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MicroRNAs Control the Maintenance of Thymic Epithelia and Their Competence for T Lineage Commitment and Thymocyte Selection
Author(s) -
Saulius Žuklys,
C. Mayer,
Saule Zhanybekova,
Heather E. Stefanski,
Gretel Nusspaumer,
Jason Gill,
Thomas Barthlott,
Stéphane Chappaz,
Takeshi Nitta,
James Dooley,
Rubén NogalesCadenas,
Yousuke Takahama,
Daniela Finke,
Adrian Liston,
Bruce R. Blazar,
Alberto Pascual-Montano,
Georg A. Holländer
Publication year - 2012
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1200783
Subject(s) - thymocyte , competence (human resources) , lineage (genetic) , biology , microrna , negative selection , positive selection , selection (genetic algorithm) , microbiology and biotechnology , immunology , genetics , gene , psychology , t cell , social psychology , immune system , computer science , artificial intelligence , genome
Thymic epithelial cells provide unique cues for the lifelong selection and differentiation of a repertoire of functionally diverse T cells. Rendered microRNA (miRNA) deficient, these stromal cells in the mouse lose their capacity to instruct the commitment of hematopoietic precursors to a T cell fate, to effect thymocyte positive selection, and to achieve promiscuous gene expression required for central tolerance induction. Over time, the microenvironment created by miRNA-deficient thymic epithelia assumes the cellular composition and structure of peripheral lymphoid tissue, where thympoiesis fails to be supported. These findings emphasize a global role for miRNA in the maintenance and function of the thymic epithelial cell scaffold and establish a novel mechanism how these cells control peripheral tissue Ag expression to prompt central immunological tolerance.

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