Abstract
Ion-motive ATPase play an essential role in many aspects of cell biology, including mononuclear cell (MNC) functions relevant to chronic inflammation. For example, ouabain, a specific inhibitor of Na+, K+ ATPase, suppresses both T and B cell proliferation but induces synthesis of IL-1. Using a cytochemical assay quantified by microdensitometry, total and ouabain-sensitive ATPase activities have been compared in MNC from rheumatoid and control subjects. The sensitivity of these enzymes to inactivation by thiol-blocking reagents has been studied by preincubation with an impermeant SH blocker p-hydroxymercuriphenylsulphonate (pHMPSA). The results show that rheumatoid MNC have significantly impaired ATPase activity compared to healthy cells and that both total and ouabain-sensitive ATPase activities are readily inhibited by pHMPSA. The depressed ATPase activity in rheumatoid MNC could thus be due to blockade/oxidation of a reactive surface thiol, and could contribute to perpetuation of the chronic inflammatory process in these patients.
Original language | English |
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Pages (from-to) | C107-C109 |
Number of pages | 0 |
Journal | Agents Actions |
Volume | 0 |
Issue number | 0 |
DOIs | |
Publication status | Published - 1993 |
Keywords
- Adenosine Triphosphatases
- Arthritis
- Rheumatoid
- Humans
- Leukocytes
- Mononuclear
- Ouabain
- Phenylmercury Compounds
- Sodium-Potassium-Exchanging ATPase