University of Leipzig Medical Center, IFB Adiposity Diseases, University of Leipzig, Leipzig, Germany.
Bioinformatics Group, Department of Computer Science and Interdisciplinary Center for Bioinformatics, University of Leipzig, Leipzig, Germany.
Front Endocrinol (Lausanne). 2020 Mar 26;11:138. doi: 10.3389/fendo.2020.00138. eCollection 2020.
Subcutaneous (sc) and visceral (vis) adipose tissue (AT) contribute to the variability in pathophysiological consequences of obesity and adverse fat distribution. To gain insights into the molecular mechanisms distinguishing vis and sc fat, we compared the transcriptome during differentiation of immortalized adipocytes from murine epididymal (epi) and inguinal (ing) AT. RNA was extracted on different days of adipogenesis (-2, 0, 2, 4, 6, 8) and analyzed using Clariom™ D mouse assays (Affymetrix) covering >214,900 transcripts in >66,100 genes. Transcript Time Course Analysis revealed 137 differentially expressed genes. The top genes with most divergent expression dynamics included developmental genes like , and . According to pathway analysis the majority of the genes were enriched in pathways related to AT development. Finally, in paired samples of human vis and sc AT ( = 63), several of these genes exhibited depot-specific variability in expression which correlated closely with body mass index and/or waist-to-hip ratio. In conclusion, intrinsically programmed differences in gene expression patterns during adipogenesis suggest that fat depot specific regulation of adipogenesis contributes to individual risk of obesity.
皮下(sc)和内脏(vis)脂肪组织(AT)导致肥胖和不良脂肪分布的病理生理后果的可变性。为了深入了解区分 vis 和 sc 脂肪的分子机制,我们比较了来自鼠附睾(epi)和腹股沟(ing)AT 的永生化脂肪细胞在分化过程中的转录组。在脂肪生成的不同天数(-2、0、2、4、6、8)提取 RNA,并使用 Clariom™ D 小鼠检测(Affymetrix)分析,该检测覆盖 >66100 个基因中的 >214900 个转录本。转录时间过程分析显示 137 个差异表达基因。表达动态差异最大的前基因包括发育基因,如 、 和 。根据通路分析,大多数基因富集在与 AT 发育相关的通路中。最后,在人类 vis 和 sc AT 的配对样本中(= 63),这些基因中的几个表现出特定脂肪库的表达变异性,与体重指数和/或腰臀比密切相关。总之,脂肪生成过程中基因表达模式的内在编程差异表明脂肪生成的特定脂肪库调节有助于肥胖的个体风险。