Is there a relationship between PCNA expression and diabetic placental development during pregnancy?


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Acar N., Korgun E. T., Çaylı S., Şahin Z., Demir R., Üstünel İ.

ACTA HISTOCHEMICA, cilt.110, sa.5, ss.408-417, 2008 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 110 Sayı: 5
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1016/j.acthis.2007.11.011
  • Dergi Adı: ACTA HISTOCHEMICA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.408-417
  • Anahtar Kelimeler: diabetes, placenta, rat, PCNA, immunohistochemistry, Western blot, CELL NUCLEAR ANTIGEN, GROWTH-RETARDATION, DISTRIBUTION PATTERNS, PROTEIN-TURNOVER, RAT PLACENTA, FETAL-GROWTH, IN-VITRO, DNA, DIFFERENTIATION, REGULATORS
  • Akdeniz Üniversitesi Adresli: Evet

Özet

We aimed to investigate the distribution pattern of proliferating cell nuclear antigen (PCNA) by immunohistochemistry and Western blot in placentas of control and diabetic rats at different stages of pregnancy. It is still not clear how proliferation is coordinated and how this coordination is affected by diabetes in the placenta. Diabetes was induced by streptozocin on the first day of pregnancy. Animals were sacrificed on days 11, 13, 17 and 21 of pregnancy. In control placentas immunolabeling intensity of PCNA was the highest on days 11 and 13 of pregnancy and decreased with progression of pregnancy. In the diabetic groups immunolabeling was less intense on days 11 and 13 of pregnancy compared to controls. However, in parallel. with placental weights, PCNA immunopositivity was more intense in diabetic groups than control groups on days 17 and 21 of pregnancy, and the difference was statistically significant on day 17. According to Western Not data, on days 11 and 13 of pregnancy the amount of PCNA was greater in control groups than in the diabetics, whereas it was greater in diabetic groups than the controls on days 17 and 21 of pregnancy. We conclude that PCNA may play a rote in abnormal placenta formation resulting from diabetes.