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Investigating Alterations in Caecum Microbiota After Traumatic Brain Injury in Mice
Published on: September 19, 2019
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.
Abstract:
Alterations in gut microbiota are known to affect intestinal inflammation and obesity. Antibiotic treatment can affect weight gain by elimination of histone deacetylase (HDAC) inhibitor-producing microbes, which are anti-inflammatory by augmenting regulatory T (Treg) cells. We asked whether mice that lack HDAC6 and have potent suppressive Treg cells are protected from microbiota-induced accelerated weight gain. We crossed wild-type and HDAC6-deficient mice and subjected the offspring to perinatal penicillin, inducing weight gain via microbiota disturbance. We observed that male HDAC6-deficient mice were not protected and developed profoundly accelerated weight gain. The antibiotic-exposed HDAC6-deficient mice showed a mixed immune phenotype with increased CD4+ and CD8+ T-cell activation yet maintained the enhanced Treg cell-suppressive function phenotype characteristic of HDAC6-deficient mice. 16S rRNA sequencing of mouse fecal samples reveals that their microbiota diverged with time, with HDAC6 deletion altering microbiome composition. On a high-fat diet, HDAC6-deficient mice were depleted in representatives of the S24-7 family and Lactobacillus but enriched with Bacteroides and Parabacteroides; these changes are associated with obesity. Our findings further our understanding of the influence of HDACs on microbiome composition and are important for the development of HDAC6 inhibitors in the treatment of human diseases.-Lieber, A. D., Beier, U. H., Xiao, H., Wilkins, B. J., Jiao, J., Li, X. S., Schugar, R. C., Strauch, C. M., Wang, Z., Brown, J. M., Hazen, S. L., Bokulich, N. A., Ruggles, K. V., Akimova, T., Hancock, W. W., Blaser, M. J. Loss of HDAC6 alters gut microbiota and worsens obesity.
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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