Surface charge of resident, elicited, and activated mouse peritoneal macrophages
The surface charpa of resident, thioglycollate‐elicited, and Trypanosoma cruzi‐ectivated mouse peritoneal macrophages was analyzed using cell electrophoresis. AN macrophages had a net negative surface charge. Activated macrophages had a lower zeta potential and a higher isoelectrophoretic point than...
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Published in | Journal of leukocyte biology Vol. 41; no. 2; pp. 143 - 149 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Society for Leukocyte Biology
01.02.1987
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Subjects | |
Online Access | Get full text |
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Summary: | The surface charpa of resident, thioglycollate‐elicited, and Trypanosoma cruzi‐ectivated mouse peritoneal macrophages was analyzed using cell electrophoresis. AN macrophages had a net negative surface charge. Activated macrophages had a lower zeta potential and a higher isoelectrophoretic point than resident and elicited macrophages. The populations of resident, elicited, and activated macrophages were heterogeneous in terms of surface charge. The analysis of the effect of the pH of the solution in which the macrophages were suspended on their cellular electrophoretic mobility (EPM) indicated that their surface contained both positively and negatively charged dissociating groups. The contribution of sialic acid residuos to the surface change was determined by analyzing the effect of neuraminidase treatment on the EPM of the cells. Activated mecrophages possessed more sialic add residuos exposed on their surface, and sensitive to the neuraminidase from Clostridium perfrigens, than resident and elicited macrophages. Treatment of the cells with the neuraminidase from Vibrio cholerae, however, reduced the surface charge of all macrophages in about the same extent. Macrophages had their mean EPM reduced when Incubated in the presence of Ca++, suggesting that some cell surface anionogenic sites have Ca++‐binding capacity. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0741-5400 1938-3673 |
DOI: | 10.1002/jlb.41.2.143 |