Street M E, Seghini P, Ziveri M A, Fieni S, Volta C, Neri T M, Viani I, Bacchi-Modena A, Bernasconi S
Department of Paediatrics, University of Parma, Via Gramsci, 14, 43100 Parma, Italy.
Growth Horm IGF Res. 2006 Oct-Dec;16(5-6):365-72. doi: 10.1016/j.ghir.2006.09.007. Epub 2006 Nov 13.
The integrity of the insulin-like growth factor (IGF) system is essential for normal fetal growth. Cytokine and IGF-IGFBP relationships have been shown in specific tissues, but it is unknown whether these occur in the placenta. We aimed to assess possible differences in the IGF system depending on gestational age (GA) from week 35 to 40, and to study relationships of IL-6 with components of the IGF system in the placenta and newborn infant. We followed 32 normal births and collected whole villous tissue and cord serum. Total RNA was extracted from the placenta samples, reverse transcribed and then real-time quantitative (TaqMan) RT-PCR was performed to quantify cDNA for IGF-I, IGF-II, IGFBP-1, IGFBP-2 and IL-6. The corresponding proteins were assayed in placenta lysates and cord serum using specific commercial kits. Two groups of subjects (Group 1, 35-37 weeks GA, N=12 and Group 2, 38-40 weeks GA, N=20) were studied. In placenta, IGF-I mRNA was more abundant than IGF-II mRNA at all times and together with IGFBP-1mRNA were less expressed at term. IGFBP-2 and IL-6 mRNAs were higher after week 37 GA. IL-6 and IGFBP-2 gene expression were closely related. The corresponding proteins showed similar differences to the genes but IGF-I was undetectable in the lysates, whereas IGF-II was abundant. IGFBP-2 concentrations were very high and greater than those of IGFBP-1. In the newborn, no difference was seen in any cord serum protein after week 35 GA. IGFBP-1 was negatively correlated with parameters of neonatal size. In conclusion, this study reports new insights into IL-6, IGF-IGFBP relationships within the human placenta and shows the importance of comparing subjects with the same GA.
胰岛素样生长因子(IGF)系统的完整性对胎儿正常生长至关重要。细胞因子与IGF-IGFBP的关系已在特定组织中得到证实,但在胎盘中是否存在这些关系尚不清楚。我们旨在评估35至40周胎龄(GA)时IGF系统可能存在的差异,并研究白细胞介素-6(IL-6)与胎盘和新生儿中IGF系统各成分之间的关系。我们追踪了32例正常分娩病例,并收集了全绒毛组织和脐带血清。从胎盘样本中提取总RNA,进行逆转录,然后进行实时定量(TaqMan)RT-PCR以定量IGF-I、IGF-II、IGFBP-1、IGFBP-2和IL-6的cDNA。使用特定的商业试剂盒在胎盘裂解物和脐带血清中检测相应的蛋白质。研究了两组受试者(第1组,GA为35 - 37周,N = 12;第2组,GA为38 - 40周,N = 20)。在胎盘中,IGF-I mRNA在所有时间都比IGF-II mRNA更丰富,并且与IGFBP-1 mRNA在足月时表达较少。GA在37周后,IGFBP-2和IL-6 mRNA水平升高。IL-6与IGFBP-2基因表达密切相关。相应的蛋白质表现出与基因相似的差异,但在裂解物中未检测到IGF-I,而IGF-II含量丰富。IGFBP-2浓度非常高且高于IGFBP-1。在新生儿中,GA在35周后,脐带血清中的任何蛋白质均无差异。IGFBP-1与新生儿大小参数呈负相关。总之,本研究报告了关于人胎盘内IL-6、IGF-IGFBP关系的新见解,并显示了比较相同GA受试者的重要性。