linc-ADAIN, a human adipose lincRNA, regulates adipogenesis by modulating KLF5 and IL-8 mRNA stability

Cell Rep. 2024 May 28;43(5):114240. doi: 10.1016/j.celrep.2024.114240. Epub 2024 May 14.

Abstract

Adipose tissue remodeling and dysfunction, characterized by elevated inflammation and insulin resistance, play a central role in obesity-related development of type 2 diabetes (T2D) and cardiovascular diseases. Long intergenic non-coding RNAs (lincRNAs) are important regulators of cellular functions. Here, we describe the functions of linc-ADAIN (adipose anti-inflammatory), an adipose lincRNA that is downregulated in white adipose tissue of obese humans. We demonstrate that linc-ADAIN knockdown (KD) increases KLF5 and interleukin-8 (IL-8) mRNA stability and translation by interacting with IGF2BP2. Upregulation of KLF5 and IL-8, via linc-ADAIN KD, leads to an enhanced adipogenic program and adipose tissue inflammation, mirroring the obese state, in vitro and in vivo. KD of linc-ADAIN in human adipose stromal cell (ASC) hTERT adipocytes implanted into mice increases adipocyte size and macrophage infiltration compared to implanted control adipocytes, mimicking hallmark features of obesity-induced adipose tissue remodeling. linc-ADAIN is an anti-inflammatory lincRNA that limits adipose tissue expansion and lipid storage.

Keywords: CP: Metabolism; CP: Molecular biology; HuR; IGF2BP2; IL-8; KLF5; adipogenesis; linc-ADAIN; linc-DMRT2; linc01230; long non-coding RNA; obesity.

MeSH terms

  • Adipocytes / metabolism
  • Adipogenesis* / genetics
  • Adipose Tissue / metabolism
  • Animals
  • Humans
  • Inflammation / genetics
  • Inflammation / metabolism
  • Inflammation / pathology
  • Interleukin-8* / genetics
  • Interleukin-8* / metabolism
  • Kruppel-Like Transcription Factors* / genetics
  • Kruppel-Like Transcription Factors* / metabolism
  • Mice
  • Obesity / genetics
  • Obesity / metabolism
  • Obesity / pathology
  • RNA Stability* / genetics
  • RNA, Long Noncoding* / genetics
  • RNA, Long Noncoding* / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism

Substances

  • IGF2BP2 protein, human
  • Interleukin-8
  • KLF5 protein, human
  • Kruppel-Like Transcription Factors
  • RNA, Long Noncoding
  • RNA, Messenger
  • RNA-Binding Proteins