Leno-Durán E, Ruiz-Magaña M J, Muñoz-Fernández R, Requena F, Olivares E G, Ruiz-Ruiz C
Unidad de Inmunología, IBIMER, Centro de Investigación Biomédica, Universidad de Granada, Avda. del Conocimiento s/n, Granada 18016, Spain.
Instituto de Parasitología y Biomedicina 'López-Neyra', CSIC, Granada 18016, Spain.
Hum Reprod. 2014 Oct 10;29(10):2269-77. doi: 10.1093/humrep/deu202. Epub 2014 Aug 14.
Is there a relationship between decidualization and apoptosis of decidual stromal cells (DSC)?
Decidualization triggers the secretion of soluble factors that induce apoptosis in DSC.
The differentiation and apoptosis of DSC during decidualization of the receptive decidua are crucial processes for the controlled invasion of trophoblasts in normal pregnancy. Most DSC regress in a time-dependent manner, and their removal is important to provide space for the embryo to grow. However, the mechanism that controls DSC death is poorly understood.
STUDY DESIGN, SIZE, DURATION: The apoptotic response of DSC was analyzed after exposure to different exogenous agents and during decidualization. The apoptotic potential of decidualized DSC supernatants and prolactin (PRL) was also evaluated.
PARTICIPANTS/MATERIALS, SETTING, METHODS: DSC lines were established from samples of decidua from first trimester pregnancies. Apoptosis was assayed by flow cytometry. PRL production, as a marker of decidualization, was determined by enzyme-linked immunosorbent assay.
DSCs were resistant to a variety of apoptosis-inducing substances. Nevertheless, DSC underwent apoptosis during decidualization in culture, with cAMP being essential for both apoptosis and differentiation. In addition, culture supernatants from decidualized DSC induced apoptosis in undifferentiated DSC, although paradoxically these supernatants decreased the spontaneous apoptosis of decidual lymphocytes. Exogenously added PRL did not induce apoptosis in DSC and an antibody that neutralized the PRL receptor did not decrease the apoptosis induced by supernatants.
LIMITATIONS, REASONS FOR CAUTIONS: Further studies are needed to examine the involvement of other soluble factors secreted by decidualized DSC in the induction of apoptosis.
The present results indicate that apoptosis of DSC occurs in parallel to differentiation, in response to decidualization signals, with soluble factors secreted by decidualized DSC being responsible for triggering cell death. These studies are relevant in the understanding of how the regression of decidua, a crucial process for successful pregnancy, takes place.
STUDY FUNDING/COMPETING INTERESTS: This work was supported by the Consejería de Economía, Innovación y Ciencia, Junta de Andalucía (Grant CTS-6183, Proyectos de Investigación de Excelencia 2010 to C.R.-R.) and the Instituto de Salud Carlos III, Ministerio de Economía y Competitividad, Spain (Grants PS09/00339 and PI12/01085 to E.G.O.). E.L.-D. was supported by fellowships from the Ministerio de Educación y Ciencia, Spain and the University of Granada. The authors have no conflict of interest.
蜕膜化与蜕膜基质细胞(DSC)凋亡之间是否存在关联?
蜕膜化触发可溶性因子的分泌,这些因子可诱导DSC凋亡。
在接受性蜕膜蜕膜化过程中,DSC的分化和凋亡是正常妊娠中滋养层细胞受控侵袭的关键过程。大多数DSC以时间依赖性方式退化,它们的清除对于为胚胎生长提供空间很重要。然而,控制DSC死亡的机制尚不清楚。
研究设计、规模、持续时间:分析了DSC在暴露于不同外源性物质后以及蜕膜化过程中的凋亡反应。还评估了蜕膜化DSC上清液和催乳素(PRL)的凋亡潜力。
参与者/材料、设置、方法:从妊娠早期蜕膜样本中建立DSC系。通过流式细胞术检测凋亡。通过酶联免疫吸附测定法测定PRL的产生,作为蜕膜化的标志物。
DSC对多种凋亡诱导物质具有抗性。然而,DSC在培养的蜕膜化过程中发生凋亡,cAMP对于凋亡和分化均至关重要。此外,蜕膜化DSC的培养上清液可诱导未分化DSC凋亡,尽管矛盾的是这些上清液可降低蜕膜淋巴细胞的自发凋亡。外源性添加的PRL未诱导DSC凋亡,中和PRL受体的抗体也未降低上清液诱导的凋亡。
局限性、谨慎的原因:需要进一步研究以检查蜕膜化DSC分泌的其他可溶性因子在凋亡诱导中的作用。
目前的结果表明,DSC的凋亡与分化同时发生,以响应蜕膜化信号,蜕膜化DSC分泌的可溶性因子负责触发细胞死亡。这些研究对于理解蜕膜退化这一成功妊娠的关键过程如何发生具有重要意义。
研究资金/竞争利益:这项工作得到了安达卢西亚自治区经济、创新和科学委员会(资助号CTS - 6183,2010年卓越研究项目授予C.R.-R.)以及西班牙经济和竞争力部卡洛斯三世健康研究所(资助号PS09/00339和PI12/01085授予E.G.O.)的支持。E.L.-D.得到了西班牙教育和科学部以及格拉纳达大学的奖学金支持。作者没有利益冲突。