Chandra Amit, Bektik Emre, Randhawa Vinay, Feinberg Mark W
Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Int J Mol Sci. 2025 Aug 22;26(17):8147. doi: 10.3390/ijms26178147.
Endothelial dysfunction underlies several vascular complications, including diabetes and atherosclerosis. However, the underlying role of long non-coding RNAs (lncRNAs) remains poorly understood. This study elucidated the role of lncRNA Gm39822 in regulating endothelial dysfunction under healthy and diabetic conditions. Our data revealed that Gm39822 is enriched and upregulated in non-diabetic endothelial cells when exposed to high glucose or inflammatory cytokines (TNF-α and IL-1β). Gm39822 overexpression promoted the expression of vascular cell adhesion molecule-1 (VCAM-1) and the adhesion of leukocytes in non-diabetic ECs but not in diabetic ECs. Conversely, Gm39822 silencing reduced VCAM1 expression and leukocyte adhesion in non-diabetic ECs and not in diabetic ECs. Gm39822 deficiency reduced the expression of inflammatory mediators (including p-P65, P65, P50, p-P38, P38, P-ERK1/2, and ERK1/2) in non-diabetic ECs. Furthermore, Gm39822 knockdown inhibited the secretion of pro-inflammatory cytokines, including TNF-α, IL-1β, and IL-6, suggesting that Gm39822 regulates EC inflammatory responses. Mechanistically, we identified C1D, a nuclear-enriched corepressor, as an interacting partner of Gm39822 that could play an important role in mediating Gm39822 functions in non-diabetic ECs. Collectively, our results identify a novel lncRNA Gm39822 and provide insights into the molecular mechanisms underlying endothelial dysfunction. These findings highlight Gm39822 as a potential therapeutic target for mitigating vascular complications associated with non-diabetic endothelial dysfunction.
内皮功能障碍是包括糖尿病和动脉粥样硬化在内的多种血管并发症的基础。然而,长链非编码RNA(lncRNA)的潜在作用仍知之甚少。本研究阐明了lncRNA Gm39822在健康和糖尿病条件下调节内皮功能障碍中的作用。我们的数据显示,当暴露于高糖或炎性细胞因子(TNF-α和IL-1β)时,Gm39822在非糖尿病内皮细胞中富集并上调。Gm39822过表达促进了非糖尿病内皮细胞中血管细胞粘附分子-1(VCAM-1)的表达和白细胞的粘附,但在糖尿病内皮细胞中未出现这种情况。相反,Gm39822沉默降低了非糖尿病内皮细胞中VCAM1的表达和白细胞粘附,而在糖尿病内皮细胞中则没有。Gm39822缺陷降低了非糖尿病内皮细胞中炎性介质(包括p-P65、P65、P50、p-P38、P38、P-ERK1/2和ERK1/2)的表达。此外,Gm39822敲低抑制了促炎细胞因子(包括TNF-α、IL-1β和IL-6)的分泌,表明Gm39822调节内皮细胞的炎症反应。从机制上讲,我们确定了一种核富集的共抑制因子C1D是Gm39822的相互作用伙伴,它可能在介导Gm39822在非糖尿病内皮细胞中的功能方面发挥重要作用。总体而言,我们的结果鉴定了一种新型lncRNA Gm39822,并为内皮功能障碍的分子机制提供了见解。这些发现突出了Gm39822作为减轻与非糖尿病内皮功能障碍相关的血管并发症的潜在治疗靶点。