Human mesenchymal stem cells treatment improved hepatic lesions and reversed gut microbiome disorder in non-alcoholic steatohepatitis

Aging (Albany NY). 2020 Nov 8;12(21):21660-21673. doi: 10.18632/aging.103962. Epub 2020 Nov 8.

Abstract

Effective therapies for non-alcoholic steatohepatitis (NASH) are urgently needed. We investigated the effect of human mesenchymal stem cells (hMSCs) on the intestinal flora in NASH treatment. We isolated the hMSCs from the umbilical cords and divided male C57BL/6 mice into three groups, namely, chow, methionine-choline-deficient (MCD), and MCD+hMSCs. After collecting the feces and liver of the mice, we evaluated the histological changes in the liver and measured the inflammatory and fibrogenesis cytokines. Fecal microbiome and metabolome were analyzed using 16S rRNA gene sequencing analyses. The hMSCs treatment could alleviate hepatic steatosis, inflammation and fibrosis induced by MCD diet. It could also reverse the microbiome and metabolome disorders in the NASH model. Correlation analysis of the interaction among bacteria amplified the effects of the bacteria in host. In conclusion, hMSCs treatment could improve NASH-related lesions and reverse gut microbiome and metabolome disorder in NASH.

Keywords: human mesenchymal stem cells; intestinal flora; metabolome; methionine–choline-deficient diet; non-alcoholic steatohepatitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteria / metabolism*
  • Cells, Cultured
  • Cellular Microenvironment
  • Disease Models, Animal
  • Dysbiosis
  • Feces / microbiology
  • Fibrosis / metabolism
  • Fibrosis / microbiology
  • Fibrosis / pathology
  • Fibrosis / surgery*
  • Gastrointestinal Microbiome*
  • Host-Pathogen Interactions
  • Intestines / microbiology*
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / metabolism*
  • Metabolome
  • Mice, Inbred C57BL
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Non-alcoholic Fatty Liver Disease / microbiology
  • Non-alcoholic Fatty Liver Disease / pathology
  • Non-alcoholic Fatty Liver Disease / surgery*
  • Phenotype
  • Umbilical Cord / cytology