Loss of HDAC6 alters gut microbiota and worsens obesity

Arnon D Lieber1,2, Ulf H Beier3, Haiyan Xiao3

  • 1Department of Medicine New York University School of Medicine (NYUSM), New York, New York, USA.

Insights

Mice lacking HDAC6 did not gain protection from antibiotic-induced weight gain, and instead experienced accelerated obesity. Loss of HDAC6 significantly altered gut microbiota composition, worsening obesity outcomes.

Area of Science:

  • Microbiology
  • Immunology
  • Metabolic disease

Background:

  • Gut microbiota alterations are linked to intestinal inflammation and obesity.
  • Histone deacetylase (HDAC) inhibitors produced by gut microbes can reduce inflammation by enhancing regulatory T (Treg) cells.
  • HDAC6 deficiency is associated with enhanced Treg cell function.

Purpose of the Study:

  • To investigate if mice lacking HDAC6 are protected from microbiota-induced accelerated weight gain.
  • To understand the impact of HDAC6 deficiency on immune response and gut microbiome composition in the context of obesity.

Main Methods:

  • Crossed wild-type and HDAC6-deficient mice, followed by perinatal penicillin administration to induce microbiota disturbance.
  • Analyzed immune cell phenotypes (CD4+, CD8+, Treg cells) and gut microbiome composition using 16S rRNA sequencing.
  • Assessed weight gain and microbiome changes in mice on a high-fat diet.

Main Results:

  • Male HDAC6-deficient mice exposed to antibiotics showed accelerated weight gain, not protection.
  • These mice exhibited mixed immune phenotypes with increased T-cell activation but maintained Treg cell suppressive function.
  • HDAC6 deletion altered microbiome composition, with depletion of S24-7 and Lactobacillus, and enrichment of Bacteroides and Parabacteroides, associated with obesity.

Conclusions:

  • Loss of HDAC6 does not protect against microbiota-induced weight gain and exacerbates obesity.
  • HDAC6 plays a role in modulating gut microbiota composition and immune responses.
  • Findings highlight the potential of HDAC6 inhibitors for treating obesity and related human diseases.

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