Paneth cell defects in Crohn’s disease patients promote dysbiosis
Ta-Chiang Liu, … , Thaddeus S. Stappenbeck, Nita H. Salzman
Ta-Chiang Liu, … , Thaddeus S. Stappenbeck, Nita H. Salzman
Published June 2, 2016
Citation Information: JCI Insight. 2016;1(8):e86907. https://doi.org/10.1172/jci.insight.86907.
View: Text | PDF
Clinical Medicine Gastroenterology Microbiology

Paneth cell defects in Crohn’s disease patients promote dysbiosis

Abstract

BACKGROUND. Paneth cell dysfunction has been implicated in a subset of Crohn’s disease (CD) patients. We previously stratified clinical outcomes of CD patients by using Paneth cell phenotypes, which we defined by the intracellular distribution of antimicrobial proteins. Animal studies suggest that Paneth cells shape the intestinal microbiome. However, it is unclear whether Paneth cell phenotypes alter the microbiome complexity in CD subjects. Therefore, we analyzed the correlation of Paneth cell phenotypes with mucosal microbiome composition and ileal RNA expression in pediatric CD and noninflammatory bowel disease (non-IBD) patients.

METHODS. Pediatric CD (n = 44) and non-IBD (n = 62) patients aged 4 to 18 were recruited prior to routine endoscopic biopsy. Ileal mucosal samples were analyzed for Paneth cell phenotypes, mucosal microbiome composition, and RNA transcriptome.

RESULTS. The prevalence of abnormal Paneth cells was higher in pediatric versus adult CD cohorts. For pediatric CD patients, those with abnormal Paneth cells showed significant changes in their ileal mucosal microbiome, highlighted by reduced protective microbes and enriched proinflammatory microbes. Ileal transcriptome profiles showed reduced transcripts for genes that control oxidative phosphorylation in CD patients with abnormal Paneth cells. These transcriptional changes in turn were correlated with specific microbiome alterations. In non-IBD patients, a subset contained abnormal Paneth cells. However, this subset was not associated with alterations in the microbiome or host transcriptome.

CONCLUSION. Paneth cell abnormalities in human subjects are associated with mucosal dysbiosis in the context of CD, and these changes are associated with alterations in oxidative phosphorylation, potentially in a feedback loop.

FUNDING. The research was funded by Helmsley Charitable Trust (to T.S. Stappenbeck, R.J. Xavier, and D.P.B. McGovern), Crohn’s and Colitis Foundation of America (to N.H. Salzman, T.S. Stappenbeck, R.J. Xavier, and C. Huttenhower), and Doris Duke Charitable Foundation grant 2014103 (to T.C. Liu).

Authors

Ta-Chiang Liu, Bhaskar Gurram, Megan T. Baldridge, Richard Head, Vy Lam, Chengwei Luo, Yumei Cao, Pippa Simpson, Michael Hayward, Mary L. Holtz, Pavlos Bousounis, Joshua Noe, Diana Lerner, Jose Cabrera, Vincent Biank, Michael Stephens, Curtis Huttenhower, Dermot P.B. McGovern, Ramnik J. Xavier, Thaddeus S. Stappenbeck, Nita H. Salzman

×

Figure 1

High prevalence of Type I Paneth cell phenotype in pediatric Crohn’s disease (CD) patients.

Options: View larger image (or click on image) Download as PowerPoint
High prevalence of Type I Paneth cell phenotype in pediatric Crohn’s dis...
(A) Pediatric CD patients (St. Louis cohort: n = 73; Milwaukee cohort: n = 44) showed significantly higher prevalence of Type I Paneth cell phenotype than adult CD patients (St. Louis cohort: n = 170; Los Angeles cohort: n = 361) (****P < 0.001 by ANOVA). (B) Flow chart of the recruitment and exclusion of the Milwaukee pediatric CD cohort. (C) Representative Paneth cell staining by lysozyme immunofluorescence. Red: lysozyme; blue: DAPI. Dashed circle: intestinal crypts. D0: normal Paneth cells; D1, D3: abnormal Paneth cells. Scale bar: 1 μm.