Investigating central tolerance with reaggregate thymus organ cultures
- PMID: 17876094
- DOI: 10.1007/978-1-59745-395-0_11
Investigating central tolerance with reaggregate thymus organ cultures
Abstract
In the thymus, immature CD4+8+ thymocytes expressing randomly rearranged T-cell receptor alpha- and beta-chain genes undergo positive and negative selection events based on their ability to recognize self-peptide/major histocompatibility complex (MHC) molecules expressed by thymic stromal cells. In vivo analysis of the role of thymic stromal cells during intrathymic selection is made difficult by the cellular complexity of the thymic microenvironment in the steady-state adult thymus, and by the lack of appropriate targeting strategies to manipulate gene expression in particular thymic stromal compartments. We have shown that the thymic microenvironment can be readily manipulated in vitro through the use of reaggregate thymus organ cultures, which allow the preparation of three-dimensional thymus lobes from defined stromal and lymphoid cells. Although other in vitro systems support some aspects of T-cell development, reaggregate thymus organ culture remains the only in vitro system able to support efficient MHC class I and II-mediated thymocyte selection events, and so can be used as an effective tool to study the cellular and molecular regulation of positive and negative selection in the thymus.
Similar articles
-
Reaggregate thymus cultures.J Vis Exp. 2008 Aug 28;(18):905. doi: 10.3791/905. J Vis Exp. 2008. PMID: 19066499 Free PMC article.
-
Preparation of 2-dGuo-treated thymus organ cultures.J Vis Exp. 2008 Aug 28;(18):906. doi: 10.3791/906. J Vis Exp. 2008. PMID: 19066498 Free PMC article.
-
TCR signaling for initiation and completion of thymocyte positive selection has distinct requirements for ligand quality and presenting cell type.J Immunol. 2000 Sep 15;165(6):3015-22. doi: 10.4049/jimmunol.165.6.3015. J Immunol. 2000. PMID: 10975810
-
Thymic T-cell tolerance of neuroendocrine functions: physiology and pathophysiology.Cell Mol Biol (Noisy-le-grand). 2001 Feb;47(1):179-88. Cell Mol Biol (Noisy-le-grand). 2001. PMID: 11292253 Review.
-
Studying T-cell repertoire selection using fetal thymus organ culture.Methods Mol Biol. 2007;380:171-84. doi: 10.1007/978-1-59745-395-0_10. Methods Mol Biol. 2007. PMID: 17876093 Review.
Cited by
-
LKB1 regulates TCR-mediated PLCγ1 activation and thymocyte positive selection.EMBO J. 2011 May 18;30(10):2083-93. doi: 10.1038/emboj.2011.116. Epub 2011 Apr 12. EMBO J. 2011. PMID: 21487392 Free PMC article.
-
FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program.Front Immunol. 2013 Jul 12;4:187. doi: 10.3389/fimmu.2013.00187. eCollection 2013. Front Immunol. 2013. PMID: 23874334 Free PMC article.
-
Isolation and transplantation of different aged murine thymic grafts.J Vis Exp. 2015 May 13;(99):e52709. doi: 10.3791/52709. J Vis Exp. 2015. PMID: 25992870 Free PMC article.
-
Transcriptional control of early T and B cell developmental choices.Annu Rev Immunol. 2014;32:283-321. doi: 10.1146/annurev-immunol-032712-100024. Epub 2014 Jan 22. Annu Rev Immunol. 2014. PMID: 24471430 Free PMC article. Review.
-
Tespa1 is involved in late thymocyte development through the regulation of TCR-mediated signaling.Nat Immunol. 2012 May 6;13(6):560-8. doi: 10.1038/ni.2301. Nat Immunol. 2012. PMID: 22561606
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials