Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2006 Nov;119(3):369-75.
doi: 10.1111/j.1365-2567.2006.02441.x. Epub 2006 Aug 10.

Onset of promiscuous gene expression in murine fetal thymus organ culture

Affiliations

Onset of promiscuous gene expression in murine fetal thymus organ culture

Renato Sousa Cardoso et al. Immunology. 2006 Nov.

Abstract

T-cell differentiation and induction of tolerance to self-antigens occurs mainly in the thymus. Thymic stromal cells, specifically medullary thymic epithelial cells, express a diverse set of genes encoding parenchymal organ-specific proteins. This phenomenon has been termed promiscuous gene expression (PGE) and has been implicated in preventing organ-specific autoimmunity by inducing T-cell tolerance to self antigens. Early thymopoiesis and the critical factors involved in T-cell differentiation can be reproduced in vitro by murine fetal thymus organ culture (FTOC), which mimics the natural thymic microenvironment. To evaluate the occurrence of PGE in FTOC, gene expression profiling during in vitro thymic development in BALB/c mice was performed using a set of nylon cDNA microarrays containing 9216 sequences. The statistical analysis of the microarray data (sam program) revealed the temporal repression and induction of 57 parenchymal and seven lymphoid organ-specific genes. Most of the genes analysed are repressed during early thymic development (15-17 days post-coitum). The expression of the autoimmune regulator (AIRE) gene at 16 days post-coitum marks the onset of PGE. This precedes the induction of parenchymal organ genes during the late developmental phase at 20 days post-coitum. The mechanism of T-cell tolerance induction begins during fetal development and continues into adulthood. Our findings are significant because they show a fine demarcation of PGE onset, which plays a central role in induction of T-cell tolerance.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Differential gene expression during the development of FTOC showing that induction of tissue-specific genes emerges at 20 days. Staging corresponds to development of fetal thymus in culture; 15 days FTOC = 13 days gestation thymus plus 2 days in FTOC.
Figure 2
Figure 2
Semi-quantitative reverse transcription-PCR. Confirmation of ZNF gene as induced at 20 days FTOC (a) and emergence of AIRE gene expression at 16 days FTOC (b).
Figure 3
Figure 3
Representation of tissue/organ system-specific gene expression in 20 days FTOC.
Figure 4
Figure 4
Chromosomal distribution of the repressed and induced genes considering all FTOC development (15–20 days). NF, not found.

Similar articles

Cited by

References

    1. Junta CM, Passos GAS. Emergence of TCRαβ V (D) J recombination and transcription during thymus ontogeny of inbred mouse strains. Mol Cell Biochem. 1998;187:67–72. - PubMed
    1. Macedo C, Junta CM, Passos GAS. Onset of T-cell receptor Vβ8.1 and Dβ2.1, V(D)J recombination during thymus development of inbred mouse strains. Immunol Lett. 1999;69:371–3. - PubMed
    1. Espanhol AR, Macedo C, Junta CM, et al. Gene expression profiling during thymus ontogeny and its association with TRVB8-DB2.1 rearrangements of inbred mouse strains. Mol Cell Biochem. 2003;252:223–8. - PubMed
    1. Espanhol AR, Cardoso RS, Junta CM, Victorero G, Loriod B, Nguyen C, Passos GAS. Large scale gene expression analysis of CBA/J mouse strain fetal thymus using cDNA-array hybridizations. Mol Cell Biochem. 2004;206:65–8. - PubMed
    1. Magalhães DA, Macedo C, Junta CM, et al. Hybridization signatures during thymus ontogeny reveals modulation of genes coding for T-cell signaling proteins. Mol Immunol. 2005;42:1043–8. - PubMed

Publication types

MeSH terms

LinkOut - more resources