Мобильная версия

Доступно журналов:

3 288

Доступно статей:

3 891 637

 

Скрыть метаданые

Автор Nam, Seong-Won
Автор Noort, Danny Van
Автор Yang, Yoonsun
Автор Park, Sungsu
Дата выпуска 2007
dc.description In this study, we introduce a microfluidic device equipped with pneumatically actuated valves, generating a linear gradient of chemoeffectors to quantify the chemotactic response of Tetrahymena pyriformis, a freshwater ciliate. The microfluidic device was fabricated from an elastomer, poly(dimethylsiloxane) (PDMS), using multi-layer soft lithography. The components of the device include electronically controlled pneumatic microvalves, microchannels and microchambers. The linear gradient of the chemoeffectors was established by releasing a chemical from a ciliate-free microchamber into a microchamber containing the ciliate. The ciliate showed chemotactic behaviours by either swimming toward or avoiding the gradient. By counting the number of ciliates residing in each microchamber, we obtained a precise timeâ response curve. The ciliates in the microfluidic device were sensitive enough to be attracted to 10 pmol glycine-proline, which indicates a 10<sup>5</sup> increase in the ciliate's known sensitivity. With the use of blockers, such as dl-2-amino-5-phosphonopentanoic acid (APPA) or lanthanum chloride (LaCl3), we have demonstrated that the NMDA (N-methyl-d-aspartate) receptor plays a critical role in the perception of chemoeffectors, whereas the Ca<sup>2+</sup> channel is related to the motility of the ciliate. These results demonstrate that our microfluidic chemotaxis assay system is useful not only for the study of ciliate chemotaxis but also for a better understanding of the signal transduction mechanism on their receptors.
Формат application.pdf
Издатель Royal Society of Chemistry
Название A biological sensor platform using a pneumatic-valve controlled microfluidic device containing Tetrahymena pyriformis
Тип research-article
DOI 10.1039/b617357h
Electronic ISSN 1473-0189
Print ISSN 1473-0197
Журнал Lab on a Chip
Том 7
Первая страница 638
Последняя страница 640
Аффилиация NamThe authors contributed equally to this work. Seong-Won; 456 Science Building #B, Division of Nano Sciences (BK21 program), Ewha Womans University, Daehyundong
Аффилиация Noort Danny Van; 456 Science Building #B, Division of Nano Sciences (BK21 program), Ewha Womans University, Daehyundong
Аффилиация Yang Yoonsun; 456 Science Building #B, Division of Nano Sciences (BK21 program), Ewha Womans University, Daehyundong
Аффилиация Park Sungsu; 456 Science Building #B, Division of Nano Sciences (BK21 program), Ewha Womans University, Daehyundong
Выпуск 5
Библиографическая ссылка Sauvant, Chemosphere, 1999, 38, 1631
Библиографическая ссылка Leick, J. Microbiol. Methods, 2004, 59, 233
Библиографическая ссылка Kohidai, Biosci. Rep., 1996, 16, 467
Библиографическая ссылка Kohidai, Cell Biol. Int., 1997, 21, 341
Библиографическая ссылка Koyama, Anal. Chem., 2006, 78, 3354
Библиографическая ссылка Jeon, Nat. Biotechnol., 2002, 20, 826
Библиографическая ссылка Mao, Proc. Natl. Acad. Sci. U. S. A., 2003, 100, 5449
Библиографическая ссылка Frevert, Lab Chip, 2006, 6, 849
Библиографическая ссылка Unger, Science, 2000, 288, 113
Библиографическая ссылка Jun, Tetrahedron Lett., 2006, 47, 1051
Библиографическая ссылка Stover, Nucleic Acids Res., 2006, 34, D500
Библиографическая ссылка Nilsson, Eur. J. Protistol., 2003, 39, 468

Скрыть метаданые