Extracellular vesicles derived from lipoaspirate fluid promote fat graft survival

Adipocyte. 2021 Dec;10(1):293-309. doi: 10.1080/21623945.2021.1932355.

Abstract

Extracellular vesicles (EVs) are specific subcellular vesicles released by cells under various environmental conditions. Tumescent liposuction is a commonly used procedure in plastic surgery practice. In the present study, we aimed to extract EVs derived from lipoaspirate fluid (LF-EVs) and characterize them using transmission electron microscopy, nanoparticle tracking analysis, and western blotting. The global profiles of proteins and microRNAs from LF-EVs were identified, strongly suggesting a potential regulatory function of LF-EVs. In addition, we investigated the effects and mechanisms of LF-EVs on fat graft survival. Cell functional tests showed that LF-EVs promoted the proliferation, migration, and tube structure formation of human umbilical vein endothelial cells. LF-EVs also promoted the adipogenic differentiation of adipose tissue-derived stem cells. The results of animal experiments showed that the average weights of fat grafts in the LF-EVs-treated group were significantly higher than those in the control group. Histologically, there was less fibrosis, fewer cysts, and increased fat tissue survival in the LF-EVs group. Further investigations of angiogenic and adipogenic factors revealed that LF-EVs also promoted angiogenesis and exerted a pro-adipogenic effect in vivo. Our findings will help to elucidate the functions of LF-EVs and provide a reference dataset for future translational studies.

Keywords: Extracellular vesicles; adipogenesis; adipose tissue; angiogenesis; fat graft; tumescent liposuction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipogenesis
  • Adipose Tissue / metabolism
  • Adult
  • Animals
  • Body Fluids / metabolism*
  • Extracellular Vesicles / metabolism*
  • Female
  • Graft Survival*
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Lipectomy*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • MicroRNAs / analysis
  • Proteins / analysis
  • Stem Cells / metabolism

Substances

  • MicroRNAs
  • Proteins

Grants and funding

This work was supported by the National Natural Science Foundation of China [grant numbers 81501681 and 81871588]; and the Chinese Association of Plastics and Aesthetics [grant numbers 20200900058 and 20201000109].