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ABSTRACT: Objective
To define the pathogenesis of bone marrow (BM) involvement in systemic lupus erythematosus (SLE).Methods
Tumor necrosis factor α (TNFα) levels, cell death, and cellular damage in BM from SLE patients, controls, and mice with pristane-induced lupus were analyzed using a morphometric technique and immunohistochemistry. The pathogenesis of BM abnormalities was studied in wild-type (WT), TNFα(-/-) , Toll-like receptor-deficient (TLR-7(-/-) ), interferon (IFN)-α/β/ω receptor-knockout (IFNAR(-/-) ), and B cell-deficient (μmt) mice treated with pristane. Flow cytometry was used to examine TNFα production (by intracellular staining) and plasma cell/plasmablast development. CXCL12 expression was determined by quantitative polymerase chain reaction.Results
BM from S
SUBMITTER: Zhuang H
PROVIDER: S-EPMC3990233 | biostudies-literature | 2014 Jan
REPOSITORIES: biostudies-literature