Apoptosis-inducing factor deficiency induces early mitochondrial degeneration in brain followed by progressive Multifocal neuropathology

作者:El Ghouzzi Vincent*; Csaba Zsolt; Olivier Paul; Lelouvier Benjamin; Schwendimann Leslie; Dournaud Pascal; Verney Catherine; Rustin Pierre; Gressens Pierre
来源:Journal of Neuropathology and Experimental Neurology, 2007, 66(9): 838-847.
DOI:10.1097/NEN.0b013e318148b822

摘要

Apoptosis-inducing factor (AIF) deficiency compromises oxidative phosphorylation. Harlequin mice, in which AIF is downregulated, develop a severe mitochondrial complex I (CI) deficiency, suggesting that Harlequin mice may represent a natural model of the most common oxidative phosphorylation disorders. However, the brain phenotype specifically involves the cerebellum, whereas human CI deficiencies often manifest as complex multifocal neuropathologies. To evaluate whether this model can be used as to study CI-deficient disorders, the whole brain of Harlequin mice was investigated during the course of the disease. Neurodegeneration was not restricted to the cerebellum but progressively affected thalamic, striatal, and cortical regions as well. Strong astroglial and microglial activation with extensive vascular proliferation was observed by 4 months of age in thalamic, striatal, and cerebellar nuclei associated with somatosensory-motor pathways. At 2 months of age, degenerating mitochondria were observed in most cells in these structures, even in nondegenerating neurons, a finding that indicates mitochondrial injury is a cause rather than an effect of neuronal cell death. Thus, apoptosis-inducing factor deficiency induces early mitochondrial degeneration, followed by progressive multifocal neuropathology (a phenotype broader than previously described), and resembles some histopathologic features of devastating human neurodegenerative mitochondriopathies associated with CI deficiency.

  • 出版日期2007-9