NeuriteQuant: An open source toolkit for high content screens of neuronal Morphogenesis

被引:37
作者
Dehmelt, Leif [1 ,3 ]
Poplawski, Gunnar [2 ]
Hwang, Eric [4 ]
Halpain, Shelley [2 ]
机构
[1] Max Planck Inst Mol Physiol, D-44227 Dortmund, Germany
[2] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[3] Dortmund Univ Technol, D-44227 Dortmund, Germany
[4] Natl Chiao Tung Univ, Dept Biol Sci & Technol, Hsinchu 30068, Taiwan
基金
美国国家卫生研究院;
关键词
MAMMALIAN-CELLS; STEM-CELLS; PROTEINS; GROWTH; VALIDATION; EXPRESSION; OUTGROWTH; COMPLEX; IMAGES; ARP2/3;
D O I
10.1186/1471-2202-12-100
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: To date, some of the most useful and physiologically relevant neuronal cell culture systems, such as high density co-cultures of astrocytes and primary hippocampal neurons, or differentiated stem cell-derived cultures, are characterized by high cell density and partially overlapping cellular structures. Efficient analytical strategies are required to enable rapid, reliable, quantitative analysis of neuronal morphology in these valuable model systems. Results: Here we present the development and validation of a novel bioinformatics pipeline called NeuriteQuant. This tool enables fully automated morphological analysis of large-scale image data from neuronal cultures or brain sections that display a high degree of complexity and overlap of neuronal outgrowths. It also provides an efficient web-based tool to review and evaluate the analysis process. In addition to its built-in functionality, NeuriteQuant can be readily extended based on the rich toolset offered by ImageJ and its associated community of developers. As proof of concept we performed automated screens for modulators of neuronal development in cultures of primary neurons and neuronally differentiated P19 stem cells, which demonstrated specific dose-dependent effects on neuronal morphology. Conclusions: NeuriteQuant is a freely available open-source tool for the automated analysis and effective review of large-scale high-content screens. It is especially well suited to quantify the effect of experimental manipulations on physiologically relevant neuronal cultures or brain sections that display a high degree of complexity and overlap among neurites or other cellular structures.
引用
收藏
页数:13
相关论文
共 27 条
[1]   Effects of dynactin disruption and dynein depletion on axonal microtubules [J].
Ahmad, FJ ;
He, Y ;
Myers, KA ;
Hasaka, TP ;
Francis, F ;
Black, MM ;
Baas, PW .
TRAFFIC, 2006, 7 (05) :524-537
[2]   Differentiated neurons retain the capacity to generate axons from dendrites [J].
Bradke, F ;
Dotti, CG .
CURRENT BIOLOGY, 2000, 10 (22) :1467-1470
[3]  
Dahl JP, 2003, J NEUROSCI, V23, P3343
[4]   A microtubule-based, dynein-dependent force induces local cell protrusions: Implications for neurite initiation [J].
Dehmelt, Leif ;
Nalbant, Perihan ;
Steffen, Walter ;
Halpain, Shelley .
BRAIN CELL BIOLOGY, 2006, 35 (01) :39-56
[5]  
Farah MH, 2000, DEVELOPMENT, V127, P693
[6]  
Gallo G, 1999, J NEUROSCI, V19, P3860
[7]  
GOSLIN K, 1991, CULTURING NERVE CELL, P207
[8]   Large-scale sources of neural stem cells [J].
Gottlieb, DI .
ANNUAL REVIEW OF NEUROSCIENCE, 2002, 25 :381-407
[9]   A computational framework for studying neuron morphology from in vitro high content neuron-based screening [J].
Huang, Yue ;
Zhou, Xiaobo ;
Miao, Benchun ;
Lipinski, Marta ;
Zhang, Yong ;
Li, Fuhai ;
Degterev, Alexei ;
Yuan, Junying ;
Hu, Guangshu ;
Wong, Stephen T. C. .
JOURNAL OF NEUROSCIENCE METHODS, 2010, 190 (02) :299-309
[10]  
HUBER G, 1984, J NEUROSCI, V4, P151