Abstract

p42IP4 is a brain-specific protein also called centaurin-α1. This protein specifically recognizes two second messengers, the membrane lipid PtdIns (3,4,5)P3 and the soluble inositol phosphate Ins(1,3,4,5)P4. Previously, expression of p42IP4 protein in non-neuronal CHO cells stably transfected with pcDNA-p42IP4 was shown in cytosol, membranes and nucleus. The membrane fraction in that study also contained mitochondria. The yeast protein Gcs1p, which is structurally and functionally related to p42IP4, is localized in mitochondria and is involved in maintenance of mitochondrial morphology. The program PSORT II had predicted a high probability for mitochondrial localization of p42IP4. Therefore, localization of p42IP4 in mitochondria was suggested. We show here for the first time that p42IP4 is localized in mitochondria, isolated from cells transfected with p42IP4, CHO cells and mouse neuroblastoma (N2a) cells. In CHO cells, p42IP4 is localized predominantly in the intermembrane space side of the mitochondrial inner membrane. p42IP4 is also found in mitochondria isolated from rat brain. Previously, 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNP) has been shown to be associated with mitochondria, but the exact role of CNP in mitochondria is still obscure. We show the localization of CNP in both mitochondrial membrane fractions by sub-fractionation of rat brain mitochondria (RBM). We additionally found interaction of p42IP4 with CNP in RBM by pull-down binding assay and by immunoprecipitation. Cellular Ca2+ signals are crucial in the control of most physiological processes, cell injury and programmed cell death. In neurons, mitochondria dampen changes in cytosolic Ca2+ loads and sustain cellular Ca2+ homeostasis that is required for normal neuronal function. However, mitochondria take up a limited amount of calcium up to a certain threshold. Accumulation of Ca2+ above this threshold leads to increased permeability of the inner mitochondrial membrane due to formation of a unselective pore at the contact site between outer and inner membranes. Since permeability transition pore (PTP) opening is important in mitochondrial events leading to cell death, we studied whether p42IP4 is involved in Ca2+-induced Ca2+ release and consequently PTP. We determined the Ca2+capacity and lag-phase for PTP opening in mitochondria isolated from p42IP4-transfected and from control N2a cells. Overexpression of p42IP4 led to significant decrease of these functional mitochondrial Ca2+ parameters. Thus, we suggest that due to involvement in the regulation of Ca2+ transport in mitochondria, p42IP4, destabilizes mitochondria by promoting Ca2+-induced PTP opening.

Highlights

  • 12th Joint Meeting of the Signal Transduction Society (STS)

  • We show here for the first time that p42IP4 is localized in mitochondria, isolated from cells transfected with p42IP4, CHO cells and mouse neuroblastoma (N2a) cells

  • In CHO cells, p42IP4 is localized predominantly in the intermembrane space side of the mitochondrial inner membrane. p42IP4 is found in mitochondria isolated from rat brain

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Summary

Introduction

12th Joint Meeting of the Signal Transduction Society (STS). Signal Transduction: Receptors, Mediators and Genes Frank Entschladen, Karlheinz Friedrich, Ralf Hass and Ottmar Janssen Meeting abstracts – A single PDF containing all abstracts in this Supplement is available here. . The neuron-specific protein, p42IP4 (Centaurin-α1) is localized in mitochondria, interacts with 2',3'-cyclic nucleotide 3'-phosphodiesterase and is involved in regulation and control of mitochondrial Ca2+ * Corresponding author from 12th Joint Meeting of the Signal Transduction Society (STS). Signal Transduction: Receptors, Mediators and Genes Weimar, Germany.

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