State Key Laboratory of Reproductive Medicine, Nanjing Maternity and Child Health Care Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Yancheng No. 1 People's Hospital Affiliated to Nantong University, Nantong, China.
Proteomics Clin Appl. 2016 Nov;10(11):1122-1131. doi: 10.1002/prca.201600046. Epub 2016 Aug 1.
Offspring obesity is one of long-term complications of gestational diabetes mellitus (GDM). The aim of this study is to identify proteins differentially expressed in the umbilical vein blood plasma, which could become markers for early diagnosis of childhood obesity.
Umbilical vein plasma samples were collected from 30 control and 30 GDM patients in 2007-2008 whose offspring were suffering from obesity at 6-7 years old. Multiplexed isobaric tandem mass tag labeling combined with LC-MS/MS was used to identify differentially expressed proteins. Ingenuity pathway analysis was performed to identify canonical pathways, biological functions, and networks of interacting proteins. Western blotting was used to verify the expression of three selected proteins.
A total of 318 proteins were identified, of which 12 proteins were upregulated in GDM group while 24 downregulated. Lipid metabolism was the top category identified by ingenuity pathway analysis. Three randomly chosen proteins were validated by Western blotting, which were consistent with LC-MS.
There are significant differences of protein profile in the umbilical vein blood plasma between normal and GDM patients with obese offspring. The results indicate that a variety of proteins and biological mechanisms may contribute to childhood obesity.
子女肥胖是妊娠期糖尿病(GDM)的长期并发症之一。本研究旨在鉴定脐静脉血浆中差异表达的蛋白质,这些蛋白质可能成为儿童肥胖早期诊断的标志物。
2007 年至 2008 年间,收集了 30 名对照和 30 名 GDM 患者的脐静脉血浆样本,这些患者的子女在 6-7 岁时患有肥胖症。采用多重等压串联质量标签标记联合 LC-MS/MS 技术鉴定差异表达蛋白。采用 ingenuity 通路分析鉴定信号通路、生物学功能和相互作用蛋白网络。采用 Western blot 验证 3 种选定蛋白的表达情况。
共鉴定出 318 种蛋白,其中 12 种在 GDM 组中上调,24 种下调。通过 ingenuity 通路分析,脂质代谢是鉴定出的首要类别。通过 Western blot 验证了 3 种随机选择的蛋白,结果与 LC-MS 一致。
正常和 GDM 患者伴肥胖子女的脐静脉血浆蛋白谱存在显著差异。结果表明,多种蛋白质和生物学机制可能与儿童肥胖有关。