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Whole-cell currents in macrophages: II. Alveolar macrophages
D J Nelson1, B Jow, K J Popovich
1Department of Medicine, University of Chicago, Illinois 60637.
The Journal of Membrane Biology
|July 1, 1990
Summary
Human alveolar macrophages (HAMs) express an inactivating outward potassium current (IA) significantly more often than human monocyte-derived macrophages (HMDMs). This difference in IA expression may impact macrophage immune functions.
Area of Science:
- Immunology
- Cell Physiology
- Ion Channel Research
Background:
- Outwardly rectifying K+ conductance is known in murine macrophages but is rare in human monocyte-derived macrophages (HMDMs).
- Human alveolar macrophages (HAMs) are a primary immune cell population in the lung and a readily available source of human tissue macrophages.
Purpose of the Study:
- To compare the expression of an inactivating outward potassium current (IA) between in vitro differentiated HMDMs and ex vivo isolated HAMs.
- To characterize the properties of IA in both macrophage types.
Main Methods:
- Whole-cell patch-clamp recordings were performed on HMDMs cultured for various durations and on HAMs obtained from bronchoalveolar lavage.
- Ionic currents were analyzed for voltage dependence, ion selectivity, and sensitivity to 4-aminopyridine (4-AP).
Main Results:
- IA was observed in only 5% of HMDMs (49/974 cells) but in 50% of HAMs (160/26 donors).
- The IA current in both cell types was K+ selective, 4-AP sensitive, and showed weakly voltage-dependent inactivation with a recovery time constant of ~30 sec.
- Current inactivation kinetics were dependent on external K+ concentration, and activation/inactivation occurred at specific voltage potentials.
Conclusions:
- HAMs exhibit a significantly higher frequency of IA expression compared to HMDMs.
- The presence of IA may influence mononuclear phagocyte functions such as chemotaxis, phagocytosis, and tumoricidal activity.