Abstract

Host NOD-like receptor family pyrin domain-containing 6 (NLRP6) regulates innate immune responses and gastrointestinal homeostasis. Its protective role in intestinal colitis and tumorigenesis is dependent on the host microbiome. Host innate immunity and microbial diversity also play a role in the severity of allogeneic immune-mediated gastrointestinal graft-versus-host disease (GVHD), the principal toxicity after allogeneic haematopoietic cell transplantation. Here, we examined the role of host NLRP6 in multiple murine models of allogeneic bone marrow transplantation. In contrast to its role in intestinal colitis, host NLRP6 aggravated gastrointestinal GVHD. The impact of host NLRP6 deficiency in mitigating GVHD was observed regardless of co-housing, antibiotic treatment or colonizing littermate germ-free wild-type and NLRP6-deficient hosts with faecal microbial transplantation from specific pathogen-free wild-type and Nlrp6−/− animals. Chimaera studies were performed to assess the role of NLRP6 expression on host haematopoietic and non-haematopoietic cells. The allogeneic [B6Ly5.2 → Nlrp6−/−] animals demonstrated significantly improved survival compared to the allogeneic [B6Ly5.2 → B6] animals, but did not alter the therapeutic graft-versus-tumour effects after haematopoietic cell transplantation. Our results unveil an unexpected, pathogenic role for host NLRP6 in gastrointestinal GVHD that is independent of variations in the intestinal microbiome and in contrast to its well-appreciated microbiome-dependent protective role in intestinal colitis and tumorigenesis.

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Data availability

The raw sequencing reads have been deposited at the NCBI Short Read Archive under BioProject ID PRJNA491725. Metabolomic data, mass spectral analytical parameters and spectral raw data from the study and metadata have been deposited in the NIH Common Fund’s Data Repository and Coordinating Center under Metabolomics Workbench Project ID PR000728.

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Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Acknowledgements

This work was supported by the National Institutes of Health grants AI-075284 (P.R.) and HL-090775 (P.R.), the American Society of Blood and Marrow Transplantation New Investigator Award (T.T.), the JSPS Postdoctoral Fellowships for Research Abroad (H.F.) and the YASUDA Medical Foundation Grants for Research Abroad (H.F.). This research was supported by work performed by the University of Michigan Microbial Systems Molecular Biology Laboratory.

Author information

Author notes

  1. These authors contributed equally: Tomomi Toubai, Hideaki Fujiwara, Corinne Rossi.

Affiliations

  1. Department of Internal Medicine, Division of Hematology and Oncology, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI, USA

    • Tomomi Toubai
    • , Hideaki Fujiwara
    • , Corinne Rossi
    • , Mary Riwes
    • , Cynthia Zajac
    • , Katherine Oravecz-Wilson
    • , Yaping Sun
    • , Daniel Peltier
    • , Julia Wu
    • , Jiachen Chen
    • , Sergey Seregin
    • , Israel Henig
    • , Stephanie Kim
    • , Stuart Brabbs
    •  & Pavan Reddy
  2. Division of Hematology, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Japan

    • Hiroya Tamaki
    •  & Ikuo Matsuda
  3. Department of Pathology and Laboratory Medicine, Rutgers-Robert Wood Johnson Medical School, New Brunswick, NJ, USA

    • Chen Liu
  4. Division of Nephrology, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI, USA

    • Anna V. Mathew
    • , Jaeman Byun
    •  & Subramaniam Pennathur
  5. Department of Internal Medicine, Division of Hematology and Oncology, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI, USA

    • Grace Chen

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Contributions

T.T. designed and performed the experiments, analysed the data and wrote the paper. H.F., C.R. and M.R. performed the experiments, analysed the data and wrote the paper. H.T. and C.Z. performed the experiments and analysed the data. C.L. performed the experiments and histopathological analysis. A.V.M., J.B., K.O.-W., I.M., S.B., Y.S., D.P., J.W., I.H., S.K., J.C., S.S. and S.P. performed the experiments. G.C. analysed the data, contributed reagents and wrote the paper. P.R. designed the experiments, analysed the data and wrote the paper.

Competing interests

The authors declare no competing interests.

Corresponding authors

Correspondence to Grace Chen or Pavan Reddy.

Supplementary information

  1. Supplementary Information

    Supplementary Figures 1–5.

  2. Reporting Summary

  3. Supplementary Table 1

    A dataset showing the exact P values for all graphs in this manuscript.

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DOI

https://doi.org/10.1038/s41564-019-0373-1