Starch-activated mouse peritoneal macrophages (STpMAC) plated on plastic demonstrate the adhesive properties typical for activated pMAC: attaching as round cells and, within 15 min, spreading out with marginal membrane ruffles. These attached STpMAC were labeled by lactoperoxidase-catalysed 125I surface iodination, sodium dodecyl-sulfate-lysed, and the lysates electrophoresed on polyacrylamide gels which were examined by autoradiography. The STpMAC morphological phenotype correlates with the labeling of a particular protein (195,000, estimated mol wt). Normal pMAC (NpMAC), from unstimulated mice, do not spread and do not display the 195,000 band. Both pMAC band patterns, including the 195,000 band, are relatively resistant to trypsin digestion, as is pMAC adhesion itself trypsin-resistant. Neither class of pMAC exhibits fibronectin (Cell Adhesion Factor, LETS protein) which is a component in the adhesive matrix of cells forming trypsin-sensitive monolayers. When pMAC are tested against antifibronectin antibody, these cells do not give immunofluorescent staining. In summary, two functions in pMAC adhesion, enzyme resistance and the ability to spread, appear related to molecular properties distinctive for pMAC surface protein.
Article| October 01 1978
Identification of macrophage external membrane proteins and their possible role in cell adhesion.
S R Dienstman
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1978) 79 (1): 263–267.
E Pearlstein, S R Dienstman, V Defendi; Identification of macrophage external membrane proteins and their possible role in cell adhesion.. J Cell Biol 1 October 1978; 79 (1): 263–267. doi: https://doi.org/10.1083/jcb.79.1.263
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