Abstract

We tested the hypothesis that increased Sarcoplasmic reticulum (SR) Ca content ([Ca](SRT)) in phospholamban knockout mice (PLB-KO) is because of increased SR Ca pump efficiency defined by the steady-state SR [Ca] gradient. The time course of thapsigargin-sensitive ATP-dependent (45)Ca influx into and efflux out of cardiac SR vesicles from PLB-KO and wild-type (WT) mice was measured at 100 nm free [Ca]. We found that PLB decreased the initial SR Ca uptake rate (0.13 versus 0.31 nmol/mg/s) and decreased steady-state (45)Ca content (0.9 versus 4.1 nmol/mg protein). Furthermore, at similar total SR [Ca], the pump-mediated Ca efflux rate was higher in WT (0.065 versus 0.037 nmol/mg/s). The pump-independent leak rate constant (k(leak)) was also measured at 100 nm free [Ca]. The results indicate that k(leak) was < 1% of pump-mediated backflux and was not different among nonpentameric mutant PLB (PLB-C41F), WT pentameric PLB (same expression level), and PLB-KO. Therefore differences in passive SR Ca leak cannot be the cause of the higher thapsigargin-sensitive Ca efflux from the WT membranes. We conclude that the decreased total SR [Ca] in WT mice is caused by decreased SR Ca influx rate, an increased Ca-pump backflux, and unaltered leak. Based upon both thermodynamic and kinetic analysis, we conclude that PLB decreases the energetic efficiency of the SR Ca pump.

Highlights

  • Backflux is a unidirectional flux that results from reversal of the Sarcoplasmic reticulum (SR) Ca pump in the forward mode

  • In this report we measure forward and reverse Ca pump flux and pump-independent leak in SR vesicles from wild-type (WT) mice, phospholamban knockout mice (PLB-KO), and mice that express equal amounts of either wild-type PLB (PLB-70) or nonpentamer-forming mutant PLB (PLB-C41F) upon a knockout background

  • We have provided the following new information: 1) passive leak from the SR with RyR blocked is small relative to backflux through the Ca pump, 2) passive leak from SR membranes is not PLB-dependent, 3) the efficiency of the Ca pump is decreased in the presence of PLB, and [4] PLB regulates this pump efficiency by decelerating influx while accelerating backflux through the SR Ca pump

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Summary

Introduction

Backflux is a unidirectional flux that results from reversal of the SR Ca pump in the forward mode. It is well established that PLB inhibits the forward mode of SR Ca transport by increasing the forward KCa (KCa-f) to higher [Ca], the effects of PLB on reverse SR Ca-ATPase and KCa (KCa-r) are unknown. This becomes an important issue, especially in the case where the Ca pump approaches thermodynamic equilibrium, as may be the case in intact myocytes under some conditions [9]. In this report we measure forward and reverse Ca pump flux and pump-independent leak in SR vesicles from wild-type (WT) mice, phospholamban knockout mice (PLB-KO), and mice that express equal amounts of either wild-type PLB (PLB-70) or nonpentamer-forming mutant PLB (PLB-C41F) upon a knockout background. The data in WT, PLB-KO, and PLB-70 membranes all support this hypothesis

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