Organotypic brain slice cultures to model neurodegenerative proteinopathies

被引:77
作者
Croft, C. L. [1 ,2 ]
Futch, H. S. [1 ,2 ]
Moore, B. D. [1 ,2 ]
Golde, T. E. [1 ,2 ,3 ]
机构
[1] Univ Florida, Coll Med, Dept Neurosci, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Ctr Translat Res Neurodegenerat Dis, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Med, McKnight Brain Inst, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
Amyloid-beta; Organotypic brain slice cultures; Tau; Neurodegeneration; Proteinopathies; Alzheimer's disease; Microglia; Recombinant adeno-associated virus; FIBRILLARY ACIDIC PROTEIN; TRIPLE-TRANSGENIC MODEL; A-BETA; ALZHEIMERS-DISEASE; HIPPOCAMPAL SLICES; ALPHA-SYNUCLEIN; IN-VITRO; NEUROFIBRILLARY TANGLES; PLAQUE-FORMATION; NEURONAL LOSS;
D O I
10.1186/s13024-019-0346-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Organotypic slice cultures of brain or spinal cord have been a longstanding tool in neuroscience research but their utility for understanding Alzheimer's disease (AD) and other neurodegenerative proteinopathies has only recently begun to be evaluated. Organotypic brain slice cultures (BSCs) represent a physiologically relevant three-dimensional model of the brain. BSCs support all the central nervous system (CNS) cell types and can be produced from brain areas involved in neurodegenerative disease. BSCs can be used to better understand the induction and significance of proteinopathies underlying the development and progression of AD and other neurodegenerative disorders, and in the future may serve as bridging technologies between cell culture and in vivo experiments for the development and evaluation of novel therapeutic targets and strategies. We review the initial development and general use of BSCs in neuroscience research and highlight the advantages of these cultures as an ex vivo model. Subsequently we focus on i) BSC-based modeling of AD and other neurodegenerative proteinopathies ii) use of BSCs to understand mechanisms underlying these diseases and iii) how BSCs can serve as tools to screen for suitable therapeutics prior to in vivo investigations. Finally, we will examine i) open questions regarding the use of such cultures and ii) how emerging technologies such as recombinant adeno-associated viruses (rAAV) may be combined with these models to advance translational research relevant to neurodegenerative disorders.
引用
收藏
页数:11
相关论文
共 107 条
[61]   EFFECT OF BETA-AMYLOID PEPTIDES ON NEURONS IN HIPPOCAMPAL SLICE CULTURES [J].
MALOUF, AT .
NEUROBIOLOGY OF AGING, 1992, 13 (05) :543-551
[62]   Beta-amyloid expression, release and extracellular deposition in aged rat brain slices [J].
Marksteiner, J. ;
Humpel, C. .
MOLECULAR PSYCHIATRY, 2008, 13 (10) :939-952
[63]   Tau protein kinases: Involvement in Alzheimer's disease [J].
Martin, Ludovic ;
Latypova, Xenia ;
Wilson, Cornelia M. ;
Magnaudeix, Amandine ;
Perrin, Marie-Laure ;
Yardin, Catherine ;
Terro, Faraj .
AGEING RESEARCH REVIEWS, 2013, 12 (01) :289-309
[64]   Altered expression of synaptic proteins occurs early during progression of Alzheimer's disease [J].
Masliah, E ;
Mallory, M ;
Alford, M ;
DeTeresa, R ;
Hansen, LA ;
McKeel, DW ;
Morris, JC .
NEUROLOGY, 2001, 56 (01) :127-129
[65]   TREM2 deficiency impairs chemotaxis and microglial responses to neuronal injury [J].
Mazaheri, Fargol ;
Snaidero, Nicolas ;
Kleinberger, Gernot ;
Madore, Charlotte ;
Daria, Anna ;
Werner, Georg ;
Krasemann, Susanne ;
Capell, Anja ;
Truembach, Dietrich ;
Wurst, Wolfgang ;
Brunner, Bettina ;
Bultmann, Sebastian ;
Tahirovic, Sabina ;
Kerschensteiner, Martin ;
Misgeld, Thomas ;
Butovsky, Oleg ;
Haass, Christian .
EMBO REPORTS, 2017, 18 (07) :1186-1198
[66]   Rat brain sagittal organotypic slice cultures as an ex vivo dopamine cell loss system [J].
McCaughey-Chapman, Amy ;
Connor, Bronwen .
JOURNAL OF NEUROSCIENCE METHODS, 2017, 277 :83-87
[67]   Cascade of tau toxicity in inducible hippocampal brain slices and prevention by aggregation inhibitors [J].
Messing, Lars ;
Decker, Jochen Martin ;
Joseph, Maria ;
Mandelkow, Eckhard ;
Mandelkow, Eva-Maria .
NEUROBIOLOGY OF AGING, 2013, 34 (05) :1343-1354
[68]   Cytoskeletal, synaptic, and nuclear protein changes associated with rat interface organotypic hippocampal slice culture development [J].
Mielke, JG ;
Comas, T ;
Woulfe, J ;
Monette, R ;
Chakravarthy, B ;
Mealing, GAR .
DEVELOPMENTAL BRAIN RESEARCH, 2005, 160 (02) :275-286
[69]   The potential for β-structure in the repeat domain of Tau protein determines aggregation, synaptic decay, neuronal loss, and coassembly with endogenous Tau in inducible mouse models of tauopathy [J].
Mocanu, Maria-Magdalena ;
Nissen, Astrid ;
Eckermann, Katrin ;
Khlistunova, Inna ;
Biernat, Jacek ;
Drexler, Dagmar ;
Petrova, Olga ;
Schoenig, Kai ;
Bujard, Hermann ;
Mandelkow, Eckhard ;
Zhou, Lepu ;
Rune, Gabriele ;
Mandelkow, Eva-Maria .
JOURNAL OF NEUROSCIENCE, 2008, 28 (03) :737-748
[70]   β-amyloid peptide toxicity in organotypic hippocampal slice culture involves Akt/PKB, GSK-3β, and PTEN [J].
Nassif, Melissa ;
Hoppe, Juliana ;
Santin, Katiane ;
Frozza, Rudirnar ;
Zamin, Lauren L. ;
Simao, Fabricio ;
Horn, Ana P. ;
Salbego, Christianne .
NEUROCHEMISTRY INTERNATIONAL, 2007, 50 (01) :229-235