Résumé
Objective: Migration and proliferation of arterial smooth muscle cells are critical responses during restenosis after balloon angioplasty. We investigated the changes in the expression of Ca2+ channels and dystrophin, two determinants of contraction, after balloon injury of rat aortas. Methods: Proliferation and migration of aortic myocytes were triggered in vivo by the passage of an inflated balloon catheter in the aortas of 12-week-old male Wistar rats. We used the whole-cell patch clamp technique to investigate Ba2+ currents (IBa) through Ca2+ channels in single cells freshly isolated from media and neointima at various times after injury (days 2, 7, 15, 30 and 45). Results: No T-type Ca2+ channel current was recorded in any cell at any time. In contrast, a dihydropyridine (DHP)-sensitive L-type IBawas recorded consistently in the media of intact aorta. After aortic injury, IBa decreased dramatically (at days 2 and 7) but recovered over time to reach normal amplitude on days 30 and 45. In the neointima, IBa was absent on day 15 but also increased gradually over time as observed at days 30 and 45. The use of a specific antibody directed against the L-type Ca2+ channel α1C subunit showed, both by immunostaining and by Western blotting, no expression of the Ca2+ channel protein on day 15. Parallel immunodetection of dystrophin showed that this marker of the contractile phenotype of SMCs was also not detectable at this stage in neointimal cells. Both proteins were re-expressed at days 45 and 63. Balloon injury induces a transient down-regulation of IBa in arterial cells. Conclusions: Cell dedifferentiation and proliferation in vivo abolish the expression of L-type Ca2+ channels and dystrophin in neointimal cells. These changes may be critical in the regulation of Ca2+ homeostasis and, thereby, contraction of the arterial SMCs during restenosis following angioplasty.