TY - JOUR
T1 - The stromal gene encoding the CD274 antigen as a genetic modifier controlling survival of mice with γ-radiation-induced T-cell lymphoblastic lymphomas
AU - Santos, J.
AU - González-Sánchez, L.
AU - Villa-Morales, M.
AU - Ors, I.
AU - López-Nieva, P.
AU - Vaquero, C.
AU - González-Gugel, E.
AU - Fernández-Navarro, P.
AU - Roncero, A. M.
AU - Guenet, J. L.
AU - Montagutelli, X.
AU - Fernández-Piqueras, J.
N1 - Funding Information:
This work was supported by the European Commission contract number FI6R-CT2003-508842 to JS and by the Spanish Ministry of Education and Science contract number SAF-2006-09437 and SAF2009-11426 to JFP. We thank Arturo Morales for the critical reading of the paper.
PY - 2010/9/23
Y1 - 2010/9/23
N2 - Using an inter-specific subcongenic strain, Nested Recombinant Haplotype 3 (NRH3), generated between two mouse strains showing extreme differences in γ-radiation-induced thymic lymphoma susceptibility (SEG/Pas and C57BL/6J), we have identified a critical region on chromosome 19 that regulates survival of mice suffering from T-cell lymphoblastic lymphomas. Mapped on this region, the gene encoding the Cd274 ligand is able to trigger an inhibitory effect that modulates T-cell receptor (TCR) signalling and affects thymocyte maturation. Interestingly, this gene shows differential expression between thymic stromal cells from both strains in early response to a single sublethal γ-ray dose, but is inhibited in T-cell lymphoblastic lymphomas. Furthermore, we have identified several polymorphisms in the complementary DNA sequence of this gene that affect the affinity for its Cd279 receptor and are able to induce a differential rate of thymocyte apoptosis. Taken together, our data are consistent with Cd274 acting as a genetic modifier that influences the survival of γ-radiation-induced T-cell lymphoma-bearing mice. The data similarly support the idea of a co-evolution of tumour cells and associated stromal cells to generate a favourable microenvironment for T-cell lymphoma growth.
AB - Using an inter-specific subcongenic strain, Nested Recombinant Haplotype 3 (NRH3), generated between two mouse strains showing extreme differences in γ-radiation-induced thymic lymphoma susceptibility (SEG/Pas and C57BL/6J), we have identified a critical region on chromosome 19 that regulates survival of mice suffering from T-cell lymphoblastic lymphomas. Mapped on this region, the gene encoding the Cd274 ligand is able to trigger an inhibitory effect that modulates T-cell receptor (TCR) signalling and affects thymocyte maturation. Interestingly, this gene shows differential expression between thymic stromal cells from both strains in early response to a single sublethal γ-ray dose, but is inhibited in T-cell lymphoblastic lymphomas. Furthermore, we have identified several polymorphisms in the complementary DNA sequence of this gene that affect the affinity for its Cd279 receptor and are able to induce a differential rate of thymocyte apoptosis. Taken together, our data are consistent with Cd274 acting as a genetic modifier that influences the survival of γ-radiation-induced T-cell lymphoma-bearing mice. The data similarly support the idea of a co-evolution of tumour cells and associated stromal cells to generate a favourable microenvironment for T-cell lymphoma growth.
KW - Cd274 gene
KW - T-cell lymphoblastic lymphoma
KW - g-irradiation
KW - survival
KW - thymus stroma
UR - http://www.scopus.com/inward/record.url?scp=77957124165&partnerID=8YFLogxK
U2 - 10.1038/onc.2010.280
DO - 10.1038/onc.2010.280
M3 - Article
C2 - 20639904
AN - SCOPUS:77957124165
SN - 0950-9232
VL - 29
SP - 5265
EP - 5273
JO - Oncogene
JF - Oncogene
IS - 38
ER -