circLRP6 regulates high glucose‐induced proliferation, oxidative stress, ECM accumulation, and inflammation in mesangial cells

• Published in: Journal of cellular physiology 2019-11, Vol.234 (11), p.21249-21259
• Main Authors: Chen, Bin, Li, Yanhua, Liu, Yang, Xu, Zhonggao
• Format: Article
• Language: English
• Subjects: Accumulation; Binding; Cell proliferation; circLRP6; Deoxyribonucleic acid; Diabetes mellitus; Diabetic nephropathy; DNA; Extracellular matrix; Gene expression; Gene regulation; Glucose; HMGB1; HMGB1 protein; Hyperglycemia; Inflammation; Mesangial cells; miRNA; miR‐205; mRNA; Nephropathy; Nuclear transport; Oxidative stress; Pathogenesis; Phosphorylation; Signal transduction; TLR4 protein; TLR4/NF‐κB pathway; Toll-like receptors; Translocation
• ISSN: 0021-9541; 1097-4652
• DOI: 10.1002/jcp.28730

Aberrant regulation in mesangial cell proliferation, extracellular matrix (ECM) accumulation, oxidative stress, and inflammation under hyperglycemic condition contributes significantly to the occurrence and development of diabetic nephropathy (DN). However, the mechanisms underlying the hyperglycemia‐induced dysregulations have not been clearly elucidated. Here, we reported that high mobility group box 1 (HMGB1) was highly elevated in high glucose (HG)‐treated mesangial cells, and induced the phosphorylation, nuclear translocation, and DNA binding activity of NF‐κB via toll‐like receptor 4 (TLR4). Function assays showed that inhibition of HMGB1 mitigated HG‐induced proliferation, oxidative stress, ECM accumulation, and inflammation in mesangial cells via TLR4/NF‐κB pathway. Increasing evidence has shown that circRNA, a large class of noncoding RNAs, functions by binding with miRNAs and terminating regulation of their target genes. We further investigated whether HMGB1 is involved in circRNA–miRNA–mRNA regulatory network. First, HMGB1 was identified and confirmed to be the target of miR‐205, and miR‐205 played a protective role against HG‐induced cell injure via targeting HMGB1. Then circLRP6 was found to be upregulated in HG‐treated mesangial cells, and regulate HG‐induced mesangial cell injure via sponging miR‐205. Besides, overexpression of miR‐205 or knockdown of circLRP6 inhibited the NF‐κB signaling pathway. Collectively, these data suggest that circLRP6 regulates HG‐induced proliferation, oxidative stress, ECM accumulation, and inflammation in mesangial cells via sponging miR‐205, upregulating HMGB1 and activating TLR4/NF‐κB pathway. These findings provide a better understanding for the pathogenesis of DN. 1. Inhibition of high mobility group box 1 (HMGB1) mitigated high glucose (HG)‐induced proliferation, oxidative stress, extracellular matrix (ECM) accumulation, and inflammation in mesangial cells via TLR4/NF‐κB pathway. 2. HMGB1 was identified and confirmed to be the target of miR‐205, and miR‐205 played a protective role against HG‐induced cell injure via targeting HMGB1. 3. circLRP6 regulates HG‐induced proliferation, oxidative stress, ECM accumulation, and inflammation in mesangial cells via sponging miR‐205, upregulating HMGB1 and activating TLR4/NF‐κB pathway.