CD151 (PETA-3/SFA-1) is a member of the transmembrane 4 superfamily (TM4SF) of cell-surface proteins and is expressed abundantly both on the cell surface and in intracellular membranes by the haemopoietic cell lines M07e, HEL and K562. In the presence of mild detergent (CHAPS), CD151 co-immunoprecipitated with integrin α4β1, α5β1, α6β1 and αIIbβ3. The association of CD151 with α4β1 and α5β1 seemed to be constitutive, as it was not modified by treatment of M07e cells with cytokines that regulate integrin function by ‘inside-out ’ signalling. CD151 also associated with other tetraspans in an apparently cell-type-specific fashion, as defined by its co-precipitation with CD9, CD63 and CD81 from M07e cells, but not from K562 cells, which express similar levels of these proteins. F(ab´)2 fragments of monoclonal antibodies (mAbs) against CD151 caused homotypic adhesion of HEL and K562 cells that was dependent on energy and cytoskeletal integrity and was augmented in the presence of RGDS peptides. The adhesion was not blocked by function-inhibiting mAbs against β1 or β3 integrins, suggesting that cell–cell adhesion was not mediated by the binding of integrin to a cell-associated ligand. Furthermore, mAb CD151 did not affect adhesion of the cells to fibronectin, laminin, collagen or fibrinogen, which are ligands for α4β1, α5β1, α6β1 and αIIbβ3 integrins. Taken together, these results indicate that the ligation of CD151 does not induce the up-regulation of integrin avidity, but might act as a component of integrin signalling complexes.
Transmembrane 4 superfamily protein CD151 (PETA-3) associates with β1 and αIIbβ3 integrins in haemopoietic cell lines and modulates cell–cell adhesion
- Views Icon Views
- PDF LinkPDF
- Share Icon Share
- Cite Icon Cite
Stephen FITTER, Paul M. SINCOCK, Corina N. JOLLIFFE, Leonie K. ASHMAN; Transmembrane 4 superfamily protein CD151 (PETA-3) associates with β1 and αIIbβ3 integrins in haemopoietic cell lines and modulates cell–cell adhesion. Biochem J 15 February 1999; 338 (1): 61–70. doi: https://doi.org/10.1042/bj3380061
Download citation file: