/13/113 to J.V. and PF-TRPLe to T.V.); the Planckaert-De Waele fund (to J.V.);  Fonds Wetenschappelijk Onderzoek Belgium (to K.D.C. and A.H.). None of the authors have a conflict of interest.

摘要

研究问题

小鼠子宫内膜上皮细胞和基质细胞的瞬时受体电位(TRP)通道表达谱是否与人类子宫内膜相似?

总结答案

小鼠子宫内膜上皮细胞和基质细胞具有独特的TRP通道表达谱,与人类子宫内膜中的情况类似,因此表明小鼠是研究TRP通道在生殖中作用的良好模型。

已知信息

子宫内膜上皮细胞和基质细胞之间最佳的细胞间通讯对于成功生殖至关重要。TRP家族成员最近在人类子宫内膜基质中被描述;然而它们在小鼠子宫内膜中的功能表达仍未明确。此外,上皮细胞和基质细胞在生殖过程中具有不同功能,这意味着可能存在不同的表达谱。然而,关于TRP通道在上皮细胞或基质细胞中的功能表达模式尚无相关信息。

研究设计、规模、持续时间:在本研究中,研究了小鼠(C57BL/6 J品系)子宫内膜中TRP通道的表达模式,并与人类表达模式进行比较。因此,在自然发情周期(n = 16)或使用月经小鼠模型诱导的月经周期(n = 28)期间分离的子宫组织中检测表达。接下来,分别评估子宫内膜上皮细胞和基质细胞群体中TRP通道的功能表达。

参与者/材料、环境、方法:使用定量RT-PCR评估小鼠子宫组织和细胞中TRP通道的相对mRNA表达。为了进一步评估上皮细胞或基质细胞中的功能表达,进行了原代子宫内膜细胞培养和基于Fura2的钙微荧光测定实验。

主要结果及偶然性的作用

自然发情周期或诱导月经周期期间TRP通道的表达模式与人类样本中所示相似。此外,与基质细胞相比,上皮细胞中观察到非常明显的表达模式。TRPV4、TRPV6和TRPM6在上皮细胞中的表达明显更高,而TRPV2、TRPC1/4和TRPC6几乎仅在基质细胞中表达。

大规模数据

无。

局限性、谨慎原因:尽管检测到了TRPV6、TRPM6和TRPM4的相关mRNA水平,但缺乏选择性的可用药理学方法限制了对这些离子通道的功能分析。

研究结果的更广泛意义

成功生殖,尤其是胚胎着床,是一个动态发育过程,将许多信号分子整合到一个精确编排的程序中。在此,我们描述了小鼠子宫内膜中TRP通道的表达模式,其与人类组织相似,并且它们在基质细胞或上皮细胞中的功能受限,提示其在上皮-基质相互作用中的作用。这些结果将非常有助于确定成功胚胎着床所需信号级联反应中的关键参与者。此外,这些结果表明小鼠子宫内膜是在生殖领域研究TRP通道的人类子宫内膜的有效代表。

研究资金/利益冲突:弗拉芒研究基金会(给J.V.的G.0856.13 N);鲁汶天主教大学研究委员会(给J.V.的OT/13/113和给T.V.的PF-TRPLe);Planckaert-De Waele基金(给J.V.);比利时科学研究基金(给K.D.C.和A.H.)。作者均无利益冲突。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验