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  Thymic Medullary Epithelial Cell Differentiation Thymocyte Emigrtion, and Control of Autoimmunity Require Lympho-Epithelial Cross Talk via LTβR

Boehm, T., Scheu, S., Pfeffer, K., & Bleul, C. C. (2003). Thymic Medullary Epithelial Cell Differentiation Thymocyte Emigrtion, and Control of Autoimmunity Require Lympho-Epithelial Cross Talk via LTβR. Journal of Experimental Medicine, 198(5), 757-769. doi:10.1084/jem.20030794.

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 Creators:
Boehm, Thomas1, Author           
Scheu, Stefanie, Author
Pfeffer, Klaus, Author
Bleul, Conrad C.1, Author           
Affiliations:
1Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243647              

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 Abstract: Thymocytes depend on the interaction with thymic epithelial cells for the generation of a diverse, nonautoreactive T cell repertoire. In turn, thymic epithelial cells acquire their three-dimensional cellular organization via instructive signals from developing thymocytes. The nature of these signals has been elusive so far. We show that thymocytes and medullary epithelial cells (MECs) communicate via the lymphotoxin β receptor (LTβR) signaling axis. Normal differentiation of thymic MECs requires LTβR ligand on thymocytes and LTβR together with nuclear factor-κB-inducing kinase (Nik) in thymic epithelial cells. Impaired lympho-epithelial cross talk in the absence of the LTβR causes aberrant differentiation and reduced numbers of thymic MECs, leads to the retention of mature T lymphocytes, and is associated with autoimmune phenomena, suggesting an unexpected role for LTβR signaling in central tolerance induction.

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Language(s): eng - English
 Dates: 2003-09-02
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: 000185155500008
DOI: 10.1084/jem.20030794
 Degree: -

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Title: Journal of Experimental Medicine
Source Genre: Journal
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Publ. Info: Baltimore, Md. : Rockefeller Institute for Medical Research
Pages: - Volume / Issue: 198 (5) Sequence Number: - Start / End Page: 757 - 769 Identifier: ISSN: 0022-1007
CoNE: https://pure.mpg.de/cone/journals/resource/954925413886