Oligodendroglial differentiation induces mitochondrial genes and inhibition of mitochondrial function represses oligodendroglial differentiation

Mitochondrion

Volumn 10, Issue 2, 2010, Pages 143-150

  Schoenfeld, Robert ^a   Wong, Alice ^a   Silva, Jillian ^a   Li, Ming ^a   Itoh, Aki ^b   Horiuchi, Makoto ^b   Itoh, Takayuki ^b   Pleasure, David ^b   Cortopassi, Gino ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cholesterol; Mitochondria; Myelination; Oligodendroglia; Rotenone

Indexed keywords

2',3' CYCLIC NUCLEOTIDE 3' PHOSPHODIESTERASE; ACETYL COENZYME A; ADENOSINE TRIPHOSPHATE; CHOLESTEROL; MITOCHONDRIAL DNA; MYELIN; MYELIN BASIC PROTEIN; ROTENONE;

ANIMAL CELL; ARTICLE; CELL DIFFERENTIATION; CELL FUNCTION; CELL VIABILITY; CONTROLLED STUDY; ENZYME SYNTHESIS; GENE AMPLIFICATION; GENE EXPRESSION; HUMAN; HUMAN CELL; HUMAN VERSUS ANIMAL COMPARISON; INHIBITION KINETICS; MITOCHONDRIAL GENE; MITOCHONDRIAL GENETICS; MYELINATION; NONHUMAN; OLIGODENDROGLIA; PRIORITY JOURNAL; RAT; SENSITIVITY AND SPECIFICITY;

ACETYL COENZYME A; CELL DIFFERENTIATION; GENES, MITOCHONDRIAL; HUMANS; METABOLIC NETWORKS AND PATHWAYS; MITOCHONDRIA; OLIGODENDROGLIA; ROTENONE; TRANSCRIPTIONAL ACTIVATION; UNCOUPLING AGENTS;

RODENTIA;

EID: 76049118429     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2009.12.141     Document Type: Article

References (46)

1. Al-Mahdawi S., Pinto R.M., Varshney D., Lawrence L., Lowrie M.B., Hughes S., et al. GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology. Genomics 88 (2006) 580-590
2. Atorino L., Silvestri L., Koppen M., Cassina L., Ballabio A., Marconi R., et al. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J. Cell Biol. 163 (2003) 777-787
3. Baumann N., and Pham-Dinh D. Biology of oligodendrocyte and myelin in the mammalian central nervous system. Physiol. Rev. 81 (2001) 871-927
4. Bizzozero O.A., Sanchez P., and Tetzloff S.U. Effect of ATP depletion on the palmitoylation of myelin proteolipid protein in young and adult rats. J. Neurochem. 72 (1999) 2610-2616
5. Bjorkhem I., and Meaney S. Brain cholesterol: long secret life behind a barrier. Arterioscler. Thromb. Vasc. Biol. 24 (2004) 806-815
6. Buntinx M., Vanderlocht J., Hellings N., Vandenabeele F., Lambrichts I., Raus J., et al. Characterization of three human oligodendroglial cell lines as a model to study oligodendrocyte injury: morphology and oligodendrocyte-specific gene expression. J. Neurocytol. 32 (2003) 25-38
7. Carelli V., Ross-Cisneros F.N., and Sadun A.A. Optic nerve degeneration and mitochondrial dysfunction: genetic and acquired optic neuropathies. Neurochem. Int. 40 (2002) 573-584
8. Cortopassi G., Danielson S., Alemi M., Zhan S.S., Tong W., Carelli V., Martinuzzi A., Marzuki S., Majamaa K., and Wong A. Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts. Mitochondrion 6 (2006) 161-175
9. Deng W., Rosenberg P.A., Volpe J.J., and Jensen F.E. Calcium-permeable AMPA/kainate receptors mediate toxicity and preconditioning by oxygen-glucose deprivation in oligodendrocyte precursors. Proc. Natl. Acad. Sci. USA 100 (2003) 6801-6806
10. Deng W., Yue Q., Rosenberg P.A., Volpe J.J., and Jensen F.E. Oligodendrocyte excitotoxicity determined by local glutamate accumulation and mitochondrial function. J. Neurochem. 98 (2006) 213-222
11. Deng W., Pleasure J., and Pleasure D. Progress in periventricular leukomalacia. Arch. Neurol. 65 (2008) 1291-1295
12. Draghici S., Khatri P., Bhavsar P., Shah A., Krawetz S.A., and Tainsky M.A. Onto-Tools, the toolkit of the modern biologist: Onto-Express, Onto-Compare, Onto-Design and Onto-Translate. Nucleic Acids Res. 31 (2003) 3775-3781
13. Giudetti A.M., Sabetta S., di Summa R., Leo M., Damiano F., Siculella L., et al. Differential effects of coconut oil- and fish oil-enriched diets on tricarboxylate carrier in rat liver mitochondria. J. Lipid Res. 44 (2003) 2135-2141
14. Harding A.E., Sweeney M.G., Miller D.H., Mumford C.J., Kellar-Wood H., Menard D., McDonald W.I., and Compston D.A. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain 115 (1992) 979-989
15. Hirano A., Levine S., and Zimmerman H.M. Experimental cyanide encephalopathy: electron microscopic observations of early lesions in white matter. J. Neuropathol. Exp. Neurol. 26 (1967) 200-213
16. Hirano A., Levine S., and Zimmerman H.M. Remyelination in the central nervous system after cyanide intoxication. J. Neuropathol. Exp. Neurol. 27 (1968) 234-245
17. Hirano A., Zimmerman H.M., and Levine S. Remyelination in the central nervous system after cyanide intoxication. J. Neuropathol. Exp. Neurol. 27 (1968) 144-145
18. Horiuchi M., Itoh A., Pleasure D., and Itoh T. MEK-ERK signaling is involved in interferon-gamma-induced death of oligodendroglial progenitor cells. J. Biol. Chem. 281 (2006) 20095-20106
19. Hu Q.D., Ang B.T., Karsak M., Hu W.P., Cui X.Y., Duka T., et al. F3/contactin acts as a functional ligand for Notch during oligodendrocyte maturation. Cell 115 (2003) 163-175
20. Ishibashi T., Dakin K.A., Stevens B., Lee P.R., Kozlov S.V., Stewart C.L., et al. Astrocytes promote myelination in response to electrical impulses. Neuron 49 (2006) 823-832
21. Itoh T., Beesley J., Itoh A., Cohen A.S., Kavanaugh B., Coulter D.A., et al. AMPA glutamate receptor-mediated calcium signaling is transiently enhanced during development of oligodendrocytes. J. Neurochem. 81 (2002) 390-402
22. Itoh A., Horiuchi M., Bannerman P., Pleasure D., and Itoh T. Impaired regenerative response of primary sensory neurons in ZPK/DLK gene-trap mice. Biochem. Biophys. Res. Commun. 383 (2009) 258-262
23. Johnston P.B., Gaster R.N., Smith V.C., and Tripathi R.C. A clinicopathologic study of autosomal dominant optic atrophy. Am. J. Ophthalmol. 88 (1979) 868-875
24. Kovacs G.G., Hoftberger R., Majtenyi K., Horvath R., Barsi P., Komoly S., et al. Neuropathology of white matter disease in Leber's hereditary optic neuropathy. Brain 128 (2005) 35-41
25. Lessell S., and Kuwabara T. Fine structure of experimental cyanide optic neuropathy. Invest. Ophthalmol. 13 (1974) 748-756
26. Levine S., Hirano A., and Zimmerman H.M. Experimental cyanide encephalopathy: electron microscopic observations of early lesions in white matter. J. Neuropathol. Exp. Neurol. 26 (1967) 172-174
27. Li C., and Hung Wong W. Model-based analysis of oligonucleotide arrays: model validation, design issues and standard error application. Genome Biol. 2 (2001) RESEARCH0032
28. Liu G., Loraine A.E., Shigeta R., Cline M., Cheng J., Valmeekam V., et al. NetAffx: affymetrix probesets and annotations. Nucleic Acids Res. 31 (2003) 82-86
29. Luo Y., and Ingram V.M. Uncoupling of mitochondria activates protein phosphatases and inactivates MBP protein kinases. J. Alzheimers Dis. 3 (2001) 593-598
30. Machkhas H., Bidichandani S.I., Patel P.I., and Harati Y. A mild case of Friedreich ataxia: lymphocyte and sural nerve analysis for GAA repeat length reveals somatic mosaicism. Muscle Nerve 21 (1998) 390-393
31. Morell P., and Jurevics H. Origin of cholesterol in myelin. Neurochem. Res. 21 (1996) 463-470
32. Nielsen J.A., Maric D., Lau P., Barker J.L., and Hudson L.D. Identification of a novel oligodendrocyte cell adhesion protein using gene expression profiling. J. Neurosci. 26 (2006) 9881-9891
33. Niemann A., Berger P., and Suter U. Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease. Neuromolecular Med. 8 (2006) 217-242
34. Ohara S., Ohama E., Takahashi H., Ikuta F., Nishizawa M., Tanaka K., et al. Alterations of oligodendrocytes and demyelination in the spinal cord of patients with mitochondrial encephalomyopathy. J. Neurol. Sci. 86 (1988) 19-29
35. Pleasure D., and Kim S.U. Sterol synthesis by myelinating cultures of mouse spinal cord. Brain Res. 103 (1976) 117-126
36. Rusanen H., Majamaa K., Tolonen U., Remes A.M., Myllyla R., and Hassinen I.E. Demyelinating polyneuropathy in a patient with the tRNA(Leu) (UUR) mutation at base pair 3243 of the mitochondrial DNA. Neurology 45 (1995) 1188-1192
37. Saher G., Brugger B., Lappe-Siefke C., Mobius W., Tozawa R., Wehr M.C., et al. High cholesterol level is essential for myelin membrane growth. Nat. Neurosci. 8 (2005) 468-475
38. Schulz H. Beta oxidation of fatty acids. Biochim. Biophys. Acta 1081 (1991) 109-120
39. Silva J.M., Wong A., Carelli V., and Cortopassi G.A. Inhibition of mitochondrial function induces an integrated stress response in oligodendroglia. Neurobiol. Dis. 34 (2009) 357-365
40. Simons M., and Trajkovic K. Neuron-glia communication in the control of oligodendrocyte function and myelin biogenesis. J. Cell Sci. 119 (2006) 4381-4389
41. Tan G., Chen L.S., Lonnerdal B., Gellera C., Taroni F.A., and Cortopassi G. Frataxin expression rescues mitochondrial dysfunctions in FRDA cells. Hum. Mol. Genet. 10 (2001) 2099-2107
42. Vance J.E., Campenot R.B., and Vance D.E. The synthesis and transport of lipids for axonal growth and nerve regeneration. Biochim. Biophys. Acta 1486 (2000) 84-96
43. Vanopdenbosch L., Dubois B., D'Hooghe M.B., Meire F., and Carton H. Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis. J. Neurol. 247 (2000) 535-543
44. Volpe J.J. Cerebral white matter injury of the premature infant-more common than you think. Pediatrics 112 (2003) 176-180
45. Volpe J.J. Neurology of the Newborn (2008), W.B. Saunders, Philadelphia
46. Wong A., Cavelier L., Collins-Schramm H.E., Seldin M.F., McGrogan M., Savontaus M.L., et al. Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells. Hum. Mol. Genet. 11 (2002) 431-438