SIRT1, miR-132 and miR-212 link human longevity to Alzheimer’s Disease

被引:0
|
作者
A. Hadar
E. Milanesi
M. Walczak
M. Puzianowska-Kuźnicka
J. Kuźnicki
A. Squassina
P. Niola
C. Chillotti
J. Attems
I. Gozes
D. Gurwitz
机构
[1] Sackler Faculty of Medicine,Department of Human Molecular Genetics and Biochemistry
[2] Tel Aviv University,Department of Cellular and Molecular Medicine
[3] Victor Babes National Institute of Pathology,Institute of Genetics and Animal Breeding
[4] Polish Academy of Sciences,Department of Human Epigenetics
[5] Mossakowski Medical Research Centre,Department of Geriatrics and Gerontology
[6] Medical Centre of Postgraduate Education,Department of Biomedical Sciences
[7] The International Institute of Molecular and Cell Biology,Unit of Clinical Pharmacology
[8] University of Cagliari,Institute of Neuroscience and Newcastle University Institute of Ageing
[9] University Hospital of Cagliari,Adams Super Center for Brain Studies, Sagol School of Neuroscience
[10] Newcastle University,undefined
[11] Tel Aviv University,undefined
来源
Scientific Reports | / 8卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Alzheimer’s Disease (AD) is the most common cause of dementia in the elderly. Centenarians – reaching the age of >100 years while maintaining good cognitive skills – seemingly have unique biological features allowing healthy aging and protection from dementia. Here, we studied the expression of SIRT1 along with miR-132 and miR-212, two microRNAs known to regulate SIRT1, in lymphoblastoid cell lines (LCLs) from 45 healthy donors aged 21 to 105 years and 24 AD patients, and in postmortem olfactory bulb and hippocampus tissues from 14 AD patients and 20 age-matched non-demented individuals. We observed 4.0-fold (P = 0.001) lower expression of SIRT1, and correspondingly higher expression of miR-132 (1.7-fold; P = 0.014) and miR-212 (2.1-fold; P = 0.036), in LCLs from AD patients compared with age-matched healthy controls. Additionally, SIRT1 expression was 2.2-fold (P = 0.001) higher in centenarian LCLs compared with LCLs from individuals aged 56–82 years; while centenarian LCLs miR-132 and miR-212 indicated 7.6-fold and 4.1-fold lower expression, respectively. Correlations of SIRT1, miR-132 and miR-212 expression with cognitive scores were observed for AD patient-derived LCLs and postmortem AD olfactory bulb and hippocampus tissues, suggesting that higher SIRT1 expression, possibly mediated by lower miR-132 and miR-212, may protect aged individuals from dementia and is reflected in their peripheral tissues.
引用
收藏
相关论文
共 50 条
  • [1] SIRT1, miR-132 and miR-212 link human longevity to Alzheimer's Disease
    Hadar, A.
    Milanesi, E.
    Walczak, M.
    Puzianowska-Kuznicka, M.
    Kuznicki, J.
    Squassina, A.
    Niola, P.
    Chillotti, C.
    Attems, J.
    Gozes, I.
    Gurwitz, D.
    SCIENTIFIC REPORTS, 2018, 8
  • [2] miR-212 and miR-132 Are Downregulated in Neurally Derived Plasma Exosomes of Alzheimer's Patients
    Cha, Diana J.
    Mengel, David
    Mustapic, Maja
    Liu, Wen
    Selkoe, Dennis J.
    Kapogiannis, Dimitrios
    Galasko, Douglas
    Rissman, Robert A.
    Bennett, David A.
    Walsh, Dominic M.
    FRONTIERS IN NEUROSCIENCE, 2019, 13
  • [3] miR-212 and miR-132 are dispensable for mouse mammary gland development
    Hiroyuki Kayo
    Kotaro Kiga
    Yoko Fukuda-Yuzawa
    Sebastian Hedlund
    Kazuyoshi Murakami
    Inti A De La Rosa-Velazquez
    Tokuhiro Kimura
    Kouji Shimoda
    Masanobu Tanabe
    Taro Fukao
    Nature Genetics, 2014, 46 : 802 - 804
  • [4] miR-212 and miR-132 are dispensable for mouse mammary gland development
    Ahmet Ucar
    Erdem Erikci
    Olga Ucar
    Kamal Chowdhury
    Nature Genetics, 2014, 46 : 804 - 805
  • [5] miR-212 and miR-132 are dispensable for mouse mammary gland development
    Kayo, Hiroyuki
    Kiga, Kotaro
    Fukuda-Yuzawa, Yoko
    Hedlund, Sebastian
    Murakami, Kazuyoshi
    De La Rosa-Velazquez, Inti A.
    Kimura, Tokuhiro
    Shimoda, Kouji
    Tanabe, Masanobu
    Fukao, Taro
    NATURE GENETICS, 2014, 46 (08) : 802 - 804
  • [6] miR-212 and miR-132 are dispensable for mouse mammary gland development reply
    Ucar, Ahmet
    Erikci, Erdem
    Ucar, Olga
    Chowdhury, Kamal
    NATURE GENETICS, 2014, 46 (08) : 804 - 805
  • [7] Potential prognostic value of miR-132 and miR-212 expression in mCRPC patients
    Pontico, Mariano
    Frantellizzi, Viviana
    Cindolo, Luca
    De Vincentis, Giuseppe
    ARCHIVIO ITALIANO DI UROLOGIA E ANDROLOGIA, 2021, 93 (03) : 373 - 374
  • [8] The miRNome of Alzheimer's disease: consistent downregulation of the miR-132/212 cluster
    Pichler, Sabrina
    Gu, Wei
    Hartl, Daniela
    Gasparoni, Gilles
    Leidinger, Petra
    Keller, Andreas
    Meese, Eckart
    Mayhaus, Manuel
    Hampel, Harald
    Riemenschneider, Matthias
    NEUROBIOLOGY OF AGING, 2017, 50 : 167.e1 - 167.e10
  • [9] miR-132 and miR-212 are increased in pancreatic cancer and target the retinoblastoma tumor suppressor
    Park, Jong-Kook
    Henry, Jon C.
    Jiang, Jinmai
    Esau, Christine
    Gusev, Yuriy
    Lerner, Megan R.
    Postier, Russell G.
    Brackett, Daniel J.
    Schmittgen, Thomas D.
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 406 (04) : 518 - 523
  • [10] MiR-132 and MiR-212 as Regulators of WT1 and GATA2 in Acute Myeloid Leukemia
    Luesink, Maaike
    Nigten, Jeannet
    Knops, Ruth H. J. N.
    de Witte, Theo J. M.
    van der Reijden, Bert A.
    Jansen, Joop H.
    BLOOD, 2009, 114 (22) : 526 - 526