Expressional and epigenetic alterations of placental serine protease inhibitors -: SERPINA3 is a potential marker of preeclampsia

被引:107
作者
Chelbi, Sonia T.
Mondon, Francoise
Jammes, Helene
Buffat, Christophe
Mignot, Therese-Marie
Tost, Jorg
Busato, Florence
Gut, Ivo
Rebourcet, Regis
Laissue, Paul
Tsatsaris, Vassili
Goffinet, Francois
Rigourd, Virginie
Carbonne, Bruno
Ferre, Francoise
Vaiman, Daniel
机构
[1] Univ Paris 05, Fac Med, Equipe 21,IFR Alfred Jost, Unite INSERM 567 UMR CNRS 8104, F-75014 Paris, France
[2] INRA, PHASE Dept, Jouy En Josas, France
[3] Univ Mediterranee, Fac Med, Marseille, France
[4] Hop Conception, AP HM, Serv Neonatol, Marseille, France
[5] Ctr Natl Genotypage, Lab Epigenet, Evry, France
[6] Univ Paris 05, Serv Gynecol Obstet, Fac Med, APHP,Hop Cochin, F-75014 Paris, France
[7] Hop St Antoine, Serv Gynecol Obstet, F-75571 Paris, France
[8] INRA, Anim Genet Dept, Jouy En Josas, France
关键词
preeclampsia; intrauterine growth restriction; placenta; serine protease inhibitors; epigenetics;
D O I
10.1161/01.HYP.0000250831.52876.cb
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Preeclampsia is the major pregnancy-induced hypertensive disorder. It modifies the expression profile of placental genes, including several serine protease inhibitors (SERPINs). The objective of this study was to perform a systematic expression analysis of these genes in normal and pathological placentas and to pinpoint epigenetic alterations inside their promoter regions. Expression of 18 placental SERPINs was analyzed by quantitative RT-PCR on placentas from pregnancies complicated by preeclampsia, intrauterine growth restriction, or both and was compared with normal controls. SERPINA3, A5, A8, B2, B5, and B7 presented significant differences in expression in >= 1 pathological situation. In parallel, the methylation status of the CpG islands located in their promoter regions was studied on a sample of control and preeclamptic placentas. Ten SERPIN promoters were either totally methylated or totally unmethylated, whereas SERPINA3, A5, and A8 presented complex methylation profiles. For SERPINA3, the analysis was extended to 81 samples and performed by pyrosequencing. For the SERPINA3 CpG island, the average methylation level was significantly diminished in preeclampsia and growth restriction. The hypomethylated CpGs were situated at putative binding sites for developmental and stress response (hypoxia and inflammation) factors. Our results provide one of the first observations of a specific epigenetic alteration in human placental diseases and provide new potential markers for an early diagnosis.
引用
收藏
页码:76 / 83
页数:8
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