Cell adhesive sequences in mouse laminin beta1 chain

• Published in: Archives of biochemistry and biophysics Vol. 378; no. 2; pp. 311 - 320
• Main Authors: Nomizu, M, Kuratomi, Y, Ponce, M L, Song, S Y, Miyoshi, K, Otaka, A, Powell, S K, Hoffman, M P, Kleinman, H K, Yamada, Y
• Format: Journal Article
• Language: English
• Published: United States 15.06.2000
• Subjects: Amino Acid Sequence; Animals; Cell Adhesion - drug effects; Cell Adhesion - physiology; Cell Line; Cells, Cultured; Dose-Response Relationship, Drug; Edetic Acid - metabolism; Endothelium, Vascular - metabolism; Fibrinolytic Agents - pharmacology; Heparin - pharmacology; Humans; Laminin - chemistry; Laminin - metabolism; Mice; Models, Biological; Molecular Sequence Data; Peptides - metabolism; Protein Binding; Rats; Sepharose - metabolism; Sequence Homology, Amino Acid; Tumor Cells, Cultured
• ISSN: 0003-9861

Laminin-1, a major component of the basement membrane, consists of three different chains, alpha1, beta1, and gamma1. We sought to identify cell adhesive sequences from the mouse laminin beta1 chain by testing HT-1080 fibrosarcoma and B16-F10 melanoma cells for binding to 187 overlapping synthetic peptides which covered the entire chain. Fourteen peptides showed cell adhesive activities with either peptide-conjugated Sepharose beads or peptide-coated plates or both. Additional cells, including neuronal, endothelial, and salivary gland cells, showed biological responses in a cell type-specific manner. B-7, B-133, and B-160 showed the most potent cell attachment. Cell binding on three peptides (B-34, B-133, and B-160) was inhibited by EDTA. Cell adhesion to 11 of the 12 active peptides was inhibited to varying degrees by heparin. Of the 17 active peptides identified in the laminin beta1 chain in this and other studies, 8 are clustered on the amino terminal globular domain, suggesting a possible important role in cell binding for this domain that may be multifunctional. These data demonstrate that the laminin beta1 chain has multiple active sites for cell adhesion, some of which are cell-type specific.