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Laminin inhibits the adhesion of a murine tumor of macrophage origin
Authors:Raffaella Giavazzi   Lance Liotta  Ian Hart
Affiliation:1. Cancer Metastasis and Treatment Laboratory, NCI-Frederick Cancer Research Facility, Frederick, MD 21701 USA;2. Laboratory of Pathophysiology, National Cancer Institute NIH, Bethesda, MD 20205, USA
Abstract:The adhesive behavior of the M5076 reticulum cell sarcoma, a highly metastatic murine tumor of macrophage origin, was investigated in vitro both in the presence and in the absence of purified exogeneous laminin. Although laminin enhanced the adhesion of other murine cell lines to collagen-coated and plastic surfaces, it reduced the attachment to both substrates of M5076 cells, peritoneal macrophages and the macrophage cell line WEHI-3. Thus, the inhibition appeared to be related to the macrophage nature of the M5076 tumor. The effects of laminin were reversible and did not cause loss of viability or functional capacity of the M5076 cells. Laminin appeared to exert this inhibitory effect by binding to the substrates rather than binding to the cells. These studies indicate that laminin, a glycoprotein from the basement membrane, may either stimulate or inhibit cell attachment, depending on the type of cell.
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