Unek Gozde, Ozmen Asli, Ozekinci Murat, Sakinci Mehmet, Korgun Emin Turkay
Department of Histology and Embryology, Medical Faculty, Akdeniz University, 07070 Antalya, Turkey.
Department of Obstetrics and Gynecology, Medical Faculty, Akdeniz University, 07070 Antalya, Turkey.
Acta Histochem. 2014 Apr;116(3):493-502. doi: 10.1016/j.acthis.2013.10.007. Epub 2013 Nov 16.
Placental development involves a series of events that depend on the coordinated action of proliferation, differentiation and invasion of trophoblasts. Studies on cell cycle related proteins controlling these events are fairly limited. It is still not fully determined how placental tissue proliferation is affected by intrauterine growth retardation (IUGR). Information on cell cycle related proteins that control these events is limited and how they are affected in IUGR is not fully understood. The aim of this study was to understand the role of cell cycle regulators in IUGR placentas and to determine the spatio-temporal immunolocalization of these cell cycle regulators in human IUGR and normal term placentas. Placental samples were stained immunohistochemically with PCNA, Ki67, cyclin D3, p27 and p57 antibodies and were examined by light microscopy. In all regions of IUGR placentas, PCNA, Ki67 and cyclin D3 staining intensities were statistically significantly decreased compared to normal controls. p27 staining intensity of the IUGR group was statistically significantly increased in villous parts and chorionic plates in comparison with the normal term placentas. Moreover, p57 staining intensity was statistically significantly increased in all parts of the IUGR group compared to controls. The observed placental abnormalities in IUGR placentas may be associated with arrest mechanisms affecting cell proliferation and cell cycle alterations in IUGR.
胎盘发育涉及一系列依赖于滋养层细胞增殖、分化和侵袭协同作用的事件。关于控制这些事件的细胞周期相关蛋白的研究相当有限。目前仍未完全确定宫内生长受限(IUGR)如何影响胎盘组织增殖。关于控制这些事件的细胞周期相关蛋白的信息有限,且它们在IUGR中如何受到影响尚不完全清楚。本研究的目的是了解细胞周期调节因子在IUGR胎盘中的作用,并确定这些细胞周期调节因子在人类IUGR胎盘和足月正常胎盘中的时空免疫定位。胎盘样本用PCNA、Ki67、细胞周期蛋白D3、p27和p57抗体进行免疫组织化学染色,并通过光学显微镜检查。与正常对照组相比,IUGR胎盘所有区域的PCNA、Ki67和细胞周期蛋白D3染色强度在统计学上显著降低。与足月正常胎盘相比,IUGR组绒毛部分和绒毛膜板的p27染色强度在统计学上显著增加。此外,与对照组相比,IUGR组所有部位的p57染色强度在统计学上显著增加。IUGR胎盘中观察到的胎盘异常可能与影响IUGR细胞增殖和细胞周期改变的停滞机制有关。