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组蛋白去乙酰化酶1蛋白在早期自然流产绒毛和蜕膜组织中的表达 被引量:1

Expression of HDAC1 protein in chorionic villi and decidua of early spontaneous abortion
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摘要 目的:探讨组蛋白去乙酰化酶1(HDAC1)蛋白在早期自然流产发生中的病理生理作用及临床意义。方法:应用免疫组织化学和Western blot法检测早期自然流产和早期正常妊娠者绒毛及蜕膜组织中HDAC1蛋白的表达。结果:免疫组化示:HDAC1主要定位于绒毛细胞滋养细胞、合体滋养细胞和子宫蜕膜细胞、腺上皮细胞的胞核;早期自然流产绒毛组织中HDAC1的表达强度低于早期正常妊娠组,而蜕膜组织中,早期自然流产组织HDAC1的表达强度高于正常妊娠组,差异均有统计学意义(P均<0.05)。Westernblot示:早期自然流产绒毛组织中HDAC1蛋白的相对表达量为1.38±0.63,明显低于正常妊娠组(1.92±0.82),差异有统计学意义(P<0.05);而早期自然流产蜕膜组织中HDAC1蛋白的相对表达量为1.02±0.53,明显高于正常妊娠组(0.71±0.36),差异有统计学意义(P<0.05)。结论:HDAC1在早期自然流产绒毛和蜕膜组织中的异常表达可能在早期自然流产的发生、发展中起重要作用。 Objective:To study the pathophysiological roles and clinical significance of HDAC1 protein in chorionic villi and decidua of patients with early spontaneous abortion.Methods:The expression of HDAC1 in chorionic villi and decidua of early spontaneous abortion and normal pregnancy was detected using immunohistochemistry and Western-blot.Results:Immunoreactive staining of HDAC1 was predominantly located in the nuclei of syneytiotrophooblast,cytotrophoblast cell of chorionic villi,and decidual cell,glandular epithelium cell of decidua.The intensity of HDAC1 staining in the chorionic villi of early spontaneous abortion was lower than that of normal pregnancy,while the intensity of HDAC1 staining in decidua was higher than that of normal pregnancy,and the differences were significant(P0.05).Western-blot showed that HDAC1 protein level in the chorionic villi of early spontaneous abortion was significantly lower than that of normal pregnancy(1.38±0.63 vs 1.92±0.82,P0.05).HDAC1 protein level in the decidua of early spontaneous abortion was significantly higher than that of normal pregnancy(1.02±0.53 vs 0.71±0.36,P0.05).Conclusion:Abnormal expression of HDAC1 in the chorionic villi and decidua may play an important role in the process of early spontaneous abortion.
出处 《现代妇产科进展》 CSCD 北大核心 2011年第9期726-729,共4页 Progress in Obstetrics and Gynecology
关键词 早期自然流产 绒毛 蜕膜 组蛋白去乙酰化酶1 Early spontaneous abortion Chorionic villi Decidua Histone deacetylases
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参考文献15

  • 1Krusche CA,Vloet AJ,Classen-Linke I,et al. Class I his- tone deacetylase expression in the human cyclic endome- trium and endometrial adenocarcinomas [ J ]. Hum Reprod, 2007,22 : 2956-2966.
  • 2Brunmeir R, Lagger S, Seiser C. Histone deacety|ase H- DAC1/HDAC2-controlled embryonic development and cell differentiation[J]. Int J Dev Biol,2009,53:275-289.
  • 3Taunton J, Hassig CA, Schreiber SL. A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3 P [ J ]. Science, 1996,272:408-411.
  • 4Hayashi A, ttoriuchi A, Kikuchi N, et al. Type-specific roles of bistone deacetylase (HDAC) overexpression in o- varian careinoma:HDAC1 enhances cell proliferation and HDAC3 stimulates cell migration with downregulation of E-cadherin[J]. Int J Cancer ,2010,127 : 1332-1346.
  • 5任媛媛,王雅杰.HDAC1和DNMT1蛋白在乳腺癌中的表达及临床意义[J].临床肿瘤学杂志,2010,15(2):101-105. 被引量:10
  • 6Senese S, Zaragoza K, Minardi S, et al. Role for histone deacetylase 1 in human tumor cell proliferation [ J ]. Mol Cell Bio1,2007 ,27 :4784-4795.
  • 7Wu Y, Guo SW. Histone deacetylase inhibitors trichostatin A and valproic acid induce cell cycle arrest and p21 ex- pression in immortalized human endometrial stromal cells [J]. Reproductive ,2008,137 : 198-203.
  • 8Wu Y, Gno SW. Inhibition of proliferation of endometrial stromal cells by triehostatin A, RU486, CDB-2914, N- Acetyleysteine,and ICI 182780 [J]. Gyneeol Obstet Invest, 2006,62 : ! 93-205.
  • 9Lagger G, O'Carroll D, Rembold M, et al. Essential function of histone deacetylasel in proliferation control and CDK inhibitor repression [ J ]. EMBO J, 2002,21 : 2672- 2681.
  • 10Dovey OM,Foster CT,Cowley SM. Histone deacetylase 1 (HDAC1), but not HDAC2, controls embryonic stem cell differentiation[J].Proc Natl Acad Sci U S A,2010, 107 : 8242-8247.

二级参考文献30

  • 1高洁,孙月玲,余志英,孙波.自然流产绒毛及蜕膜细胞凋亡的基因调控研究[J].热带医学杂志,2007,7(5):442-444. 被引量:3
  • 2Kokawa K,Shikone T.et al.Apoptosis in human chorionic villi and deciduas during normal embryonic development and spontaneous abortion in the first trimester[J].Placenta.1998,19(1):21-26.
  • 3Kucera E,gonig F,Tang LS,et al.Bcl-2 expression as a novel immunohistoehemical marker for ruptured tubal ectopic pregnancy[J].Hum Reprod,2001,16(6):1286-1290.
  • 4Coopersmith CM,chang KC,Swamson PE,et al.OverexPression of Bcl-2 in the imestinal epithelium improves survival in septic mice[J].Crit Care Med,2002.30(1):195-201.
  • 5Jacob T,Ascher E,Hingorani A,et al.Olycine prevents the induction of apoptosis attributed to mesenterle ischemia/reperfusion injury in a ratmodel[J].Surgery,2003,134(3):457-466.
  • 6Lea RG,AI Sharekh N,Tuippala M,et al.The immunolocalisation of Bcl-2 at the maternal-fetal interface in healthy and falling pregnancies[J].Human Reprod.1997,12(1):153-158.
  • 7Chan CC.Lao TT,Cheung AN.Apoptotic and profliferative activities in first trimester placenta[J].Placenta,1999,20(2-3):223-227.
  • 8Shiraishi H,Hayakawa S,Satoh K.Murine experimental abortion by IL-2 adminstration is caused by activation of eytotoxic T lymphocytes and planeental apoptosis[J].J Clin Lab Immunol,1996,48(3):93.
  • 9Taunton J, Hassig CA, Schreiber SL. A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p [J]. Science, 1996, 272(5260) :408 -411.
  • 10Luczak MW, Jagodzinski PP. The role of DNA methylation in cancer development [ J ]. Folia Histochem Cytobiol, 2006, 44 (3) :143 -154.

共引文献14

同被引文献29

  • 1Branch DW, Gibson M, Silver RM. Clinical practice.Recurrent miscarriage [J]. N Engl J Med, 2010, 363 :1740-1747.
  • 2Paria BC,Lim H. Das SK,et al. Molecular signaling inuterine receptivity for implantation[J]. Semin Cell Dev Biol,2000,11:67-76.
  • 3Song L,Tuan RS. MicroRNAs and cell differentiation inmammalian development [J]. Birth Defects Res C EmbryoToday,2006,78:140-149.
  • 4Banno K,Kisu I, Yanokura M,et al. Epigenetics and geneticsin endometrial cancer: new carcinogenic mechanisms andrelationship with clinical practice[J]. Epigenomics, 2012, 4 :147-162.
  • 5Chavatte-Palmer P,Camous S,Jammes H, et al. Review:Placental perturbations induce the developmentalabnormalities often observed in bovine somatic cell nucleartransfer[J]. Placenta.2012,33 [Suppl] : S99-S104.
  • 6Cantone I,Fisher AG. Epigenetic programming andreprogramming during development[J], Nat Struct Mol Biol,2013,20:282-289.
  • 7Hanna CW,McFadden DE,Robinson WP. DNA methylationprofiling of placental villi from karyotypically normalmiscarriage and recurrent miscarriage 匸J]. Am J Pathol.2013,182:2276-2284.
  • 8Yin IJ,Zhang Y,LvP P,et al. Insufficient maintenance:DNAmethylation is associated with abnormal embryonicdevelopment[J/OL]. BMC Med,2012,10:26.
  • 9Jiang L,Zhang J , Wang J,et al. Sperm, but not oocyte,DNAmethylome is inherited by zebrafish early embryos[J]. Cell,2013,153:773-784.
  • 10Rotondo JC, Bosi S, Bazzan E, et al. Methylenetetrahydrofolatereductase gene promoter hypermethylation in semen samples of1 i .infertile couples correlates with recurrent spontaneous abortion[J]. Hum Reprod,2012,27:3632-3638.

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