Department of Cardiology, Second Affiliated Hospital of Dalian Medical University, No. 467 Zhongshan Road, Dalian 116000, P.R. China.
Department of Cardiology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.
Exp Anim. 2023 Feb 21;72(1):112-122. doi: 10.1538/expanim.22-0054. Epub 2022 Oct 25.
Pyruvate dehydrogenase complex (PDH) is an important complex of three enzymes that transforms pyruvate into acetyl-CoA, subsequently entering the tricarboxylic acid (TCA) cycle to produce ATP and electron donors. As a key regulator of energy and metabolic homeostasis, PDH is considered a potential therapeutic target of many diseases. On the other hand, the relationship between PDH and obesity is not clear. In this study, peripheral blood of Pdha1Lyz2-Cre and C57BL/6 mice fed a high-fat diet (HFD) was collected and subjected to extensive transcriptome sequencing. Differentially expressed genes (DEGs) were identified. Enrichment of functions and signaling pathways analyses were performed based on Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) database. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to verify the genes selected from RNA sequencing (RNA-seq). Eventually, we found that Pdha1Lyz2-Cre mice were more susceptible to HFD-induced obesity. A total of 302 up-regulated genes and 30 down-regulated genes were screened that were differentially expressed between Pdha1Lyz2-Cre mice fed the HFD and the control groups. Furthermore, we verified that significant transcriptional changes in the genes Sgstm1, Ncoa4, Rraga, Slc3a2, Usp15, Gabarapl2, Wipi1, Sh3glb1, Mtmr3, and Cd36 were consistent with the results obtained from RNA-seq analysis. In summary, this study preliminarily established that there is a close relationship between Pdha1 and obesity and revealed the possible downstream pathways and target genes involved, laying a good foundation for the further study of Pdha1 function in the future.
丙酮酸脱氢酶复合物(PDH)是三种酶的重要复合物,可将丙酮酸转化为乙酰辅酶 A,随后进入三羧酸(TCA)循环产生 ATP 和电子供体。作为能量和代谢稳态的关键调节剂,PDH 被认为是许多疾病的潜在治疗靶点。另一方面,PDH 与肥胖之间的关系尚不清楚。在这项研究中,收集了高脂饮食(HFD)喂养的 Pdha1Lyz2-Cre 和 C57BL/6 小鼠的外周血,并进行了广泛的转录组测序。鉴定差异表达基因(DEGs)。根据基因本体论(GO)和京都基因与基因组百科全书(KEGG)数据库进行功能和信号通路富集分析。使用定量实时聚合酶链反应(qRT-PCR)验证从 RNA 测序(RNA-seq)中选择的基因。最终,我们发现 Pdha1Lyz2-Cre 小鼠更容易受到 HFD 诱导的肥胖影响。筛选出 302 个上调基因和 30 个下调基因,这些基因在 HFD 喂养的 Pdha1Lyz2-Cre 小鼠和对照组之间存在差异表达。此外,我们验证了基因 Sgstm1、Ncoa4、Rraga、Slc3a2、Usp15、Gabarapl2、Wipi1、Sh3glb1、Mtmr3 和 Cd36 的转录显著变化与 RNA-seq 分析结果一致。总之,本研究初步建立了 Pdha1 与肥胖之间存在密切关系,并揭示了可能涉及的下游途径和靶基因,为今后进一步研究 Pdha1 功能奠定了良好基础。