| Literature DB >> 19075187 |
Xianghong Chen1, Fanqi Bai, Lubomir Sokol, Junmin Zhou, Amy Ren, Jeffrey S Painter, Jinhong Liu, David A Sallman, Y Ann Chen, Jeffrey A Yoder, Julie Y Djeu, Thomas P Loughran, Pearlie K Epling-Burnette, Sheng Wei.
Abstract
Large granular lymphocyte (LGL) leukemia, or LGLL, is characterized by increased numbers of circulating clonal LGL cells in association with neutropenia, anemia, rheumatoid arthritis, and pulmonary artery hypertension (PAH). Emerging evidence suggests that LGLL cells with a CD8(+)CD28(null) phenotype induce these clinical manifestations through direct destruction of normal tissue. Compared with CD8(+)CD28(null) T cells from healthy controls, CD8(+)CD28(null) T cells from LGLL patients have acquired the ability to directly lyse pulmonary artery endothelial cells and human synovial cells. Here, we show that LGLL cells from patients possess enhanced cytotoxic characteristics and express elevated levels of activating natural killer receptors as well as their signaling partners, DAP10 and DAP12. Moreover, downstream targets of DAP10 and DAP12 are constitutively activated in LGLL cells, and expression of dominant-negative DAP10 and DAP12 dramatically reduces their lytic capacity. These are the first results to show that activating NKR-ligand interactions play a critical role in initiating the DAP10 and DAP12 signaling events that lead to enhanced lytic potential of LGLL cells. Results shown suggest that inhibitors of DAP10 and DAP12 or other proteins involved in this signaling pathway will be attractive therapeutic targets for the treatment of LGLL and other autoimmune diseases and syndromes.Entities:
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Year: 2008 PMID: 19075187 PMCID: PMC2665892 DOI: 10.1182/blood-2008-07-168245
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113