Tbata modulates thymic stromal cell proliferation and thymus function

Author:

Flomerfelt Francis A.1,El Kassar Nahed1,Gurunathan Chandra1,Chua Kevin S.1,League Stacy C.1,Schmitz Sabrina1,Gershon Timothy R.2,Kapoor Veena1,Yan Xiao-Yi1,Schwartz Ronald H.3,Gress Ronald E.1

Affiliation:

1. Experimental Transplantation Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892

2. Department of Neurology, 6109E Neuroscience Research Building, University of North Carolina, Chapel Hill, NC 27599

3. Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, MD 20892

Abstract

Niche availability provided by stromal cells is critical to thymus function. Thymi with diminished function contain fewer stromal cells, whereas thymi with robust function contain proliferating stromal cell populations. Here, we show that the thymus, brain, and testes–associated gene (Tbata; also known as SPATIAL) regulates thymic epithelial cell (TEC) proliferation and thymus size. Tbata is expressed in thymic stromal cells and interacts with the enzyme Uba3, thereby inhibiting the Nedd8 pathway and cell proliferation. Thymi from aged Tbata-deficient mice are larger and contain more dividing TECs than wild-type littermate controls. In addition, thymic reconstitution after bone marrow transplantation occurred more rapidly in Rag2−/−Tbata−/− mice than in Rag2−/−Tbata+/+ littermate controls. These findings suggest that Tbata modulates thymus function by regulating stromal cell proliferation via the Nedd8 pathway.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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