Fast microfluidic temperature control for high resolution live cell imaging

被引:1
作者
Casquillas, Guilhem Velve [1 ,2 ,4 ]
Fu, Chuanhai [2 ]
Le Berre, Mael [1 ]
Cramer, Jeremy [1 ]
Meance, Sebastien [4 ]
Plecis, Adrien [4 ]
Baigl, Damien [3 ]
Greffet, Jean-Jacques [5 ]
Chen, Yong [3 ]
Piel, Matthieu [1 ]
Tran, Phong T. [1 ,2 ]
机构
[1] Inst Curie, CNRS, UMR 144, F-75005 Paris, France
[2] Univ Penn, Philadelphia, PA 19104 USA
[3] Ecole Normale Super, UMR 8640, F-75231 Paris, France
[4] CNRS, Lab Photon & Nanostruct, F-91460 Marcoussis, France
[5] Univ Paris 11, CNRS, Inst Opt, Lab Charles Fabry, F-91127 Palaiseau, France
关键词
FISSION YEAST; FLUORESCENCE MICROSCOPY; DEVICES; PROTEIN; POLY(DIMETHYLSILOXANE); FABRICATION; POLARITY; MUTANTS; SHAPE; CHIP;
D O I
10.1039/c0lc00222d
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
One major advantage of using genetically tractable model organisms such as the fission yeast Schizosaccharomyces pombe is the ability to construct temperature-sensitive mutations in a gene. The resulting gene product or protein behaves as wildtype at permissive temperatures. At non-permissive or restrictive temperatures the protein becomes unstable and some or all of its functions are abrogated. The protein regains its function when returning to a permissive temperature. In principle, temperature-sensitive mutation enables precise temporal control of protein activity when coupled to a fast temperature controller. Current commercial temperature control devices do not have fast switching capability over a wide range of temperatures, making repeated temperature changes impossible or impractical at the cellular timescale of seconds or minutes. Microfabrication using soft-lithography is emerging as a powerful tool for cell biological research. We present here a simple disposable polydimethylsiloxane (PDMS) based microfluidic device capable of reversibly switching between 5 degrees C and 45 degrees C in less than 10 s. This device allows high-resolution live cell imaging with an oil immersion objective lens. We demonstrate the utility of this device for studying microtubule dynamics throughout the cell cycle.
引用
收藏
页码:484 / 489
页数:6
相关论文
共 50 条
[41]   A simple microfluidic device for live-imaging of the vertical section of epithelial cells [J].
Araki, Seigo ;
Nakano, Masayoshi ;
Tsugane, Mamiko ;
Sunaga, Fumiko ;
Hattori, Mitsuru ;
Nakano, Masahiro ;
Nagai, Takeharu ;
Suzuki, Hiroaki .
ANALYST, 2020, 145 (02) :667-674
[42]   Live-cell imaging probes to track chromatin modification dynamics [J].
Sato, Yuko ;
Nakao, Masaru ;
Kimura, Hiroshi .
MICROSCOPY, 2021, 70 (05) :415-422
[43]   Live cell imaging at the Munich ion microbeam SNAKE - a status report [J].
Drexler, Guido A. ;
Siebenwirth, Christian ;
Drexler, Sophie E. ;
Girst, Stefanie ;
Greubel, Christoph ;
Dollinger, Guenther ;
Friedl, Anna A. .
RADIATION ONCOLOGY, 2015, 10
[44]   Self-adhesive microculture system for extended live cell imaging [J].
Skommer, J. ;
McGuinness, D. ;
Wlodkowic, D. .
BIOTECHNIC & HISTOCHEMISTRY, 2011, 86 (03) :174-180
[45]   Microfluidic cell chips for high-throughput drug screening [J].
Chi, Chun-Wei ;
Ahmed, A. H. Rezwanuddin ;
Dereli-Korkut, Zeynep ;
Wang, Sihong .
BIOANALYSIS, 2016, 8 (09) :921-937
[46]   Super-resolution imaging of fast morphological dynamics of neurons in behaving animals [J].
Zhang, Yujie ;
Bai, Lu ;
Wang, Xin ;
Zhao, Yuchen ;
Zhang, Tianlei ;
Ye, Lichen ;
Du, Xufei ;
Zhang, Zhe ;
Du, Jiulin ;
Wang, Kai .
NATURE METHODS, 2025, 22 (01) :177-186
[47]   Advances and challenges in high-throughput microscopy for live-cell subcellular imaging [J].
Oheim, Martin .
EXPERT OPINION ON DRUG DISCOVERY, 2011, 6 (12) :1299-1315
[48]   High spatiotemporal resolution imaging of fast intrinsic optical signals activated by retinal flicker stimulation [J].
Li, Yang-Guo ;
Zhang, Qiu-Xiang ;
Liu, Lei ;
Amthor, Franklin R. ;
Yao, Xin-Cheng .
OPTICS EXPRESS, 2010, 18 (07) :7210-7218
[49]   Extremely high spatiotemporal resolution microscopy for live cell imaging by single photon counting, noise elimination, and a novel restoration algorithm based on probability calculation [J].
Miyashiro, Daisuke ;
Tojima, Takuro ;
Nakano, Akihiko .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2024, 12
[50]   On-chip CO2 control for microfluidic cell culture [J].
Forry, Samuel P. ;
Locascio, Laurie E. .
LAB ON A CHIP, 2011, 11 (23) :4041-4046