Brown adipocyte activation mediates lipid metabolism through exosomal tRNA-derived fragments

Biochem Biophys Res Commun. 2023 Sep 10:672:128-136. doi: 10.1016/j.bbrc.2023.06.038. Epub 2023 Jun 19.

Abstract

Human obesity is related with intrinsic impairments of adipocyte lipolysis and ectopic lipid accumulation. Small regulatory RNAs, such as tRNA-derived fragments (tRFs) and tRNA halves (tiRNAs), are enriched in exosomes and play a crucial role in lipid metabolism. To determine certain tRFs for lipolysis, brown adipocytes were treated with forskolin. Using tRFs sequencing, 207 different expressed exosomal tRFs were determined. In forskolin samples, 145 downregulated and 62 upregulated tRFs were identified. Further, qRT-PCR validated that three notably upregulated tRFs (tRF-Gly-GCC-007, tRF-Gly-GCC-008, and tRF-Gly-GCC-009) were in accordance with the sequencing result. Target genes of tRFs were involved in positive regulation of protein phosphorylation and cell adhesion process by significantly downregulating UCHL1 expression, which might participate in lipolysis. This study might provide therapeutic targets and potential diagnostic biomarkers for obesity treatment.

Keywords: Brown adipocyte; Exosomes; Forskolin; Lipolysis; Obesity; Transfer RNA fragment.

MeSH terms

  • Adipocytes, Brown* / metabolism
  • Colforsin
  • Humans
  • Lipid Metabolism*
  • Obesity / genetics
  • RNA, Transfer / genetics
  • RNA, Transfer / metabolism

Substances

  • Colforsin
  • RNA, Transfer