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[M. Immunology-5]



               The function of INHBB with regard to pregnancy disorder,


                preeclampsia in human trophoblast cell line, Swan71 cell




          Hee-Na Jeong¹˙#, Eun-Bee Jeong¹˙#, Se-Jin Ahn¹, Ga-Eun Yoo¹, Hae-Ryeong Lim¹˙*, Deug-Chan Lee¹˙*

         ¹Department of Medical biotechnology, College of Biomedical Science, Kangwon National University, Chuncheon-

                                         si, Gangwon-do 200-701, Republic of Korea




        Preeclampsia is a serious pregnancy disorder characterized by gestational hypertension and proteinuria. During the
        early  stage  of  pregnancy,  trophoblast  surrounding  the  embryo  attach  to  and  invade the uterus. Trophoblasts

        subsequently perform spiral artery remodeling by interacting with a variety off actors such as hormones, cytokines,

        and  growth  factors.  MicroRNAs  are  small(21-to  23-nucleotide),  single-stranded  RNA  molecules.  They  bind  to
        messenger RNA which has complementary sequences and regulate gene expression at the post-transcription level.
        In preeclampsia patents over express the miR-210 more than normal pregnancy, we identified that regulated genes

        by miR-210 in human first-trimester trophoblast cell line. In present study, we focused on inhibin beta B (INHBB)
        which is one of the down-regulated genes by miR-210. We found that INHBB is a direct miR-210 target, down

        regulating INHBB  mRNA and INHBB  protein  expression.  This miR-210  induced  decrease  in  INHBB  expression
        suppressed trophoblast cell invasion. Therefore down-regulation of INHBB, a direct miR-210 target, may contribute

        to preeclampsia pathogenesis by attenuating trophoblast invasiveness.
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