The peripheral-type benzodiazepine receptor is involved in control of Ca²⁺-induced permeability transition pore opening in rat brain mitochondria

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• 作者：Tamara Azarashvili ; Dmitry Grachev ; Olga Krestinina ; Youri Evtodienko ; Igor Yurkov ; Vassilios Papadopoulos ; Georg Reiser
• 关键词：Brain mitochondria ; Calcium transport ; Permeability transition pore ; Apoptosis-inducing factor ; Phosphoproteins ; PBR ; Anti-PBR antibodies ; PBR ligands
• 刊名：Cell Calcium
• 出版年：2007
• 出版时间：July 2007
• 年：2007
• 卷：42
• 期：1
• 页码：27-39
• 全文大小：702 K

文摘

The peripheral-type benzodiazepine receptor (PBR) is an 18 kDa mitochondrial membrane protein with still elusive function in cell death. Here, we studied whether PBR is involved in Ca²⁺-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 18 kDa 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 Ca²⁺-induced dissipation of membrane potential (ψ_m) and diminished cyclosporine A-sensitive Ca²⁺ efflux, which are both indicative for the suppression of PTP opening. Moreover, anti-PBR antibody caused partial retention of Ca²⁺ in the mitochondrial matrix in spite of ψ_m dissipation, and reduced activation of respiratory rate at Ca²⁺-induced PTP opening. A release of pro-apoptotic factors, AIF and cytochrome c, from RBM was shown at threshold Ca²⁺ 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 ψ_m restoration and Ca²⁺ re-accumulation. At the same time mitochondrial protein phosphorylation (incorporation of ³²P from [γ-³²P]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 Ca²⁺-induced Ca²⁺ efflux, and AIF release from mitochondria, important stages of initiation of programmed cell death.