Department of Translational Medicine, Federico II University of Naples, Naples, Italy.
URT Genomics of Diabetes, Institute of Experimental Endocrinology and Oncology, National Research Council, Naples, Italy.
FASEB J. 2024 Oct 15;38(19):e70093. doi: 10.1096/fj.202401470R.
The risk of developing type 2 diabetes (T2D) is heterogeneous among individuals with obesity. Functional decline of adipocyte precursor cells (APCs) and accumulation of senescent cells in the subcutaneous adipose tissue contributes to the progression toward T2D. LncRNAs regulate cell senescence and may be implicated in determining this abnormality in APCs. Here, we report that APCs from individuals with obesity show a gradual increase in multiple senescence markers, which worsens in parallel with the progression from normal glucose tolerance (NGT) to impaired glucose tolerance (IGT) or T2D. Transcriptomic analysis identified PANDAR as the top-ranked lncRNA differentially expressed in APCs from individuals with obesity and T2D and non-obese subjects. Q-PCR confirmed PANDAR up-regulation in APCs from individuals with obesity, at progressively increased levels in those who developed, respectively, IGT and T2D. Bisulfite sequencing and luciferase assays revealed that, in parallel with glucose tolerance deterioration, the -1317 CpG at the PANDAR promoter became hypo-methylated in obesity, resulting in enhanced PANDAR induction by p53. PANDAR silencing in senescent APCs from individuals with obesity and T2D caused repression of senescence programs and cell cycle re-entry. PANDAR transcription in white blood cells (WBCs) mirrored that in APCs. Also, individuals with obesity exhibited rescue of PANDAR transcription in WBCs following bariatric surgery, accompanied by enhanced methylation at the regulatory PANDAR -1317 CpG. In conclusion, PANDAR dysregulation is a newly identified mechanism determining the early senescence of APCs from individuals with obesity, which worsens along the progression toward T2D. In the future, PANDAR targeting may represent a valuable strategy to delay this progression.
2 型糖尿病(T2D)的发病风险在肥胖个体中存在异质性。脂肪细胞前体细胞(APCs)功能下降和衰老细胞在皮下脂肪组织中的积累导致向 T2D 的进展。lncRNAs 调节细胞衰老,可能与 APCs 中的这种异常有关。在这里,我们报告肥胖个体的 APCs 显示出多个衰老标志物的逐渐增加,这些标志物的恶化与从正常糖耐量(NGT)到糖耐量受损(IGT)或 T2D 的进展平行。转录组分析确定 PANDAR 是肥胖个体和非肥胖个体的 APCs 中差异表达的排名最高的 lncRNA。Q-PCR 证实肥胖个体的 APCs 中 PANDAR 上调,在分别发展为 IGT 和 T2D 的个体中,其上调水平逐渐增加。亚硫酸氢盐测序和荧光素酶测定显示,随着葡萄糖耐量恶化,PANDAR 启动子上的-1317 CpG 在肥胖中变得低甲基化,导致 p53 增强 PANDAR 的诱导。在肥胖和 T2D 的 APCs 衰老中沉默 PANDAR 导致衰老程序和细胞周期再进入的抑制。肥胖个体的白细胞(WBCs)中 PANDAR 的转录与 APCs 中的转录相匹配。此外,肥胖个体在减肥手术后,WBCs 中的 PANDAR 转录得到挽救,同时在调节 PANDAR-1317 CpG 处的甲基化增强。总之,PANDAR 失调是确定肥胖个体 APCs 早期衰老的一个新发现的机制,这种恶化随着向 T2D 的进展而加剧。将来,针对 PANDAR 的治疗可能代表一种延迟这种进展的有价值的策略。