A multi-trap microfluidic chip enabling longitudinal studies of nerve regeneration in Caenorhabditis elegans

被引:28
作者
Gokce, Sertan Kutal [1 ]
Hegarty, Evan Marley [2 ]
Mondal, Sudip [2 ]
Zhao, Peisen [1 ]
Ghorashian, Navid [3 ]
Hilliard, Massimo A. [4 ]
Ben-Yakar, Adela [1 ,2 ,3 ,5 ]
机构
[1] Univ Texas Austin, Elect & Comp Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Mech Engn, Austin, TX 78712 USA
[3] Univ Texas Austin, Biomed Engn, Austin, TX 78712 USA
[4] Univ Queensland, Queensland Brain Inst, Brisbane, Qld 4072, Australia
[5] Univ Texas Austin, Inst Neurosci, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
C; ELEGANS; AXONAL REGENERATION; MIGRATION; REQUIRES; RNAI; CELL; NEUROSURGERY; OUTGROWTH; PATHWAYS; FUSION;
D O I
10.1038/s41598-017-10302-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several sophisticated microfluidic devices have recently been proposed for femtosecond laser axotomy in the nematode C. elegans for immobilization of the animals for surgery to overcome time-consuming and labor-intensive manual processes. However, nerve regeneration studies require long-term recovery of the animals and multiple imaging sessions to observe the regeneration capabilities of their axons post-injury. Here we present a simple, multi-trap device, consisting of a single PDMS (polydimethylsiloxane) layer, which can immobilize up to 20 animals at the favorable orientation for optical access needed for precise laser surgery and high-resolution imaging. The new device, named "worm hospital" allows us to perform the entire nerve regeneration studies, including on-chip axotomy, post-surgery housing for recovery, and post-recovery imaging all on one microfluidic chip. Utilizing the worm hospital and analysis of mutants, we observed that most but not all neurodevelopmental genes in the Wnt/Frizzled pathway are important for regeneration of the two touch receptor neurons ALM and PLM. Using our new chip, we observed that the cwn-2 and cfz-2 mutations significantly reduced the reconnection possibilities of both neurons without any significant reduction in the regrowth lengths of the severed axons. We observed a similar regeneration phenotype with cwn-1 mutation in ALM neurons only.
引用
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页数:12
相关论文
共 53 条
[1]   Single-synapse ablation and long-term imaging in live C. elegans [J].
Allen, Peter B. ;
Sgro, Allyson E. ;
Chao, Daniel L. ;
Doepker, Byron E. ;
Edgar, J. Scott ;
Shen, Kang ;
Chiu, Daniel T. .
JOURNAL OF NEUROSCIENCE METHODS, 2008, 173 (01) :20-26
[2]   Microfluidic laboratories for C. elegans enhance fundamental studies in biology [J].
Bakhtina, Natalia A. ;
Korvink, Jan G. .
RSC ADVANCES, 2014, 4 (09) :4691-4709
[3]   Microfluidics for the analysis of behavior, nerve regeneration, and neural cell biology in C. elegans [J].
Ben-Yakar, Adela ;
Chronis, Nikos ;
Lu, Hang .
CURRENT OPINION IN NEUROBIOLOGY, 2009, 19 (05) :561-567
[4]  
BRENNER S, 1974, GENETICS, V77, P71
[5]   In vivo Laser Axotomy in C. elegans [J].
Byrne, Alexandra B. ;
Edwards, Tyson J. ;
Hammarlund, Marc .
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2011, (51)
[6]   Laterally Orienting C. elegans Using Geometry at Microscale for High-Throughput Visual Screens in Neurodegeneration and Neuronal Development Studies [J].
Caceres, Ivan de Carlos ;
Valmas, Nicholas ;
Hilliard, Massimo A. ;
Lu, Hang .
PLOS ONE, 2012, 7 (04)
[7]  
Ch'ng' Q, 2003, GENETICS, V164, P1355
[8]   Axon Regeneration Pathways Identified by Systematic Genetic Screening in C. elegans [J].
Chen, Lizhen ;
Wang, Zhiping ;
Ghosh-Roy, Anindya ;
Hubert, Thomas ;
Yan, Dong ;
O'Rourke, Sean ;
Bowerman, Bruce ;
Wu, Zilu ;
Jin, Yishi ;
Chisholm, Andrew D. .
NEURON, 2011, 71 (06) :1043-1057
[9]   Microfluidics for in vivo imaging of neuronal and behavioral activity in Caenorhabditis elegans [J].
Chronis, Nikos ;
Zimmer, Manuel ;
Bargmann, Cornelia I. .
NATURE METHODS, 2007, 4 (09) :727-731
[10]   Automated on-chip rapid microscopy, phenotyping and sorting of C. elegans [J].
Chung, Kwanghun ;
Crane, Matthew M. ;
Lu, Hang .
NATURE METHODS, 2008, 5 (07) :637-643