Identification and characterization of T reg–like cells in zebrafish

Author:

Kasheta Melissa1,Painter Corrie A.1,Moore Finola E.2345,Lobbardi Riadh2345,Bryll Alysia1,Freiman Eli1ORCID,Stachura David6,Rogers Arlin B.7,Houvras Yariv8,Langenau David M.2345ORCID,Ceol Craig J.1ORCID

Affiliation:

1. Program in Molecular Medicine and Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA

2. Molecular Pathology Unit, Massachusetts General Hospital, Charlestown, MA

3. Center for Cancer Research, Massachusetts General Hospital, Charlestown, MA

4. Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA

5. Harvard Stem Cell Institute, Cambridge, MA

6. Department of Biological Sciences, California State University, Chico, CA

7. Department of Biomedical Sciences, Cummings School of Veterinary Medicine at Tufts University, North Grafton, MA

8. Departments of Surgery and Medicine, Weill Cornell Medical College, New York, NY

Abstract

Regulatory T (T reg) cells are a specialized sublineage of T lymphocytes that suppress autoreactive T cells. Functional studies of T reg cells in vitro have defined multiple suppression mechanisms, and studies of T reg–deficient humans and mice have made clear the important role that these cells play in preventing autoimmunity. However, many questions remain about how T reg cells act in vivo. Specifically, it is not clear which suppression mechanisms are most important, where T reg cells act, and how they get there. To begin to address these issues, we sought to identify T reg cells in zebrafish, a model system that provides unparalleled advantages in live-cell imaging and high-throughput genetic analyses. Using a FOXP3 orthologue as a marker, we identified CD4-enriched, mature T lymphocytes with properties of T reg cells. Zebrafish mutant for foxp3a displayed excess T lymphocytes, splenomegaly, and a profound inflammatory phenotype that was suppressed by genetic ablation of lymphocytes. This study identifies T reg–like cells in zebrafish, providing both a model to study the normal functions of these cells in vivo and mutants to explore the consequences of their loss.

Funder

Cancer Research Institute

Kimmel Scholar Award

NIH

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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