articleJournal of Biological ChemistryMar 25, 2005HYBRID OA

Properties of the Permeability Transition Pore in Mitochondria Devoid of Cyclophilin D

University of Padua · Vollum Institute · +1 more institution

PubMed
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Abstract

We have studied the properties of the permeability transition pore (PTP) in mitochondria from the liver of mice where the Ppif gene encoding for mitochondrial Cyclophilin D (CyP-D) had been inactivated. Mitochondria from Ppif–/– mice had no CyP-D and displayed a striking desensitization of the PTP to Ca2+, in that pore opening required about twice the Ca2+ load necessary to open the pore in strain-matched, wild-type mitochondria. Mitochondria lacking CyP-D were insensitive to Cyclosporin A (CsA), which increased the Ca2+ retention capacity only in mitochondria from wild-type mice. The PTP response to ubiquinone 0, depolarization, pH, adenine nucleotides, and thiol oxidants was similar in mitochondria from…

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791
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Authors

6

Topics & keywords

Keywords
  • Mitochondrial permeability transition pore
  • Mitochondrion
  • Permeability (electromagnetism)
  • Biophysics
  • Cyclophilin
  • Chemistry
  • Cyclophilin A
  • Cell biology
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