Insertion of proteolipid protein into oligodendrocyte mitochondria regulates extracellular pH and adenosine triphosphate.

Abstract

Proteolipid protein (PLP) and DM20, the most abundant myelin proteins, are coded by the human PLP1 and non-human Plp1 PLP gene. Mutations in the PLP1 gene cause Pelizaeus-Merzbacher disease (PMD) with duplications of the native PLP1 gene accounting for 70% of PLP1 mutations. Humans with PLP1 duplications and mice with extra Plp1 copies have extensive neuronal degeneration. The mechanism that causes neuronal degeneration is unknown. We show that native PLP traffics to mitochondria when the gene is duplicated in mice and in humans. This report is the first demonstration of a specific cellular defect in brains of PMD patients; it validates rodent models as ideal models to study PMD. Insertion of nuclear-encoded mitochondrial proteins requires specific import pathways; we show that specific cysteine motifs, part of the Mia40/Erv1 mitochondrial import pathway, are present in PLP and are required for its insertion into mitochondria. Insertion of native PLP into mitochondria of transfected cells acidifies media, partially due to increased lactate; it also increases adenosine triphosphate (ATP) in the media. The same abnormalities are found in the extracellular space of mouse brains with extra copies of Plp1. These physiological abnormalities are preventable by mutations in PLP cysteine motifs, a hallmark of the Mia40/Erv1 pathway. Increased extracellular ATP and acidosis lead to neuronal degeneration. Our findings may be the mechanism by which microglia are activated and proinflammatory molecules are upregulated in Plp1 transgenic mice (Tatar et al. (2010) ASN Neuro 2:art:e00043). Manipulation of this metabolic pathway may restore normal metabolism and provide therapy for PMD patients.

• Authors: Sunita Appikatla, Denise Bessert, Icksoo Lee, Maik Hüttemann, Chadwick Mullins, Mallika Somayajulu-Nitu, Fayi Yao, Robert P Skoff
• Journal: Glia (Glia) Vol. 62 Issue 3 Pg. 356-73 (Mar 2014) ISSN: 1098-1136 [Electronic] United States
• PMID: 24382809 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2013 Wiley Periodicals, Inc.

Chemical References

• Myelin Proteolipid Protein
• Nerve Tissue Proteins
• PLP1 protein, human
• Lactic Acid
• Adenosine Triphosphate
• Electron Transport Complex IV

Topics

• Adenosine Triphosphate (metabolism)
• Animals
• Animals, Newborn
• Brain (cytology)
• Cells, Cultured
• Chlorocebus aethiops
• Electron Transport Complex IV (metabolism)
• Extracellular Fluid (metabolism)
• Female
• Gene Expression Regulation (genetics)
• Humans
• Hydrogen-Ion Concentration
• Lactic Acid (metabolism)
• Male
• Mice
• Mice, Inbred C57BL
• Mice, Transgenic
• Middle Aged
• Mitochondria (genetics, metabolism)
• Mutagenesis, Site-Directed
• Mutation (genetics)
• Myelin Proteolipid Protein (genetics, metabolism)
• Nerve Tissue Proteins (metabolism)
• Oligodendroglia (ultrastructure)
• Pelizaeus-Merzbacher Disease (genetics, pathology)