Axon degeneration: Molecular mechanisms of a self-destruction pathway

Axon degeneration is a characteristic event in many neurodegenerative conditions including stroke, glaucoma, and motor neuropathies. However, the molecular pathways that regulate this process remain unclear. Axon loss in chronic neurodegenerative diseases share many morphological features with those in acute injuries, and expression of the Wallerian degeneration slow (WldS) transgene delays nerve degeneration in both events, indicating a common mechanism of axonal self-destruction in traumatic injuries and degenerative diseases. A proposed model of axon degeneration is that nerve insults lead to impaired delivery or expression of a local axonal survival factor, which results in increased intra-axonal calcium levels and calcium-dependent cytoskeletal breakdown.

[1]  D. Holtzman,et al.  Nicotinamide mononucleotide adenylyl transferase 1 protects against acute neurodegeneration in developing CNS by inhibiting excitotoxic-necrotic cell death , 2011, Proceedings of the National Academy of Sciences.

[2]  J. Milbrandt,et al.  Image-based Screening Identifies Novel Roles for IκB Kinase and Glycogen Synthase Kinase 3 in Axonal Degeneration* , 2011, The Journal of Biological Chemistry.

[3]  M. Rolls,et al.  Dendrites Have a Rapid Program of Injury-Induced Degeneration That Is Molecularly Distinct from Developmental Pruning , 2011, The Journal of Neuroscience.

[4]  M. Sereda,et al.  The Wlds transgene reduces axon loss in a Charcot-Marie-Tooth disease 1A rat model and nicotinamide delays post-traumatic axonal degeneration , 2011, Neurobiology of Disease.

[5]  R. Burke,et al.  Akt Suppresses Retrograde Degeneration of Dopaminergic Axons by Inhibition of Macroautophagy , 2011, The Journal of Neuroscience.

[6]  C. Hetz,et al.  Axonal Degeneration Is Mediated by the Mitochondrial Permeability Transition Pore , 2011, The Journal of Neuroscience.

[7]  A. Wright,et al.  Synaptic Protection in the Brain of WldS Mice Occurs Independently of Age but Is Sensitive to Gene-Dose , 2010, PloS one.

[8]  J. Milbrandt,et al.  Axonal Degeneration Is Blocked by Nicotinamide Mononucleotide Adenylyltransferase (Nmnat) Protein Transduction into Transected Axons* , 2010, The Journal of Biological Chemistry.

[9]  J. Milbrandt,et al.  Amyloid Precursor Protein Cleavage-Dependent and -Independent Axonal Degeneration Programs Share a Common Nicotinamide Mononucleotide Adenylyltransferase 1-Sensitive Pathway , 2010, The Journal of Neuroscience.

[10]  R. Ribchester,et al.  Targeting NMNAT1 to Axons and Synapses Transforms Its Neuroprotective Potency In Vivo , 2010, The Journal of Neuroscience.

[11]  V. Mootha,et al.  MICU1 encodes a mitochondrial EF hand protein required for Ca2+ uptake , 2010, Nature.

[12]  M. Freeman,et al.  Wallerian degeneration, wld(s), and nmnat. , 2010, Annual review of neuroscience.

[13]  A. Yaron,et al.  Axonal Degeneration Is Regulated by the Apoptotic Machinery or a NAD+-Sensitive Pathway in Insects and Mammals , 2010, The Journal of Neuroscience.

[14]  P. Stys,et al.  Mechanisms of axonal injury: internodal nanocomplexes and calcium deregulation. , 2010, Trends in molecular medicine.

[15]  Thomas J. Ostendorf,et al.  Mechanisms of acute axonal degeneration in the optic nerve in vivo , 2010, Proceedings of the National Academy of Sciences.

[16]  P. Garnier,et al.  NAD+ Depletion Is Necessary and Sufficient forPoly(ADP-Ribose) Polymerase-1-Mediated Neuronal Death , 2010, The Journal of Neuroscience.

[17]  Q. Zhai,et al.  Nmnat2 delays axon degeneration in superior cervical ganglia dependent on its NAD synthesis activity , 2010, Neurochemistry International.

[18]  J. Gilley,et al.  Endogenous Nmnat2 Is an Essential Survival Factor for Maintenance of Healthy Axons , 2010, PLoS biology.

[19]  G. Gemes,et al.  Axotomy Depletes Intracellular Calcium Stores in Primary Sensory Neurons , 2009, Anesthesiology.

[20]  T. Araki,et al.  Nicotinamide Mononucleotide Adenylyltransferase Expression in Mitochondrial Matrix Delays Wallerian Degeneration , 2009, The Journal of Neuroscience.

[21]  E. B. George,et al.  Axonal degeneration and disorders of the axonal cytoskeleton , 2009 .

[22]  J. Milbrandt,et al.  Nicotinamide Mononucleotide Adenylyl Transferase-Mediated Axonal Protection Requires Enzymatic Activity But Not Increased Levels of Neuronal Nicotinamide Adenine Dinucleotide , 2009, The Journal of Neuroscience.

[23]  A. Bhattacharjee,et al.  NAD+ Activates KNa Channels in Dorsal Root Ganglion Neurons , 2009, The Journal of Neuroscience.

[24]  J. Milbrandt,et al.  A dual leucine kinase–dependent axon self-destruction program promotes Wallerian degeneration , 2009, Nature Neuroscience.

[25]  R. Ribchester,et al.  WldS protein requires Nmnat activity and a short N-terminal sequence to protect axons in mice , 2009, The Journal of cell biology.

[26]  K. Kerr,et al.  WldS requires Nmnat1 enzymatic activity and N16–VCP interactions to suppress Wallerian degeneration , 2009, The Journal of cell biology.

[27]  Marc Tessier-Lavigne,et al.  APP binds DR6 to trigger axon pruning and neuron death via distinct caspases , 2009, Nature.

[28]  C. Holt,et al.  A functional equivalent of endoplasmic reticulum and Golgi in axons for secretion of locally synthesized proteins , 2009, Molecular and Cellular Neuroscience.

[29]  R. Ribchester,et al.  Non-Nuclear WldS Determines Its Neuroprotective Efficacy for Axons and Synapses In Vivo , 2009, The Journal of Neuroscience.

[30]  C. Krarup,et al.  Motor axon excitability during Wallerian degeneration. , 2008, Brain : a journal of neurology.

[31]  J. Milbrandt,et al.  Nmnat Delays Axonal Degeneration Caused by Mitochondrial and Oxidative Stress , 2008, The Journal of Neuroscience.

[32]  P. Hiesinger,et al.  NAD synthase NMNAT acts as a chaperone to protect against neurodegeneration , 2008, Nature.

[33]  Y. Xing,et al.  A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function , 2008, The Journal of Neuroscience.

[34]  Vittorio Porciatti,et al.  Axons of retinal ganglion cells are insulted in the optic nerve early in DBA/2J glaucoma , 2007, The Journal of cell biology.

[35]  Pico Caroni,et al.  Mechanisms of axon degeneration: From development to disease , 2007, Progress in Neurobiology.

[36]  B. Barres,et al.  Why is Wallerian degeneration in the CNS so slow? , 2007, Annual review of neuroscience.

[37]  G. Magni,et al.  Initial-rate kinetics of human NMN-adenylyltransferases: substrate and metal ion specificity, inhibition by products and multisubstrate analogues, and isozyme contributions to NAD+ biosynthesis. , 2007, Biochemistry.

[38]  Q. Zhai,et al.  Identification of a critical site in Wlds: Essential for Nmnat enzyme activity and axon-protective function , 2007, Neuroscience Letters.

[39]  P. Bernardi,et al.  The mitochondrial permeability transition pore and its involvement in cell death and in disease pathogenesis , 2007, Apoptosis.

[40]  Sunil Q. Mehta,et al.  Drosophila NMNAT Maintains Neural Integrity Independent of Its NAD Synthesis Activity , 2006, PLoS biology.

[41]  S. Khoury,et al.  Protecting Axonal Degeneration by Increasing Nicotinamide Adenine Dinucleotide Levels in Experimental Autoimmune Encephalomyelitis Models , 2006, The Journal of Neuroscience.

[42]  Eric D. Hoopfer,et al.  Wlds Protection Distinguishes Axon Degeneration following Injury from Naturally Occurring Developmental Pruning , 2006, Neuron.

[43]  M. Freeman,et al.  The Drosophila Cell Corpse Engulfment Receptor Draper Mediates Glial Clearance of Severed Axons , 2006, Neuron.

[44]  G. Arbuthnott,et al.  Delayed synaptic degeneration in the CNS of Wlds mice after cortical lesion. , 2006, Brain : a journal of neurology.

[45]  Kevin A. Robertson,et al.  The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells. , 2006, Human molecular genetics.

[46]  R. Ribchester,et al.  The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus. , 2005, Molecular biology of the cell.

[47]  M. Coleman Axon degeneration mechanisms: commonality amid diversity , 2005, Nature Reviews Neuroscience.

[48]  M. Ziegler,et al.  Subcellular Compartmentation and Differential Catalytic Properties of the Three Human Nicotinamide Mononucleotide Adenylyltransferase Isoforms* , 2005, Journal of Biological Chemistry.

[49]  P. Stys,et al.  Na+-Dependent Sources of Intra-Axonal Ca2+ Release in Rat Optic Nerve during In Vitro Chemical Ischemia , 2005, The Journal of Neuroscience.

[50]  Hwai-Jong Cheng,et al.  A little nip and tuck: axon refinement during development and axonal injury , 2005, Current Opinion in Neurobiology.

[51]  W. Gu,et al.  A local mechanism mediates NAD-dependent protection of axon degeneration , 2005, The Journal of cell biology.

[52]  L. Luo,et al.  Axon retraction and degeneration in development and disease. , 2005, Annual review of neuroscience.

[53]  Jeff W Lichtman,et al.  In vivo imaging of axonal degeneration and regeneration in the injured spinal cord , 2005, Nature Medicine.

[54]  Jeffrey Robbins,et al.  Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death , 2005, Nature.

[55]  R. Campenot,et al.  Regulation of Wallerian degeneration and nerve growth factor withdrawal-induced pruning of axons of sympathetic neurons by the proteasome and the MEK/Erk pathway , 2005, Molecular and Cellular Neuroscience.

[56]  R. Ribchester,et al.  The progressive nature of Wallerian degeneration in wild-type and slow Wallerian degeneration (WldS) nerves , 2005, BMC Neuroscience.

[57]  R. Ribchester,et al.  A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapses , 2005, The European journal of neuroscience.

[58]  J. Milbrandt,et al.  Increased Nuclear NAD Biosynthesis and SIRT1 Activation Prevent Axonal Degeneration , 2004, Science.

[59]  Changcheng Song,et al.  Molecular perspectives on p97-VCP: progress in understanding its structure and diverse biological functions. , 2004, Journal of structural biology.

[60]  Richard R. Ribchester,et al.  Quantitative and qualitative analysis of Wallerian degeneration using restricted axonal labelling in YFP-H mice , 2004, Journal of Neuroscience Methods.

[61]  David E. Clapham,et al.  The mitochondrial calcium uniporter is a highly selective ion channel , 2004, Nature.

[62]  B. Trapp,et al.  Depolarization-Induced Ca2+ Release in Ischemic Spinal Cord White Matter Involves L-type Ca2+ Channel Activation of Ryanodine Receptors , 2003, Neuron.

[63]  Zhigang He,et al.  Involvement of the Ubiquitin-Proteasome System in the Early Stages of Wallerian Degeneration , 2003, Neuron.

[64]  Caroline Sievers,et al.  Neurites undergoing Wallerian degeneration show an apoptotic-like process with annexin V positive staining and loss of mitochondrial membrane potential , 2003, Neuroscience Research.

[65]  Liqun Luo,et al.  Axon Pruning during Drosophila Metamorphosis Evidence for Local Degeneration and Requirement of the Ubiquitin-Proteasome System , 2003, Neuron.

[66]  J. Sanes,et al.  Inhibiting Axon Degeneration and Synapse Loss Attenuates Apoptosis and Disease Progression in a Mouse Model of Motoneuron Disease , 2003, Current Biology.

[67]  C. Wessig,et al.  The Wlds Mutation Delays Robust Loss of Motor and Sensory Axons in a Genetic Model for Myelin-Related Axonopathy , 2003, The Journal of Neuroscience.

[68]  Daniel Gitler,et al.  Critical calpain‐dependent ultrastructural alterations underlie the transformation of an axonal segment into a growth cone after axotomy of cultured Aplysia neurons , 2003, The Journal of comparative neurology.

[69]  E. Salido,et al.  A missense mutation in Tbce causes progressive motor neuronopathy in mice , 2002, Nature Genetics.

[70]  John T. Finn,et al.  Axonal Self-Destruction and Neurodegeneration , 2002, Science.

[71]  A. Levey,et al.  Very early activation of m-calpain in peripheral nerve during Wallerian degeneration , 2002, Journal of the Neurological Sciences.

[72]  M. Rich,et al.  The WldS protein protects against axonal degeneration: A model of gene therapy for peripheral neuropathy , 2001, Annals of neurology.

[73]  V. Perry,et al.  Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene , 2001, Nature Neuroscience.

[74]  J. Wolf,et al.  Traumatic Axonal Injury Induces Calcium Influx Modulated by Tetrodotoxin-Sensitive Sodium Channels , 2001, The Journal of Neuroscience.

[75]  V. Perry,et al.  A Ufd2/D4Cole1e chimeric protein and overexpression of Rbp7 in the slow Wallerian degeneration (WldS) mouse. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[76]  Yuehua Wu,et al.  Pathogenesis of Axonal Degeneration: Parallels Between Wallerian Degeneration and Vincristine Neuropathy , 2000, Journal of neuropathology and experimental neurology.

[77]  M. Raff,et al.  Evidence That Wallerian Degeneration and Localized Axon Degeneration Induced by Local Neurotrophin Deprivation Do Not Involve Caspases , 2000, The Journal of Neuroscience.

[78]  J. Griffin,et al.  Temperature Modulation Reveals Three Distinct Stages of Wallerian Degeneration , 1999, The Journal of Neuroscience.

[79]  D. Okonkwo,et al.  Postinjury cyclosporin A administration limits axonal damage and disconnection in traumatic brain injury. , 1999, Journal of neurotrauma.

[80]  Lawrence M. Lifshitz,et al.  Close contacts with the endoplasmic reticulum as determinants of mitochondrial Ca2+ responses. , 1998, Science.

[81]  H. M. Fishman,et al.  Endocytotic Formation of Vesicles and Other Membranous Structures Induced by Ca2+ and Axolemmal Injury , 1998, The Journal of Neuroscience.

[82]  G. Clifton,et al.  μ‐Calpain Activation and Calpain‐Mediated Cytoskeletal Proteolysis Following Traumatic Brain Injury , 1996 .

[83]  M. Dubois‐Dauphin,et al.  Bcl-2 overexpression prevents motoneuron cell body loss but not axonal degeneration in a mouse model of a neurodegenerative disease , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[84]  J W Griffin,et al.  Axotomy-induced axonal degeneration is mediated by calcium influx through ion-specific channels , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[85]  J. Griffin,et al.  Delayed Macrophage Responses and Myelin Clearance during Wallerian Degeneration in the Central Nervous System: The Dorsal Radiculotomy Model , 1994, Experimental Neurology.

[86]  T. Deckwerth,et al.  Neurites can remain viable after destruction of the neuronal soma by programmed cell death (apoptosis). , 1994, Developmental biology.

[87]  J. Glass,et al.  Calcium‐Mediated Degeneration of the Axonal Cytoskeleton in the Ola Mouse , 1994, Journal of neurochemistry.

[88]  V. Perry,et al.  Loss of the Compound Action Potential: an Electrophysiological, Biochemical and Morphological Study of Early Events in Axonal Degeneration in the C57BL/Ola Mouse , 1994, The European journal of neuroscience.

[89]  R. S. Smith,et al.  Persistence of Axonal Transport in Isolated Axons of the Mouse , 1993, The European journal of neuroscience.

[90]  M. Spira,et al.  Spatiotemporal Distribution of Ca2+ Following Axotomy and Throughout the Recovery Process of Cultured Aplysia Neurons , 1993, The European journal of neuroscience.

[91]  E. B. George,et al.  Prolonged survival of transected nerve fibres in C57BL/Ola mice is an intrinsic characteristic of the axon , 1993, Journal of neurocytology.

[92]  S. Ludwin,et al.  Delayed wallerian degeneration in the central nervous system of Ola mice: an ultrastructural study , 1992, Journal of the Neurological Sciences.

[93]  R. Jope,et al.  Degradation of Microtubule‐Associated Protein 2 and Brain Spectrin by Calpain: A Comparative Study , 1991, Journal of neurochemistry.

[94]  V. Perry,et al.  Very Slow Retrograde and Wallerian Degeneration in the CNS of C57BL/Ola Mice , 1991, The European journal of neuroscience.

[95]  R. LoPachin,et al.  Effects of Axotomy on Distribution and Concentration of Elements in Rat Sciatic Nerve , 1990, Journal of neurochemistry.

[96]  V. Perry,et al.  Absence of Wallerian Degeneration does not Hinder Regeneration in Peripheral Nerve , 1989, The European journal of neuroscience.

[97]  M. Wallin,et al.  Proteolysis of tubulin and microtubule-associated proteins 1 and 2 by calpain I and II. Difference in sensitivity of assembled and disassembled microtubules. , 1988, Cell calcium.

[98]  Mark Ellisman,et al.  The neuronal endomembrane system. III. The origins of the axoplasmic reticulum and discrete axonal cisternae at the axon hillock , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[99]  L. Lubińska Patterns of Wallerian degeneration of myelinated fibres in short and long peripheral stumps and in isolated segments of rat phrenic nerve. Interpretation of the role of axoplasmic flow of the trophic factor , 1982, Brain Research.

[100]  M H Ellisman,et al.  Microtrabecular structure of the axoplasmic matrix: visualization of cross-linking structures and their distribution , 1980, The Journal of cell biology.

[101]  T. Reese,et al.  Endoplasmic reticulum sequesters calcium in the squid giant axon. , 1978, Science.

[102]  L. Lubińska Early course of wallerian degeneration in myelinated fibres of the rat phrenic nerve , 1977, Brain Research.

[103]  R. Bunge,et al.  EFFECTS OF CALCIUM ION CONCENTRATION ON THE DEGENERATION OF AMPUTATED AXONS IN TISSUE CULTURE , 1973, The Journal of cell biology.

[104]  A. Waller Experiments on the Section of the Glosso-Pharyngeal and Hypoglossal Nerves of the Frog, and Observations of the Alterations Produced Thereby in the Structure of Their Primitive Fibres , 1851, Edinburgh medical and surgical journal.

[105]  Alexei Verkhratsky,et al.  Physiology and pathophysiology of the calcium store in the endoplasmic reticulum of neurons. , 2005, Physiological reviews.

[106]  G. Clifton,et al.  mu-calpain activation and calpain-mediated cytoskeletal proteolysis following traumatic brain injury. , 1996, Journal of Neurochemistry.

[107]  S. Waxman The Axon : structure, function, and pathophysiology , 1995 .

[108]  T. Eagleton,et al.  The Significance Of Theory , 1990 .

[109]  J. Cavanagh The significance of the "dying back" process in experimental and human neurological disease. , 1964, International review of experimental pathology.

[110]  Cavanagh Jb The significance of the "dying back" process in experimental and human neurological disease. , 1964 .

[111]  A. Waller XX. Experiments on the section of the glossopharyngeal and hypoglossal nerves of the frog, and observations of the alterations produced thereby in the structure of their primitive fibres , 1850, Philosophical Transactions of the Royal Society of London.

[112]  D. Spiro,et al.  THE RELATIONSHIP OF BODY SIZE , NERVE CELL SIZE , AXON LENGTH , AND GLIAL DENSITY IN THE CEREBELLUM , 2022 .