Amphiphysin 2 (Bin1) and T-Tubule Biogenesis in Muscle

Eunkyung Lee(Howard Hughes Medical Institute), Melissa Marcucci(Howard Hughes Medical Institute), Laurie Daniell(Howard Hughes Medical Institute), Marc Pypaert(Howard Hughes Medical Institute), Ora A. Weisz(University of Pittsburgh), Gian-Carlo Ochoa(Howard Hughes Medical Institute), Khashayar Farsad(Howard Hughes Medical Institute), Markus R. Wenk(Howard Hughes Medical Institute), Pietro De Camilli(Howard Hughes Medical Institute)
Science
August 16, 2002
Cited by 466

Abstract

In striated muscle, the plasma membrane forms tubular invaginations (transverse tubules or T-tubules) that function in depolarization-contraction coupling. Caveolin-3 and amphiphysin were implicated in their biogenesis. Amphiphysin isoforms have a putative role in membrane deformation at endocytic sites. An isoform of amphiphysin 2 concentrated at T-tubules induced tubular plasma membrane invaginations when expressed in nonmuscle cells. This property required exon 10, a phosphoinositide-binding module. In developing myotubes, amphiphysin 2 and caveolin-3 segregated in tubular and vesicular portions of the T-tubule system, respectively. These findings support a role of the bilayer-deforming properties of amphiphysin at T-tubules and, more generally, a physiological role of amphiphysin in membrane deformation.


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