Abstract |
As an H(+)-gated subgroup of the degenerin/epithelial Na(+) channel family, acid-sensing ion channels (ASICs) were reported to be involved in various physiological and pathological processes in neurons. However, little is known about the role of ASICs in the function of dendritic cells (DCs). In this study, we investigated the expression of ASICs in mouse bone marrow-derived DCs and their possible role in the function of DCs. We found that ASIC1, ASIC2, and ASIC3 are expressed in DCs at the mRNA and protein levels, and extracellular acid can evoke ASIC-like currents in DCs. We also demonstrated that acidosis upregulated the expression of CD11c, MHC class II, CD80, and CD86 and enhanced the Ag-presenting ability of DCs via ASICs. Moreover, the effect of acidosis on DCs can be abolished by the nonsteroidal anti-inflammatory drugs ibuprofen and diclofenac. These results suggest that ASICs are involved in the acidosis-mediated effect on DC function.
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Authors | Jing Tong, Wen-Ning Wu, Xiaoling Kong, Peng-Fei Wu, Li Tian, Wenjiao Du, Min Fang, Fang Zheng, Jian-Guo Chen, Zheng Tan, Feili Gong |
Journal | Journal of immunology (Baltimore, Md. : 1950)
(J Immunol)
Vol. 186
Issue 6
Pg. 3686-92
(Mar 15 2011)
ISSN: 1550-6606 [Electronic] United States |
PMID | 21321108
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- ASIC1 protein, mouse
- ASIC2 protein, mouse
- ASIC3 protein, rat
- Acid Sensing Ion Channels
- Asic1 protein, rat
- Nerve Tissue Proteins
- Sodium Channels
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Topics |
- Acid Sensing Ion Channels
- Acidosis
(immunology, metabolism, pathology)
- Animals
- Animals, Newborn
- Cell Differentiation
(immunology)
- Cells, Cultured
- Dendritic Cells
(cytology, immunology, metabolism)
- Extracellular Space
(immunology, metabolism)
- Female
- Hydrogen-Ion Concentration
- Mice
- Mice, Inbred BALB C
- Mice, Inbred C57BL
- Nerve Tissue Proteins
(biosynthesis, physiology)
- Rats
- Rats, Sprague-Dawley
- Sodium Channels
(biosynthesis, physiology)
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