Old age potentiates cold-induced tau phosphorylation: linking thermoregulatory deficit with Alzheimer's disease

被引:25
|
作者
Tournissac, Marine [1 ,2 ,3 ]
Vandal, Milene [1 ,2 ,3 ]
Francois, Arnaud [1 ,2 ]
Planel, Emmanuel [2 ,4 ]
Calon, Frederic [1 ,2 ,3 ]
机构
[1] Univ Laval, Fac Pharm, Quebec City, PQ, Canada
[2] CHUL, Ctr Rech, Axe Neurosci, Quebec City, PQ, Canada
[3] Inst Nutr & Aliments Fonct, Quebec City, PQ, Canada
[4] Univ Laval, Fac Med, Dept Psychiat & Neurosci, Quebec City, PQ, Canada
基金
加拿大健康研究院;
关键词
Aging; Thermoregulation; Tau; Alzheimer's disease; Body temperature; BROWN ADIPOSE-TISSUE; COGNITIVE IMPAIRMENT; TEMPERATURE-RANGE; ANIMAL-MODEL; A-BETA; HYPERPHOSPHORYLATION; HYPOTHERMIA; ANESTHESIA; PROTEIN; INHIBITION;
D O I
10.1016/j.neurobiolaging.2016.09.024
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Thermoregulatory deficits coincide with a rise in the incidence of Alzheimer's disease (AD) in old age. Lower body temperature increases tau phosphorylation, a neuropathological hallmark of AD. To determine whether old age potentiates cold-induced tau phosphorylation, we compared the effects of cold exposure (4 degrees C, 24 hours) in 6- and 18-month-old mice. Cold-induced changes in body temperature, brown adipose tissue activity, and phosphorylation of tau at Ser202 were not different between 6- and 18-month-old mice. However, following cold exposure, only old mice displayed a significant rise in soluble tau pThr181 and pThr231, which was correlated with body temperature. Inactivation of glycogen synthase kinase 3 beta was more prominent in young mice, suggesting a protective mechanism against cold-induced tau phosphorylation. These results suggest that old age confers higher susceptibility to tau hyperphosphorylation following a change in body temperature, thereby contributing to an enhanced risk of developing AD. (C) 2016 Elsevier Inc. All rights reserved.
引用
下载
收藏
页码:25 / 29
页数:5
相关论文
共 50 条
  • [1] Repeated cold exposures protect a mouse model of Alzheimer's disease against cold-induced tau phosphorylation
    Tournissac, Marine
    Bourassa, Philippe
    Martinez-Cano, Ruben D.
    Vu, Tra-My
    Hebert, Sebastien S.
    Planel, Emmanuel
    Calon, Frederic
    MOLECULAR METABOLISM, 2019, 22 : 110 - 120
  • [2] Tau phosphorylation in Alzheimer's disease
    Hanger, D
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2003, 13 : S100 - S100
  • [3] Regulation of tau phosphorylation in Alzheimer's disease
    Lee, VMY
    NEUROBIOLOGY OF ALZHEIMER'S DISEASE, 1996, 777 : 107 - 113
  • [4] Epigenetic Modulation on Tau Phosphorylation in Alzheimer's Disease
    Yu, Chao-Chao
    Jiang, Tao
    Yang, Ao-Fei
    Du, Yan-Jun
    Wu, Miao
    Kong, Li-Hong
    NEURAL PLASTICITY, 2019, 2019
  • [5] Tau phosphorylation and aggregation in Alzheimer's disease pathology
    Avila, J
    FEBS LETTERS, 2006, 580 (12) : 2922 - 2927
  • [6] Tau phosphorylation in Alzheimer's disease: pathogen or protector?
    Lee, HG
    Perry, G
    Moreira, PI
    Garrett, MR
    Liu, Q
    Zhu, XW
    Takeda, A
    Nunomura, A
    Smith, MA
    TRENDS IN MOLECULAR MEDICINE, 2005, 11 (04) : 164 - 169
  • [7] Mediators of tau phosphorylation in the pathogenesis of Alzheimer's disease
    Hanger, Diane P.
    Seereeram, Anjan
    Noble, Wendy
    EXPERT REVIEW OF NEUROTHERAPEUTICS, 2009, 9 (11) : 1647 - 1666
  • [8] Phosphorylation of tau by fyn: Implications for Alzheimer's disease
    Lee, G
    Thangavel, R
    Sharma, VM
    Litersky, JM
    Bhaskar, K
    Fang, SM
    Do, LH
    Andreadis, A
    Van Hoesen, G
    Ksiezak-Reding, H
    JOURNAL OF NEUROSCIENCE, 2004, 24 (09): : 2304 - 2312
  • [9] APP and tau phosphorylation in Alzheimer's disease.
    Davies, P
    DeBernardis, J
    Espinoza, M
    Stahl, M
    Vianna, C
    BRAIN PATHOLOGY, 2000, 10 (04) : 493 - 493
  • [10] LINKING Aβ AND TAU IN LATE-ONSET ALZHEIMER'S DISEASE
    Small, S. A.
    GERONTOLOGIST, 2009, 49 : 143 - 143