MicroRNA-140 is not involved in sepsis-induced muscle atrophy

Am J Physiol Cell Physiol. 2023 Aug 1;325(2):C509-C518. doi: 10.1152/ajpcell.00157.2023. Epub 2023 Jul 24.

Abstract

Sepsis is a life-threatening inflammatory response to infection, often accompanied by skeletal muscle atrophy. A previous study demonstrated that the administration of microRNA-140 (miR-140) attenuated lipopolysaccharide (LPS)-induced muscle atrophy, whereas miR-140 knockdown with siRNA promoted atrophy. Therefore, we investigated whether miR-140 is involved in LPS-induced muscle atrophy using a genetic model, miR-140-/- mice. We found that a single injection of LPS induced atrophy both in slow-twitch and fast-twitch muscles. The muscle weights and fiber cross-sectional areas were significantly reduced in both the wild-type (WT) and miR-140-/- mice, with no difference between genotypes. The expression of several proteolysis markers, muscle-specific RING-finger 1 (MuRF1) and MAFbx/atrogin-1, increased in both groups after LPS injection. The ubiquitinated proteins in the miR-140-/- mice were similar to those in the WT mice. Therefore, the deletion of miR-140 did not affect LPS-induced muscle atrophy.NEW & NOTEWORTHY We used miR-140-/- mice to determine the function of miR-140 in LPS-induced skeletal muscle atrophy. To our knowledge, this study is the first to examine slow-twitch muscles in LPS-induced muscle wasting after miR-140 manipulation.

Keywords: apoptosis; muscle wasting; noncoding RNA; proteolysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Lipopolysaccharides
  • Mice
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Muscle, Skeletal / metabolism
  • Muscular Atrophy / metabolism
  • Sepsis* / complications
  • Sepsis* / genetics
  • Sepsis* / metabolism

Substances

  • Lipopolysaccharides
  • MicroRNAs
  • MIRN140 microRNA, mouse

Associated data

  • figshare/10.6084/m9.figshare.23589792.v1