Immunolocalization of PCNA, Ki67, p27 and p57 in normal and dexamethasone-induced intrauterine growth restriction placental development in rat

Unek G., Ozmen A., Kipmen-Korgun D., KORGUN E. T.

ACTA HISTOCHEMICA, cilt.114, sa.1, ss.31-40, 2012 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 114 Sayı: 1
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1016/j.acthis.2011.02.002
  • Dergi Adı: ACTA HISTOCHEMICA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.31-40
  • Anahtar Kelimeler: Placental development, Intrauterine growth retardation, PCNA, Ki67, p27, p57, Rat, CDK INHIBITORS P27(KIP1), CELL-CYCLE REGULATORS, PROTEIN-KINASES, LATE PREGNANCY, KI-67 PROTEIN, FETAL-GROWTH, EXPRESSION, P57(KIP2), GLUCOCORTICOIDS, HYPERTENSION
  • Akdeniz Üniversitesi Adresli: Evet

Özet

Intrauterine growth restriction (IUGR) is a major clinical problem which causes perinatal morbidity and mortality. Although fetuses with IUGR form a heterogeneous group, a major etiological factor is abnormal placentation. Despite the fact that placental development requires the coordinated action of trophoblast proliferation and differentiation, there are few studies on cell cycle regulators, which play the main roles in the coordination of these events. Moreover it is still not determined how mechanisms of coordination of proliferation and differentiation are influenced by dexamethasone-induced IUGR in the placenta. The aim of the study was to investigate the spatial and temporal immunolocalization of proliferating cell nuclear antigen (PCNA), Ki67, p27 and p57 in normal and IUGR placental development in pregnant Wistar rats. The study demonstrated altered expressions of distinct cell cycle proteins and cyclin dependent kinase inhibitors (CKIs) in IUGR placental development compared to control placental development. We found reduced immunostaining of PCNA and Ki67 and increased immunostaining of p27 and p57 in the dexamethasone-induced IUGR placental development compared to control placental development. In conclusion, our data show that the cell populations in the placenta stain for a number of cell cycle related proteins and that these staining patterns change as a function of both gestational age and abnormal placentation. (C) 2011 Elsevier GmbH. All rights reserved.