Axonal Degeneration during Aging and Its Functional Role in Neurodegenerative Disorders

被引:127
|
作者
Salvadores, Natalia [1 ,2 ]
Sanhueza, Mario [1 ,2 ]
Manque, Patricio [1 ]
Court, Felipe A. [1 ,2 ]
机构
[1] Univ Mayor, Ctr Integrat Biol, Fac Sci, Santiago, Chile
[2] Fondap Gerosci Ctr Brain Hlth & Metab, Santiago, Chile
基金
以色列科学基金会; 加拿大健康研究院;
关键词
axonal degeneration; aging; neurodegeneration; disease models; axonopathy; UNFOLDED PROTEIN RESPONSE; AMYOTROPHIC-LATERAL-SCLEROSIS; ENDOPLASMIC-RETICULUM STRESS; DELAYS WALLERIAN DEGENERATION; PERMEABILITY TRANSITION PORE; MITOCHONDRIAL-DNA REPAIR; ALPHA-SYNUCLEIN TOXICITY; TRANSGENIC MOUSE MODELS; LINKED SOD1 MUTANTS; PARKINSONS-DISEASE;
D O I
10.3389/fnins.2017.00451
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Aging constitutes the main risk factor for the development of neurodegenerative diseases. This represents a major health issue worldwide that is only expected to escalate due to the ever-increasing life expectancy of the population. Interestingly, axonal degeneration, which occurs at early stages of neurodegenerative disorders (ND) such as Alzheimer's disease, Amyotrophic lateral sclerosis, and Parkinson's disease, also takes place as a consequence of normal aging. Moreover, the alteration of several cellular processes such as proteostasis, response to cellular stress and mitochondrial homeostasis, which have been described to occur in the aging brain, can also contribute to axonal pathology. Compelling evidence indicate that the degeneration of axons precedes clinical symptoms in NDs and occurs before cell body loss, constituting an early event in the pathological process and providing a potential therapeutic target to treat neurodegeneration before neuronal cell death. Although, normal aging and the development of neurodegeneration are two processes that are closely linked, the molecular basis of the switch that triggers the transition from healthy aging to neurodegeneration remains unrevealed. In this review we discuss the potential role of axonal degeneration in this transition and provide a detailed overview of the literature and current advances in the molecular understanding of the cellular changes that occur during aging that promote axonal degeneration and then discuss this in the context of ND.
引用
收藏
页数:21
相关论文
共 50 条
  • [41] Heat shock proteins in neurodegenerative disorders and aging
    Rehana K. Leak
    Journal of Cell Communication and Signaling, 2014, 8 : 293 - 310
  • [42] Molecular biology of brain aging and neurodegenerative disorders
    Wisniewski, T
    Frangione, B
    ACTA NEUROBIOLOGIAE EXPERIMENTALIS, 1996, 56 (01) : 267 - 279
  • [43] Stress, aging, and neurodegenerative disorders - Molecular mechanisms
    Busciglio, J
    Andersen, JK
    Schipper, HM
    Gilad, GM
    McCarty, R
    Marzatico, F
    Toussaint, O
    STRESS OF LIFE: FROM MOLECULES TO MAN, 1998, 851 : 429 - 443
  • [44] AGING AND AGE-ASSOCIATED NEURODEGENERATIVE DISORDERS
    PRICE, DL
    CURRENT OPINION IN NEUROLOGY, 1995, 8 (04) : 253 - 255
  • [45] Are pathological lesions in neurodegenerative disorders the cause or the effect of the degeneration?
    Armstrong, RA
    Cairns, NJ
    Lantos, PL
    NEUROPATHOLOGY, 2002, 22 (03) : 133 - 146
  • [46] No. 8 neurodegenerative disorders (2), system degeneration
    Wakabayashi, K
    NEUROLOGICAL SURGERY, 2003, 31 (02): : 216 - 222
  • [47] Brain iron accumulation in aging and neurodegenerative disorders
    Hagemeier, Jesper
    Geurts, Jeroen J. G.
    Zivadinov, Robert
    EXPERT REVIEW OF NEUROTHERAPEUTICS, 2012, 12 (12) : 1467 - 1480
  • [48] NAD+ in Brain Aging and Neurodegenerative Disorders
    Lautrup, Sofie
    Sinclair, David A.
    Mattson, Mark P.
    Fang, Evandro F.
    CELL METABOLISM, 2019, 30 (04) : 630 - 655
  • [49] Mechanisms of olfactory dysfunction in aging and neurodegenerative disorders
    Kovács, T
    AGEING RESEARCH REVIEWS, 2004, 3 (02) : 215 - 232
  • [50] Sirtuins and Their Roles in Brain Aging and Neurodegenerative Disorders
    Henryk Jęśko
    Przemysław Wencel
    Robert P. Strosznajder
    Joanna B. Strosznajder
    Neurochemical Research, 2017, 42 : 876 - 890