Both translocon and a cation channel are involved in the passive Ca2+ leak from the endoplasmic reticulum: a mechanistic study on rat liver microsomes

Abstract

Steady-state levels of calcium ions in endoplasmic reticulum reflect a balance between active inward transport, mediated by MgATP-dependent Ca(2+) pumps, and passive backflux of the ions, through putative "leak channels". We have investigated the efflux of Ca(2+) from rat liver microsomal vesicles, passively pre-equilibrated in the presence radiolabelled Ca(2+). Similarly, we have also evaluated the efflux of a low-Mwt uncharged compound, i.e., sucrose. The results show that two major passive Ca(2+) efflux pathways exist. One appeared to involve the translocon pore, since it was stimulated by the translocon opener puromycin, and also allowed the passage of sucrose. Putative channels likely mediated the other one, since it required counter ion influx and was inhibited by Gd(3+) and La(3+). The latter pathway did not appear to involve inactive Ca(2+) pumps, Bcl2 proteins, or known channels, such as the InsP3 and ryanodine receptors. While sucrose efflux was highly represented in a rough microsomal subfraction--enriched in the translocon component Sec61alpha--the efflux of Ca(2+) was represented both in smooth and in rough microsomes. We conclude that the passive efflux of Ca(2+) from the (liver) ER could be mediated by both the translocon pore and putative Ca(2+) leak channels. However, the relative role of these Ca(2+) efflux pathways in the intact cell as well as the molecular nature of the Ca(2+) leak channel(s) remain to be clarified.