Integrins are adhesion receptors capable of transmitting intracellular signals that regulate many different cellular functions. Among integrin-mediated signals, the activation of ion channels can be included. We demonstrated that a long-lasting activation of hERG (human ether-a-go-go-related gene) potassium channels occurs in both human neuroblastoma and leukaemia cells after the activation of the beta1 integrin subunit. This activation is apparently a determining factor inducing neurite extension and osteoclastic differentiation in both the cell types. More recently, we provided evidences that beta1 integrins and hERG channels co-precipitate in both the cell types. Preliminary results suggest that a macromolecular signalling complex indeed occurs between integrins and the hERG1 protein and that hERG channel activity can modulate integrin downstream signalling.

Physical and functional interaction between integrins and hERG potassium channels

DEFILIPPI, Paola;
2004-01-01

Abstract

Integrins are adhesion receptors capable of transmitting intracellular signals that regulate many different cellular functions. Among integrin-mediated signals, the activation of ion channels can be included. We demonstrated that a long-lasting activation of hERG (human ether-a-go-go-related gene) potassium channels occurs in both human neuroblastoma and leukaemia cells after the activation of the beta1 integrin subunit. This activation is apparently a determining factor inducing neurite extension and osteoclastic differentiation in both the cell types. More recently, we provided evidences that beta1 integrins and hERG channels co-precipitate in both the cell types. Preliminary results suggest that a macromolecular signalling complex indeed occurs between integrins and the hERG1 protein and that hERG channel activity can modulate integrin downstream signalling.
2004
32
826
827
http://www.biochemsoctrans.org/bst/032/0826/0320826.pdf
focal adhesion kinase (FAK); hERG potassium channel; integrin; ion channel
ARCANGELI A; BECCHETTI A; CHERUBINI A; CROCIANI O; DEFILIPPI P; GUASTI L; HOFMANN G; PILLOZZI S; OLIVOTTO M; WANKE E.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/38705
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