The peripheral-type benzodiazepine receptor is involved in control of Ca(2+)-induced permeability transition pore opening in rat brain mitochondria.

摘要

The peripheral-type benzodiazepine receptor (PBR) is an 18kDa mitochondrial membrane protein with still elusive function in cell death. Here, we studied whether PBR is involved in Ca(2+)-induced permeability transition pore (PTP) opening in isolated rat brain mitochondria (RBM). PTP opening is important in mitochondrial events leading to programmed cell death. Immunoblots revealed a single 18kDa anti-PBR antibody-immunoreactive band in purified RBM. Adenine nucleotide transporter, a key PTP component, was found in the PBR-immunoprecipitate. In isolated intact RBM, addition of a specific anti-PBR antibody [H. Li, Z. Yao, B. Degenhardt, G. Teper, V. Papadopoulos, Cholesterol binding at the cholesterol recognition/interaction amino acid consensus (CRAC) of the peripheral-type benzodiazepine receptor and inhibition of steroidogenesis by an HIV TAT-CRAC peptide, Proc. Natl. Acad. Sci. U.S.A. 98 (2001) 1267-1272] delayed Ca(2+)-induced dissipation of membrane potential (psi(m)) and diminished cyclosporine A-sensitive Ca(2+) efflux, which are both indicative for the suppression of PTP opening. Moreover, anti-PBR antibody caused partial retention of Ca(2+) in the mitochondrial matrix in spite of psi(m) dissipation, and reduced activation of respiratory rate at Ca(2+)-induced PTP opening. A release of pro-apoptotic factors, AIF and cytochrome c, from RBM was shown at threshold Ca(2+) load. Anti-PBR antibody blocked the release of AIF but did not affect the cytochrome c release. Addition of ATP was able to initiate PTP closing, associated with psi(m) restoration and Ca(2+) re-accumulation. At the same time mitochondrial protein phosphorylation (incorporation of (32)P from [gamma-(32)P]ATP) occurred and anti-PBR antibody was able to inhibit phosphorylation of these proteins. The endogenous PBR ligand, protoporphyrin IX, facilitated PTP opening and phosphorylation of the mitochondrial proteins, thus, inducing effects opposite to anti-PBR antibody. This study provides evidence for PBR involvement in PTP opening, controlling the Ca(2+)-induced Ca(2+) efflux, and AIF release from mitochondria, important stages of initiation of programmed cell death.