Low dose DMSO treatment induces oligomerization and accelerates aggregation of α-synuclein

被引:0
|
作者
Lasse Reimer
Caroline Haikal
Hjalte Gram
Vasileios Theologidis
Gergo Kovacs
Harm Ruesink
Andreas Baun
Janni Nielsen
Daniel Erik Otzen
Jia-Yi Li
Poul Henning Jensen
机构
[1] Aarhus University,Danish Research Institute of Translational Neuroscience
[2] Aarhus University, DANDRITE
[3] Lund University,Department of Biomedicine
[4] Aarhus University,Neural Plasticity and Repair Unit, Wallenberg Neuroscience Center, Department of Experimental Medical Science
[5] China Medical University,Interdisciplinary Nanoscience Center
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Dimethyl sulfoxide (DMSO) is a highly utilized small molecule that serves many purposes in scientific research. DMSO offers unique polar, aprotic and amphiphilic features, which makes it an ideal solvent for a wide variety of both polar and nonpolar molecules. Furthermore, DMSO is often used as a cryoprotectant in cell-based research. However, recent reports suggest that DMSO, even at low concentration, might interfere with important cellular processes, and cause macromolecular changes to proteins where a shift from α-helical to β-sheet structure can be observed. To investigate how DMSO might influence current research, we assessed biochemical and cellular impacts of DMSO treatment on the structure of the aggregation-prone protein α-synuclein, which plays a central role in the etiology of Parkinson’s disease, and other brain-related disorders, collectively termed the synucleinopathies. Here, we found that addition of DMSO increased the particle-size of α-synuclein, and accelerated the formation of seeding-potent fibrils in a dose-dependent manner. These fibrils made in the presence of DMSO were indistinguishable from fibrils made in pure PBS, when assessed by proteolytic digestion, cytotoxic profile and their ability to seed cellular aggregation of α-synuclein. Moreover, as evident through binding to the MJFR-14-6-4-2 antibody, which preferentially recognizes aggregated forms of α-synuclein, and a bimolecular fluorescence complementation assay, cells exposed to DMSO experienced increased aggregation of α-synuclein. However, no observable α-synuclein abnormalities nor differences in neuronal survival were detected after oral DMSO-treatment in either C57BL/6- or α-synuclein transgenic F28 mice. In summary, we demonstrate that low concentrations of DMSO makes α-synuclein susceptible to undergo aggregation both in vitro and in cells. This may affect experimental outcomes when studying α-synuclein in the presence of DMSO, and should call for careful consideration when such experiments are planned.
引用
收藏
相关论文
共 50 条
  • [1] Low dose DMSO treatment induces oligomerization and accelerates aggregation of α-synuclein
    Reimer, Lasse
    Haikal, Caroline
    Gram, Hjalte
    Theologidis, Vasileios
    Kovacs, Gergo
    Ruesink, Harm
    Baun, Andreas
    Nielsen, Janni
    Otzen, Daniel Erik
    Li, Jia-Yi
    Jensen, Poul Henning
    SCIENTIFIC REPORTS, 2022, 12 (01):
  • [2] Polymyxin B accelerates the α-synuclein aggregation
    Mohapatra, Anshuman
    Bohara, Vijay Singh
    Kumar, Sachin
    Chaudhary, Nitin
    BIOPHYSICAL CHEMISTRY, 2021, 277
  • [3] Intranasal administration of trehalose reduces α-synuclein oligomers and accelerates α-synuclein aggregation
    Tanaka, Makoto T.
    Miki, Yasuo
    Mori, Fumiaki
    Kon, Tomoya
    Furukawa, Tomonori
    Shimoyama, Shuji
    Tatara, Yota
    Ozaki, Taku
    Bettencourt, Conceicao
    Warner, Thomas T.
    Wakabayashi, Koichi
    BRAIN COMMUNICATIONS, 2024, 6 (04)
  • [4] Phosphorylation of α-synuclein induces its aggregation
    Mouradian, M
    Junn, E
    Tanaka, M
    Kim, YM
    MOVEMENT DISORDERS, 2004, 19 : S32 - S33
  • [5] LPS INDUCES AGGREGATION OF α-SYNUCLEIN IN MONOCYTES
    Koopman, Herjan
    Jackson, Simon
    Anichtchik, Oleg
    Carroll, Camille
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2015, 86 (11):
  • [6] Alpha-synuclein oligomerization and aggregation: A model will always be a model
    Outeiro, Tiago Fleming
    JOURNAL OF NEUROCHEMISTRY, 2021, 157 (04) : 889 - 890
  • [7] α-Synuclein aggregation at low concentrations
    Afitska, Kseniia
    Fucikova, Anna
    Shvadchak, Volodymyr V.
    Yushchenko, Dmytro A.
    BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2019, 1867 (7-8): : 701 - 709
  • [8] Cholestanol accelerates α-synuclein aggregation and spreading by activating asparagine endopeptidase
    Yu, Ting
    Nie, Shuke
    Bu, Lihong
    Liu, Miao
    He, Juanfeng
    Niu, Xuan
    Feng, Hongyan
    Guo, Jifeng
    Tang, Beisha
    Zhang, Zhaohui
    Ye, Keqiang
    Jiang, Haiqiang
    Chen, Liam
    Zhang, Zhentao
    JCI INSIGHT, 2023, 8 (21)
  • [9] Trehalose-Induced Structural Transition Accelerates Aggregation of α-Synuclein
    Vishal Naik
    Jay Kardani
    Ipsita Roy
    Molecular Biotechnology, 2016, 58 : 251 - 255
  • [10] Trehalose-Induced Structural Transition Accelerates Aggregation of α-Synuclein
    Naik, Vishal
    Kardani, Jay
    Roy, Ipsita
    MOLECULAR BIOTECHNOLOGY, 2016, 58 (04) : 251 - 255