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Double-negative BV8S3 T cells expanded in MRL lpr/lpr lymph nodes conserve TCRBJ gene usage of single-positive BV8S3 T cells.
- Source :
-
Microbiology and immunology [Microbiol Immunol] 1997; Vol. 41 (3), pp. 253-60. - Publication Year :
- 1997
-
Abstract
- Enlarged lymph nodes of mice with lpr mutation consist predominantly of CD4- CD8- (double-negative: DN) T cells. Among them, TCRBV8S3 (V beta 8.3) T cells are overrepresented as compared to those in single-positive (SP) T cells. To address the question of whether the expansion of oligoclonal T cells is responsible for the increase in TCRBV8S3 cells, we examined the TCRBJ gene repertoires of BV8S3 DN and SP T cells from multiple MRL lpr/lpr mice. The BJ repertoires of BV3 (V beta 3), BV8S1 (V beta 8.1) and BV8S2 (V beta 8.2) were studied for comparison with those of BV8S3 T cells. The employed method, which was based on a PCR-ELISA technique, was newly developed and allowed us to make a precise quantitation of TCRBJ gene usage of the multiple lymphocyte samples. The results showed that there were no biases of the BJ gene usage by BV8S3 DN T cells as well as other BV T cells. Furthermore, the BJ gene usage of CD4 and CD8 BV8S3 T cells was conserved by the DN T cells. It is suggested that the BV8S3 DN T cells were not expanded by specific antigens. The expansion may result from aberrant regulation specific to the BV8S3-expressing T cells.
- Subjects :
- Animals
CD4 Antigens genetics
CD8 Antigens genetics
DNA, Complementary genetics
Enzyme-Linked Immunosorbent Assay methods
Female
Flow Cytometry
Gene Rearrangement, T-Lymphocyte
Lymph Nodes cytology
Mice
Mice, Inbred MRL lpr
Polymerase Chain Reaction
Reproducibility of Results
Gene Rearrangement, beta-Chain T-Cell Antigen Receptor
Lupus Erythematosus, Systemic immunology
Lymph Nodes immunology
Receptors, Antigen, T-Cell, alpha-beta genetics
T-Lymphocyte Subsets immunology
Subjects
Details
- Language :
- English
- ISSN :
- 0385-5600
- Volume :
- 41
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Microbiology and immunology
- Publication Type :
- Academic Journal
- Accession number :
- 9130237
- Full Text :
- https://doi.org/10.1111/j.1348-0421.1997.tb01197.x