雌激素受体α抑制剂MPP在小鼠囊胚形成和滋养层干细胞中影响YAP核定位
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摘要
目的研究雌激素受体α(estrogen receptorα,ERα)抑制剂甲基-哌啶-吡唑(methyl-piperidino-pyrazole,MPP)在小鼠桑葚胚和滋养层干细胞(trophoblast stem cells,TSCs)中对YAP的影响。方法收集昆明(kunming,KM)小鼠8-细胞胚,置于0μmol/L(对照组)和5μmol/L(实验组)MPP中培养,分别于8h、12h和24h后收集各组桑葚胚,采用免疫荧光技术观察YAP表达,采用Real Time-PCR检测MPP处理24h后Yap mRNA表达变化;将小鼠TSCs置于0μmol/L、2.5μmol/L、5μmol/L和10μmol/L MPP中培养,48h后观察细胞形态改变,分别检测Sox2、YAP、Cdx2 mRNA和蛋白表达水平。结果小鼠8-细胞胚经MPP处理24h后,桑葚胚YAP蛋白核定位水平降低,Yap mRNA水平无显著改变;经MPP处理48h后,5μmol/L组小鼠TSCs细胞出现细胞团块,10μmol/L组细胞增殖明显受抑制;与对照组相比,5μmol/L组细胞Sox2 mRNA表达水平升高,Yap和Cdx2 mRNA水平无显著改变,团块状细胞中的YAP蛋白失去明显的核内定位,SOX2和CDX2阳性细胞的表达更加密集。结论 ERα在小鼠桑葚胚和TSCs中调控YAP核定位,其在TSCs细胞中的作用与CDX2和SOX2的表达有关。
Objective To study the effects of Estrogen Receptor alpha(ERα) inhibitor methyl-piperidino-pyrazole(MPP) on YAP localization in mouse morula and Trophoblast Stem cells(TSCs). Methods 8-cell embryos of KM mice were collected and cultured in 0 μmol/L(control group) and 5 μmol/L(experimental group) MPP, respectively. The morulae of each group were collected after 8 h, 12 h and 24 h culture, respectively. The expression of YAP was observed by immunofluorescence, and the expression of Yap m RNA was detected by Real Time-PCR after MPP treatment for 24 hours. The TSCs were cultured in 0 μmol/L, 2.5 μmol/L, 5 μmol/L and 10 μmol/L MPP. After 48 h, TSCs morphology was observed and their Sox2, Yap, Cdx2 mRNA and protein expression levels were detected. Results After treatment with MPP for 24 h, the nuclear localization level of YAP protein in morula stage embryos decreased,while the level of Yap mRNA did not change significantly. After 48 h treatment with MPP, cell clumps appeared in TSCs cells of 5μmol/L group, while the proliferation of cells in the 10 μmol/L group was significantly inhibited. Compared with the control group,the expression of Sox2 mRNA was increased in the 5 μmol/L group, however, the levels of Yap and Cdx2 mRNA didn't significantly change. The YAP protein in the cell clumps lost obvious nuclear localization and SOX2 and CDX2 positive cells were more densely expressed. Conclusion ERα regulates YAP nuclear localization in mouse morula and TSCs, and its role in TSCs is related to the expression of CDX2 and SOX2.
Objective To study the effects of Estrogen Receptor alpha(ERα) inhibitor methyl-piperidino-pyrazole(MPP) on YAP localization in mouse morula and Trophoblast Stem cells(TSCs). Methods 8-cell embryos of KM mice were collected and cultured in 0 μmol/L(control group) and 5 μmol/L(experimental group) MPP, respectively. The morulae of each group were collected after 8 h, 12 h and 24 h culture, respectively. The expression of YAP was observed by immunofluorescence, and the expression of Yap m RNA was detected by Real Time-PCR after MPP treatment for 24 hours. The TSCs were cultured in 0 μmol/L, 2.5 μmol/L, 5 μmol/L and 10 μmol/L MPP. After 48 h, TSCs morphology was observed and their Sox2, Yap, Cdx2 mRNA and protein expression levels were detected. Results After treatment with MPP for 24 h, the nuclear localization level of YAP protein in morula stage embryos decreased,while the level of Yap mRNA did not change significantly. After 48 h treatment with MPP, cell clumps appeared in TSCs cells of 5μmol/L group, while the proliferation of cells in the 10 μmol/L group was significantly inhibited. Compared with the control group,the expression of Sox2 mRNA was increased in the 5 μmol/L group, however, the levels of Yap and Cdx2 mRNA didn't significantly change. The YAP protein in the cell clumps lost obvious nuclear localization and SOX2 and CDX2 positive cells were more densely expressed. Conclusion ERα regulates YAP nuclear localization in mouse morula and TSCs, and its role in TSCs is related to the expression of CDX2 and SOX2.
引文
[1]Cheng X, Xu S, Song C, et al. Roles of eralpha during mouse trophectoderm lineage differentiation:Revealed by antagonist and agonist of eralpha. Dev Growth Differ, 2016, 58(3):327-338.
[2]Sasaki H. Position-and polarity-dependent hippo signaling regulates cell fates in preimplantation mouse embryos. Semin Cell Dev Biol, 2015, 47-48(2015):80-87.
[3]Britschgi A, Duss S, Kim S, et al. The hippo kinases lats1and 2 control human breast cell fate via crosstalk with eralpha. Nature, 2017, 541(7638):541-545.
[4]Frum T, Ralston A. Cell signaling and transcription factors regulating cell fate during formation of the mouse blastocyst. Trends Genet, 2015, 31(7):402-410.
[5]Yu C, Ji SY, Dang YJ, et al. Oocyte-expressed yes-associated protein is a key activator of the early zygotic genome in mouse. Cell Res, 2016, 26(3):275-287.
[6]Liu X, Wang C, Liu W, et al. Distinct features of h3k4me3and h3k27me3 chromatin domains in pre-implantation embryos. Nature, 2016, 537(7621):558-562.
[7]Kidder BL, Palmer S. Examination of transcriptional networks reveals an important role for tcfap2c, smarca4, and eomes in trophoblast stem cell maintenance. Genome Res,2010, 20(4):458-472.
[8]Festuccia N, Owens N, Navarro P. Esrrb, an estrogen-related receptor involved in early development, pluripotency, and reprogramming. FEBS Lett, 2018, 592(6):852-877.
[9]Hemberger M, Udayashankar R, Tesar P, et al. Elf5-enforced transcriptional networks define an epigenetically regulated trophoblast stem cell compartment in the human placenta.Hum Mol Genet, 2010, 19(12):2456-2467.
[10] Prudhomme J, Morey C. Epigenesis and plasticity of mouse trophoblast stem cells. Cell Mol Life Sci, 2016, 73(4):757-774.
[11] Kim NG, Koh E, Chen X, et al. E-cadherin mediates contact inhibition of proliferation through hippo signaling-pathway components. P Natl Acad Sci USA, 2011, 108(29):11930-11935.
[12] Adachi K, Nikaido I, Ohta H, et al. Context-dependent wiring of sox2 regulatory networks for self-renewal of embryonic and trophoblast stem cells. Mol Cell, 2013, 52(3):380-392.
[2]Sasaki H. Position-and polarity-dependent hippo signaling regulates cell fates in preimplantation mouse embryos. Semin Cell Dev Biol, 2015, 47-48(2015):80-87.
[3]Britschgi A, Duss S, Kim S, et al. The hippo kinases lats1and 2 control human breast cell fate via crosstalk with eralpha. Nature, 2017, 541(7638):541-545.
[4]Frum T, Ralston A. Cell signaling and transcription factors regulating cell fate during formation of the mouse blastocyst. Trends Genet, 2015, 31(7):402-410.
[5]Yu C, Ji SY, Dang YJ, et al. Oocyte-expressed yes-associated protein is a key activator of the early zygotic genome in mouse. Cell Res, 2016, 26(3):275-287.
[6]Liu X, Wang C, Liu W, et al. Distinct features of h3k4me3and h3k27me3 chromatin domains in pre-implantation embryos. Nature, 2016, 537(7621):558-562.
[7]Kidder BL, Palmer S. Examination of transcriptional networks reveals an important role for tcfap2c, smarca4, and eomes in trophoblast stem cell maintenance. Genome Res,2010, 20(4):458-472.
[8]Festuccia N, Owens N, Navarro P. Esrrb, an estrogen-related receptor involved in early development, pluripotency, and reprogramming. FEBS Lett, 2018, 592(6):852-877.
[9]Hemberger M, Udayashankar R, Tesar P, et al. Elf5-enforced transcriptional networks define an epigenetically regulated trophoblast stem cell compartment in the human placenta.Hum Mol Genet, 2010, 19(12):2456-2467.
[10] Prudhomme J, Morey C. Epigenesis and plasticity of mouse trophoblast stem cells. Cell Mol Life Sci, 2016, 73(4):757-774.
[11] Kim NG, Koh E, Chen X, et al. E-cadherin mediates contact inhibition of proliferation through hippo signaling-pathway components. P Natl Acad Sci USA, 2011, 108(29):11930-11935.
[12] Adachi K, Nikaido I, Ohta H, et al. Context-dependent wiring of sox2 regulatory networks for self-renewal of embryonic and trophoblast stem cells. Mol Cell, 2013, 52(3):380-392.