| Literature DB >> 23761267 |
Niroshani A Pathirage1, Melanie Cocquebert, Yoel Sadovsky, Mohamed Abumaree, Ursula Manuelpillai, Anthony Borg, Rosemary J Keogh, Shaun P Brennecke, Daniele Evain-Brion, Thierry Fournier, Bill Kalionis, Padma Murthi.
Abstract
Abnormal trophoblast function is associated with human fetal growth restriction (FGR). Targeted disruption of homeobox gene transforming growth β-induced factor (TGIF-1) results in placental dysfunction in the mouse. The role of human TGIF-1 in placental cell function is unknown. The aims of this study were to determine the expression of TGIF-1 in human idiopathic FGR-affected placentae compared with gestation-matched controls (GMC), to elucidate the functional role of TGIF-1 in trophoblasts and to identify its downstream targets. Real-time PCR and immunoblotting revealed that TGIF-1 mRNA and protein expression was significantly increased in FGR-affected placentae compared with GMC (n = 25 in each group P < 0.05). Immunoreactive TGIF-1 was localized to the villous cytotrophoblasts, syncytiotrophoblast, microvascular endothelial cells and in scattered stromal cells in both FGR and GMC. TGIF-1 inactivation in BeWo cells using two independent siRNA resulted in significantly decreased mRNA and protein of trophoblast differentiation markers, human chorionic gonadotrophin (CGB/hCG), syncytin and 3β-hydroxysteroid dehydrogenase/3β-honest significant difference expression. Our data demonstrate that homeobox gene TGIF-1 is a potential up-stream regulator of trophoblast differentiation and the altered TGIF-1 expression may contribute to aberrant villous trophoblast differentiation in FGR.Entities:
Keywords: fetal growth restriction; gene expression; homeobox genes; placenta; pregnancy
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Year: 2013 PMID: 23761267 DOI: 10.1093/molehr/gat042
Source DB: PubMed Journal: Mol Hum Reprod ISSN: 1360-9947 Impact factor: 4.025