Neuroaxonal Dystrophy in Calcium-Independent Phospholipase A(2)beta Deficiency Results from Insufficient Remodeling and Degeneration of Mitochondrial and Presynaptic Membranes

作者：Beck Goichi; Sugiura Yuki; Shinzawa Koei; Kato Shinsuke; Setou Mitsutoshi; Tsujimoto Yoshihide; Sakoda Saburo; Sumi Akamaru Hisae^*

来源：Journal of Neuroscience, 2011, 31(31): 11411-11420.

DOI：10.1523/JNEUROSCI.0345-11.2011

Infantile neuroaxonal dystrophy (INAD) is a fatal neurodegenerative disease characterized by the widespread presence of axonal swellings (spheroids) in the CNS and PNS and is caused by gene abnormality in PLA2G6 [ calcium-independent phospholipase A(2)beta (iPLA(2)beta)], which is essential for remodeling of membrane phospholipids. To clarify the pathomechanism of INAD, we pathologically analyzed the spinal cords and sciatic nerves of iPLA(2)beta knock-out (KO) mice, a model of INAD. At 15 weeks (preclinical stage), periodic acid-Schiff (PAS)-positive granules were frequently observed in proximal axons and the perinuclear space of large neurons, and these were strongly positive for a marker of the mitochondrial outer membrane and negative for a marker of the inner membrane. By 100 weeks (late clinical stage), PAS-positive granules and spheroids had increased significantly in the distal parts of axons, and ultrastructural examination revealed that these granules were, in fact, mitochondria with degenerative inner membranes. Collapse of mitochondria in axons was accompanied by focal disappearance of the cytoskeleton. Partial membrane loss at axon terminals was also evident, accompanied by degenerative membranes in the same areas. Imaging mass spectrometry showed a prominent increase of docosahexaenoic acid-containing phosphatidylcholine in the gray matter, suggesting insufficient membrane remodeling in the presence of iPLA(2)beta deficiency. Prominent axonal degeneration in neuroaxonal dystrophy might be explained by the collapse of abnormal mitochondria after axonal transportation. Insufficient remodeling and degeneration of mitochondrial inner membranes and presynaptic membranes appear to be the cause of the neuroaxonal dystrophy in iPLA(2)beta-KO mice.

• 出版日期2011-8-3