Opportunities and challenges for using the zebrafish to study neuronal connectivity as an endpoint of developmental neurotoxicity

被引:20
作者
Miller, Galen W. [1 ]
Chandrasekaran, Vidya [2 ]
Yaghoobi, Bianca [1 ]
Lein, Pamela J. [1 ]
机构
[1] Univ Calif Davis, Dept Mol Biosci, 1089 Vet Med Dr, Davis, CA 95616 USA
[2] St Marys Coll Calif, Dept Biol, Moraga, CA 94575 USA
基金
美国国家环境保护局;
关键词
Axons; Dendrites; Developmental neurotoxicity (DNT); In vivo imaging; Neuronal connectivity; Screening platform; Synapses; Zebrafish; WHOLE-BRAIN ACTIVITY; CELLULAR RESOLUTION; DENDRITIC GROWTH; AUTISM; GENE; EXPRESSION; DYNAMICS; GAL4; ELECTROPORATION; THROUGHPUT;
D O I
10.1016/j.neuro.2018.04.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chemical exposures have been implicated as environmental risk factors that interact with genetic susceptibilities to influence individual risk for complex neurodevelopmental disorders, including autism spectrum disorder, schizophrenia, attention deficit hyperactivity disorder and intellectual disabilities. Altered patterns of neuronal connectivity represent a convergent mechanism of pathogenesis for these and other neurodevelopmental disorders, and growing evidence suggests that chemicals can interfere with specific signaling pathways that regulate the development of neuronal connections. There is, therefore, a growing interest in developing screening platforms to identify chemicals that alter neuronal connectivity. Cell-cell, cell-matrix interactions and systemic influences are known to be important in defining neuronal connectivity in the developing brain, thus, a systems-based model offers significant advantages over cell-based models for screening chemicals for effects on neuronal connectivity. The embryonic zebrafish represents a vertebrate model amenable to higher throughput chemical screening that has proven useful in characterizing conserved mechanisms of neurodevelopment. Moreover, the zebrafish is readily amenable to gene editing to integrate genetic susceptibilities. Although use of the zebrafish model in toxicity testing has increased in recent years, the diverse tools available for imaging structural differences in the developing zebrafish brain have not been widely applied to studies of the influence of gene by environment interactions on neuronal connectivity in the developing zebrafish brain. Here, we discuss tools available for imaging of neuronal connectivity in the developing zebrafish, review what has been published in this regard, and suggest a path forward for applying this information to developmental neurotoxicity testing. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:102 / 111
页数:10
相关论文
共 117 条
[1]  
Ahrens MB, 2013, NAT METHODS, V10, P413, DOI [10.1038/nmeth.2434, 10.1038/NMETH.2434]
[2]   Brain-wide neuronal dynamics during motor adaptation in zebrafish [J].
Ahrens, Misha B. ;
Li, Jennifer M. ;
Orger, Michael B. ;
Robson, Drew N. ;
Schier, Alexander F. ;
Engert, Florian ;
Portugues, Ruben .
NATURE, 2012, 485 (7399) :471-U80
[3]   Optimization of a GCaMP Calcium Indicator for Neural Activity Imaging [J].
Akerboom, Jasper ;
Chen, Tsai-Wen ;
Wardill, Trevor J. ;
Tian, Lin ;
Marvin, Jonathan S. ;
Mutlu, Sevinc ;
Calderon, Nicole Carreras ;
Esposti, Federico ;
Borghuis, Bart G. ;
Sun, Xiaonan Richard ;
Gordus, Andrew ;
Orger, Michael B. ;
Portugues, Ruben ;
Engert, Florian ;
Macklin, John J. ;
Filosa, Alessandro ;
Aggarwal, Aman ;
Kerr, Rex A. ;
Takagi, Ryousuke ;
Kracun, Sebastian ;
Shigetomi, Eiji ;
Khakh, Baljit S. ;
Baier, Herwig ;
Lagnado, Leon ;
Wang, Samuel S. -H. ;
Bargmann, Cornelia I. ;
Kimmel, Bruce E. ;
Jayaraman, Vivek ;
Svoboda, Karel ;
Kim, Douglas S. ;
Schreiter, Eric R. ;
Looger, Loren L. .
JOURNAL OF NEUROSCIENCE, 2012, 32 (40) :13819-13840
[4]   Imaging of Neural Ensemble for the Retrieval of a Learned Behavioral Program [J].
Aoki, Tazu ;
Kinoshita, Masae ;
Aoki, Ryo ;
Agetsuma, Masakazu ;
Aizawa, Hidenori ;
Yamazaki, Masako ;
Takahoko, Mikako ;
Amo, Ryunosuke ;
Arata, Akiko ;
Higashijima, Shin-ichi ;
Tsuboi, Takashi ;
Okamoto, Hitoshi .
NEURON, 2013, 78 (05) :881-894
[5]  
Asakawa K, 2008, DEV GROWTH DIFFER, V50, P391, DOI [10.1111/j.1440-169x.2008.01044.x, 10.1111/j.1440-169X.2008.01044.x]
[6]   Genetic dissection of neural circuits by Tol2 transposon-mediated Gal4 gene and enhancer trapping in zebrafish [J].
Asakawa, Kazuhide ;
Suster, Maximiliano L. ;
Mizusawa, Kanta ;
Nagayoshi, Saori ;
Kotani, Tomoya ;
Urasaki, Akihiro ;
Kishimoto, Yasuyuki ;
Hibi, Masahiko ;
Kawakami, Koichi .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (04) :1255-1260
[7]   Zebrafish models of human motor neuron diseases: Advantages and limitations [J].
Babin, Patrick J. ;
Goizet, Cyril ;
Raldua, Demetrio .
PROGRESS IN NEUROBIOLOGY, 2014, 118 :36-58
[8]   Advancing the Science of Developmental Neurotoxicity (DNT): Testing for Better Safety Evaluation [J].
Bal-Price, Anna K. ;
Coecke, Sandra ;
Costa, Lucio ;
Crofton, Kevin M. ;
Fritsche, Ellen ;
Goldberg, Alan ;
Grandjean, Philippe ;
Lein, Pamela J. ;
Li, Abby ;
Lucchini, Roberto ;
Mundy, William R. ;
Padilla, Stephanie ;
Persico, Antonio M. ;
Seiler, Andrea E. M. ;
Kreysa, Joachim .
ALTEX-ALTERNATIVES TO ANIMAL EXPERIMENTATION, 2012, 29 (02) :202-215
[9]   In vitro developmental neurotoxicity (DNT) testing: Relevant models and endpoints [J].
Bal-Price, Anna K. ;
Hogberg, Helena T. ;
Buzanska, Leonora ;
Lenas, Petros ;
van Vliet, Erwin ;
Hartung, Thomas .
NEUROTOXICOLOGY, 2010, 31 (05) :545-554
[10]   Evolution of complexity in the zebrafish synapse proteome [J].
Bayes, Alex ;
Collins, Mark O. ;
Reig-Viader, Rita ;
Gou, Gemma ;
Goulding, David ;
Izquierdo, Abril ;
Choudhary, Jyoti S. ;
Emes, Richard D. ;
Grant, Seth G. N. .
NATURE COMMUNICATIONS, 2017, 8