Arthritis and rheumatism · 2002
Expression of recombination activating genes 1 and 2 in peripheral B cells of patients with systemic lupus erythematosus.
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Girschick Hermann J, Grammer Amrie C, Nanki Toshihiro, Vazquez Eduardo, Lipsky Peter E
Аннотация
OBJECTIVE: To analyze immunoregulatory abnormalities in patients with systemic lupus erythematosus (SLE) by assessing the expression of messenger RNA (mRNA) for types 1 and 2 recombination activating genes (RAG) in the peripheral blood of patients with active SLE.
METHODS: We examined B cell populations and also individual B cells from patients with SLE for the expression of RAG mRNA.
RESULTS: Analysis of bulk mRNA indicated that RAG1 and RAG2 mRNA were found routinely in peripheral B cells of patients with active SLE, but not in healthy subjects. When assessed on a single-cell basis, there was a 3-fold increase in the frequency of RAG1- and RAG2-expressing B cells in SLE patients compared with healthy subjects. Notably, B cells expressing both RAG1 and RAG2 mRNA expressed only IgD mRNA, but not IgG mRNA. Fifty percent of RAG-expressing B cells also expressed VpreB mRNA, whereas all expressed CD154 mRNA. Phenotypic analysis indicated that RAG-expressing B cells were activated, mature B cells.
CONCLUSION: These results indicate that RAG expression is up-regulated in peripheral IgD+ and VpreB+ B cells of patients with active SLE. These cells may contribute to the immunoregulatory abnormalities in patients with SLE.
METHODS: We examined B cell populations and also individual B cells from patients with SLE for the expression of RAG mRNA.
RESULTS: Analysis of bulk mRNA indicated that RAG1 and RAG2 mRNA were found routinely in peripheral B cells of patients with active SLE, but not in healthy subjects. When assessed on a single-cell basis, there was a 3-fold increase in the frequency of RAG1- and RAG2-expressing B cells in SLE patients compared with healthy subjects. Notably, B cells expressing both RAG1 and RAG2 mRNA expressed only IgD mRNA, but not IgG mRNA. Fifty percent of RAG-expressing B cells also expressed VpreB mRNA, whereas all expressed CD154 mRNA. Phenotypic analysis indicated that RAG-expressing B cells were activated, mature B cells.
CONCLUSION: These results indicate that RAG expression is up-regulated in peripheral IgD+ and VpreB+ B cells of patients with active SLE. These cells may contribute to the immunoregulatory abnormalities in patients with SLE.
Предметные рубрики MeSH
Antigens, CD19B-LymphocytesCD40 LigandDNA NucleotidylexotransferaseDNA-Binding ProteinsGene ExpressionGenes, RAG-1HumansImmunoglobulin DImmunoglobulin GImmunoglobulin Light ChainsImmunoglobulin Light Chains, SurrogateImmunoglobulin lambda-ChainsImmunologic MemoryIn Vitro TechniquesLupus Erythematosus, SystemicMembrane GlycoproteinsNuclear ProteinsPhenotypeRNA, MessengerUp-Regulation