Cited by 324

The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.

The role of myelin and oligodendrocytes in axonal energy metabolism

Saab, Aiman S, Tzvetanova, Iva D, Nave, Klaus-Armin·2013·Current Opinion in Neurobiology

Abstract

In vertebrates, the myelination of long axons by oligodendrocytes and Schwann cells enables rapid impulse propagation. However, myelin sheaths are not only passive insulators. Oligodendrocytes are also known to support axonal functions and long-term integrity. Some of the underlying mechanisms have now been identified. It could be shown that oligodendrocytes can survive in vivo by aerobic glycolysis. Myelinating oligodendrocytes release lactate through the monocarboxylate transporter MCT1. Lactate is then utilized by axons for mitochondrial ATP generation. Studying axo-glial signalling and energy metabolism will lead to a better understanding of neurodegenerative diseases, in which axonal energy metabolism fails. These include neurological disorders as diverse as multiple sclerosis, leukodystrophies, and amyotrophic lateral sclerosis.

Overview

Integrity signals

Registry

Crossref · 10.1016/j.conb.2013.09.008

Cites

12 of 12 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Research works printed but not linked: 50

  1. Nave, 2008, Axon-glial signaling and the glial support of axon function, Annu Rev Neurosci, 31, 535, 10.1146/annurev.neuro.30.051606.094309 · DOI
  2. Takahashi, 2011, Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia, Prog Neurobiol, 93, 13, 10.1016/j.pneurobio.2010.09.004 · DOI · Paper page
  3. Griffiths, 1998, Axonal swellings and degeneration in mice lacking the major proteolipid of myelin, Science, 280, 1610, 10.1126/science.280.5369.1610 · DOI · Paper page
  4. Tress, 2012, Panglial gap junctional communication is essential for maintenance of myelin in the CNS, J Neurosci, 32, 7499, 10.1523/JNEUROSCI.0392-12.2012 · DOI
  5. Menichella, 2006, Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity, J Neurosci, 26, 10984, 10.1523/JNEUROSCI.0304-06.2006 · DOI
  6. Rash, 2010, Molecular disruptions of the panglial syncytium block potassium siphoning and axonal saltatory conduction: pertinence to neuromyelitis optica and other demyelinating diseases of the central nervous system, Neuroscience, 168, 982, 10.1016/j.neuroscience.2009.10.028 · DOI
  7. Nave, 2010, Myelination and the trophic support of long axons, Nat Rev Neurosci, 11, 275, 10.1038/nrn2797 · DOI · Paper page
  8. David, 1993, Activation of internodal potassium conductance in rat myelinated axons, J Physiol, 472, 177, 10.1113/jphysiol.1993.sp019942 · DOI
  9. Young, 2008, Imaging correlates of decreased axonal Na+/K+ ATPase in chronic multiple sclerosis lesions, Ann Neurol, 63, 428, 10.1002/ana.21381 · DOI
  10. Ohno, 2011, Myelination and axonal electrical activity modulate the distribution and motility of mitochondria at CNS nodes of Ranvier, J Neurosci, 31, 7249, 10.1523/JNEUROSCI.0095-11.2011 · DOI
  11. Zala, 2013, Vesicular glycolysis provides on-board energy for fast axonal transport, Cell, 152, 479, 10.1016/j.cell.2012.12.029 · DOI
  12. Brown, 2001, Metabolic substrates other than glucose support axon function in central white matter, J Neurosci Res, 66, 839, 10.1002/jnr.10081 · DOI · Paper page
  13. Tekkok, 2005, Transfer of glycogen-derived lactate from astrocytes to axons via specific monocarboxylate transporters supports mouse optic nerve activity, J Neurosci Res, 81, 644, 10.1002/jnr.20573 · DOI · Paper page
  14. Wyss, 2011, In vivo evidence for lactate as a neuronal energy source, J Neurosci, 31, 7477, 10.1523/JNEUROSCI.0415-11.2011 · DOI
  15. Wender, 2000, Astrocytic glycogen influences axon function and survival during glucose deprivation in central white matter, J Neurosci, 20, 6804, 10.1523/JNEUROSCI.20-18-06804.2000 · DOI · Paper page
  16. Brown, 2004, Energy transfer from astrocytes to axons: the role of CNS glycogen, Neurochem Int, 45, 529, 10.1016/j.neuint.2003.11.005 · DOI
  17. Magistretti, 2006, Neuron-glia metabolic coupling and plasticity, J Exp Biol, 209, 2304, 10.1242/jeb.02208 · DOI
  18. Kimelberg, 2004, The role of hypotheses in current research, illustrated by hypotheses on the possible role of astrocytes in energy metabolism and cerebral blood flow: from Newton to now, J Cereb Blood Flow Metab, 24, 1235, 10.1097/01.WCB.0000138668.10058.8C · DOI
  19. Dienel, 2013, Astrocytic energetics during excitatory neurotransmission: what are contributions of glutamate oxidation and glycolysis?, Neurochem Int, 63, 244, 10.1016/j.neuint.2013.06.015 · DOI
  20. Almeida, 2001, Different responses of astrocytes and neurons to nitric oxide: the role of glycolytically generated ATP in astrocyte protection, Proc Natl Acad Sci U S A, 98, 15294, 10.1073/pnas.261560998 · DOI · Paper page
  21. Herrero-Mendez, 2009, The bioenergetic and antioxidant status of neurons is controlled by continuous degradation of a key glycolytic enzyme by APC/C-Cdh1, Nat Cell Biol, 11, 747, 10.1038/ncb1881 · DOI · Paper page
  22. Klugmann, 1997, Assembly of CNS myelin in the absence of proteolipid protein, Neuron, 18, 59, 10.1016/S0896-6273(01)80046-5 · DOI
  23. Edgar, 2009, Early ultrastructural defects of axons and axon-glia junctions in mice lacking expression of Cnp1, Glia, 57, 1815, 10.1002/glia.20893 · DOI
  24. Ferguson, 1997, Axonal damage in acute multiple sclerosis lesions, Brain, 120, 393, 10.1093/brain/120.3.393 · DOI · Paper page
  25. Trapp, 2008, Multiple sclerosis: an immune or neurodegenerative disorder?, Annu Rev Neurosci, 31, 247, 10.1146/annurev.neuro.30.051606.094313 · DOI · Paper page
  26. Edgar, 2004, Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia, J Cell Biol, 166, 121, 10.1083/jcb.200312012 · DOI · Paper page
  27. Ferreirinha, 2004, Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport, J Clin Invest, 113, 231, 10.1172/JCI200420138 · DOI · Paper page
  28. Tarrade, 2006, A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition, Hum Mol Genet, 15, 3544, 10.1093/hmg/ddl431 · DOI
  29. Werner, 2007, Proteolipid protein is required for transport of sirtuin 2 into CNS myelin, J Neurosci, 27, 7717, 10.1523/JNEUROSCI.1254-07.2007 · DOI
  30. Rinholm, 2011, Regulation of oligodendrocyte development and myelination by glucose and lactate, J Neurosci, 31, 538, 10.1523/JNEUROSCI.3516-10.2011 · DOI · Paper page
  31. Diaz, 2005, Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency, Hum Mol Genet, 14, 2737, 10.1093/hmg/ddi307 · DOI
  32. Wang, 2011, Acidosis, acid-sensing ion channels, and neuronal cell death, Mol Neurobiol, 44, 350, 10.1007/s12035-011-8204-2 · DOI
  33. Debernardi, 2003, Cell-specific expression pattern of monocarboxylate transporters in astrocytes and neurons observed in different mouse brain cortical cell cultures, J Neurosci Res, 73, 141, 10.1002/jnr.10660 · DOI
  34. Butt, 1994, Morphological changes in oligodendrocytes in the intact mouse optic nerve following intravitreal injection of tumour necrosis factor, J Neuroimmunol, 51, 27, 10.1016/0165-5728(94)90125-2 · DOI
  35. Nikic, 2011, A reversible form of axon damage in experimental autoimmune encephalomyelitis and multiple sclerosis, Nat Med, 17, 495, 10.1038/nm.2324 · DOI · Paper page
  36. Nagan, 2001, Plasmalogens: biosynthesis and functions, Prog Lipid Res, 40, 199, 10.1016/S0163-7827(01)00003-0 · DOI
  37. Braverman, 2012, Functions of plasmalogen lipids in health and disease, Biochim Biophys Acta, 1822, 1442, 10.1016/j.bbadis.2012.05.008 · DOI · Paper page
  38. Edgar, 2010, Demyelination and axonal preservation in a transgenic mouse model of Pelizaeus-Merzbacher disease, EMBO Mol Med, 2, 42, 10.1002/emmm.200900057 · DOI
  39. Ip, 2012, Neuroinflammation by cytotoxic T-lymphocytes impairs retrograde axonal transport in an oligodendrocyte mutant mouse, PLoS One, 7, e42554, 10.1371/journal.pone.0042554 · DOI
  40. Ghosh, 2011, Targeted ablation of oligodendrocytes triggers axonal damage, PLoS One, 6, e22735, 10.1371/journal.pone.0022735 · DOI
  41. Oluich, 2012, Targeted ablation of oligodendrocytes induces axonal pathology independent of overt demyelination, J Neurosci, 32, 8317, 10.1523/JNEUROSCI.1053-12.2012 · DOI
  42. Locatelli, 2012, Primary oligodendrocyte death does not elicit anti-CNS immunity, Nat Neurosci, 15, 543, 10.1038/nn.3062 · DOI
  43. Viader, 2011, Schwann cell mitochondrial metabolism supports long-term axonal survival and peripheral nerve function, J Neurosci, 31, 10128, 10.1523/JNEUROSCI.0884-11.2011 · DOI
  44. Viader, 2013, Aberrant Schwann cell lipid metabolism linked to mitochondrial deficits leads to axon degeneration and neuropathy, Neuron, 77, 886, 10.1016/j.neuron.2013.01.012 · DOI
  45. Nave, 2007, Mechanisms of disease: inherited demyelinating neuropathies—from basic to clinical research, Nat Clin Pract Neurol, 3, 453, 10.1038/ncpneuro0583 · DOI
  46. Zenker, 2013, Novel pathogenic pathways in diabetic neuropathy, Trends Neurosci, 36, 439, 10.1016/j.tins.2013.04.008 · DOI
  47. Kang, 2013, Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis, Nat Neurosci, 16, 571, 10.1038/nn.3357 · DOI · Paper page
  48. Philips, 2013, Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosis, Brain, 136, 471, 10.1093/brain/aws339 · DOI
  49. Bartzokis, 2004, Age-related myelin breakdown: a developmental model of cognitive decline and Alzheimer's disease, Neurobiol Aging, 25, 5, 10.1016/j.neurobiolaging.2003.03.001 · DOI · Paper page
  50. Takahashi, 2013, Roles of glial cells in schizophrenia: possible targets for therapeutic approaches, Neurobiol Dis, 53, 49, 10.1016/j.nbd.2012.11.001 · DOI

Cited by

Sorted by citations

See all 324

Metadata

Authors
Saab, A. S., Tzvetanova, I. D., & Nave, K.-A.
Venue
Current Opinion in Neurobiology
Publisher
Elsevier BV
Published
2013-12
Volume
23
Issue
6
Pages
1065-1072
ISSN
0959-4388
Cited by
324
References
12
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review