Abstract
The retinal pigment epithelium (RPE) and the choriocapillaris are affected early in the retinopathy associated with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency. RPE in culture possesses the machinery needed for mitochondrial fatty acid β-oxidation in vitro. To further elucidate pathogenesis of LCHAD retinopathy, we performed immunohistochemistry of the human eye and brain with antibodies to β-oxidation enzymes. Human eye and brain sections were stained with antibodies to medium-chain (MCAD) and very long-chain acyl-CoA dehydrogenase (VLCAD), short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD), and mitochondrial trifunctional protein (MTP) harboring LCHAD. Antibodies to 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) and cytochrome c oxidase subunit I (COX I) were used as a reference. VLCAD, MTP, MCAD, SCHAD, MHBD, and COX I antibodies labeled most retinal layers and tissues of the human eye actively involved in oxidative metabolism (extraocular and intraocular muscle, the RPE, the corneal endothelium, and the ciliary epithelium). MTP and COX I antibodies labeled the inner segments of photoreceptors. The choriocapillaris was labeled only with SCHAD and MCAD antibodies. In the brain, the choroid plexus and nuclei of the brain stem were most intensely labeled with β-oxidation antibodies, whereas COX I antibodies strongly labeled neurons in several regions of the brain. Mitochondrial fatty acid β-oxidation likely plays a role in ocular energy production in vivo. The RPE rather than the choriocapillaris could be the critical affected cell layer in LCHAD retinopathy. Reduced energy generation in the choroid plexus may contribute to the cerebral edema observed in patients with β-oxidation defects.
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Abbreviations
- COX I:
-
cytochrome C oxidase of the respiratory chain
- LCHAD:
-
long-chain 3-hydroxyacyl-CoA dehydrogenase
- MCAD:
-
medium-chain acyl-CoA dehydrogenase
- MHBD:
-
2-methyl-3-hydroxybutyryl-CoA dehydrogenase
- MTP:
-
mitochondrial trifunctional protein
- RPE:
-
retinal pigment epithelium
- SCHAD:
-
short-chain 3-hydroxyacyl-CoA dehydrogenase
- VLCAD:
-
very long-chain acyl-CoA dehydrogenase
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Supported by Grants from the Arvo and Lea Ylppö Foundation, Espoo, Finland; the Eye and Tissue Bank Foundation, Helsinki, Finland; Mary and Georg C. Ehrnrooth Foundation, Helsinki, Finland; the Finnish Medical Foundation, Helsinki, Finland; and the National Institutes of Health, Bethesda, MD.
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Tyni, T., Paetau, A., Strauss, A. et al. Mitochondrial Fatty Acid β-Oxidation in the Human Eye and Brain: Implications for the Retinopathy of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Pediatr Res 56, 744–750 (2004). https://doi.org/10.1203/01.PDR.0000141967.52759.83
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DOI: https://doi.org/10.1203/01.PDR.0000141967.52759.83
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