Tissue Iron in Friedreich Ataxia

• Published in: Journal of integrative neuroscience Vol. 23; no. 1; p. 4
• Main Author: Koeppen, Arnulf H
• Format: Journal Article
• Language: English
• Published: Singapore IMR Press 10-01-2024
• Subjects: atrophy; cardiomyopathy; Cytoplasm - metabolism; dorsal root ganglia; ferritin; Ferritins - metabolism; ferroportin; friedreich ataxia; Friedreich Ataxia - metabolism; Friedreich Ataxia - pathology; Humans; iron; Iron - metabolism; mitochondrial ferritin; Neurons - metabolism; ferritin; friedreich ataxia; dorsal root ganglia; atrophy; iron; mitochondrial ferritin; ferroportin; cardiomyopathy
• ISSN: 0219-6352
• DOI: 10.31083/j.jin2301004

Heart, dentate nucleus, and dorsal root ganglia (DRG) are targets of tissue damage in Friedreich ataxia (FA). This report summarizes the histology and histopathology of iron in the main tissues affected by FA. None of the affected anatomical sites reveals an elevation of total iron levels. In the myocardium, a small percentage of fibers shows iron-reactive granular inclusions. The accumulation of larger iron aggregates and fiber invasion cause necrosis and damage to the contractile apparatus. In the dentate nucleus, the principal FA-caused tissue injury is neuronal atrophy and grumose reaction. X-ray fluorescence mapping of iron in the dentate nucleus in FA shows retention of the metal in the center of the collapsed structure. Immunohistochemistry of ferritin, a surrogate marker of tissue iron, confirms strong expression in oligodendrocytes of the efferent white matter of the dentate nucleus and abundance of ferritin-positive microglia in the atrophic gray matter. Iron dysmetabolism in DRG is complex and consists of prominent expression of ferritin in hyperplastic satellite cells and residual nodules, also a loss of the iron export protein ferroportin from the cytoplasm of the remaining DRG nerve cells.