Literature DB >> 22760670

A microfluidic device that forms and redirects pheromone gradients to study chemotropism in yeast.

Marie-Elena Brett1, Reagan DeFlorio, David E Stone, David T Eddington.   

Abstract

Chemotropism, or directed cell growth in response to a chemical gradient, is integral to many biological processes. The mating response of the budding yeast, Saccharomyces cerevisiae, is a well studied model chemotropic system. Yeast cells of opposite mating type signal their positions by secreting soluble mating pheromones. The mutual exchange of pheromones induces the cells to grow towards one another, resulting in mating projections or "shmoos." Yeast cells exhibit a remarkable ability to orient their growth toward the nearest potential mating partner, and to reorient (i.e., bend their mating projections) in response to a change in the direction of the pheromone gradient. Although a number of microfluidic devices have been used to generate linear pheromone gradients and to measure initial orientation, none of them have the capability to change the direction of the gradient, other than to invert it. We have developed a microfluidic device that can produce stable pheromone gradients and rapidly rotate them in 90° increments, mimicking the dynamic gradients yeast are exposed to in situ, and allowing for the study of reorientation as well as initial orientation. The mean angle of orientation exhibited by gradient-stimulated yeast cells in this device was 56.9°. In control experiments, cells subjected to pheromone coming from all four directions showed no evidence of orientation. Switching the direction of the pheromone source by 90° induced 83.6% of the polarized cells to change their direction of growth. Of these, 85.2% bent their mating projections toward the second source, demonstrating the utility of this device in the study of reorientation with specifically controlled gradients.

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Year:  2012        PMID: 22760670     DOI: 10.1039/c2lc40398f

Source DB:  PubMed          Journal:  Lab Chip        ISSN: 1473-0189            Impact factor:   6.799


  7 in total

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Authors:  Marie-Elena Brett; Heather E Bomberger; Geneva R Doak; Matthew A Price; James B McCarthy; David K Wood
Journal:  Integr Biol (Camb)       Date:  2018-04-23       Impact factor: 2.192

Review 2.  Micro total analysis systems: fundamental advances and applications in the laboratory, clinic, and field.

Authors:  Michelle L Kovarik; Douglas M Ornoff; Adam T Melvin; Nicholas C Dobes; Yuli Wang; Alexandra J Dickinson; Philip C Gach; Pavak K Shah; Nancy L Allbritton
Journal:  Anal Chem       Date:  2012-12-04       Impact factor: 6.986

3.  Chemotropism among populations of yeast cells with spatiotemporal resolution in a biofabricated microfluidic platform.

Authors:  Thanh Vo; Sameer B Shah; John S Choy; Xiaolong Luo
Journal:  Biomicrofluidics       Date:  2020-01-17       Impact factor: 2.800

4.  Microfluidic Platforms for Yeast-Based Aging Studies.

Authors:  Myeong Chan Jo; Lidong Qin
Journal:  Small       Date:  2016-09-26       Impact factor: 13.281

5.  Simultaneous or Sequential Orthogonal Gradient Formation in a 3D Cell Culture Microfluidic Platform.

Authors:  Sebastien G M Uzel; Ovid C Amadi; Taylor M Pearl; Richard T Lee; Peter T C So; Roger D Kamm
Journal:  Small       Date:  2015-11-30       Impact factor: 13.281

6.  Using microfluidic chip to form brain-derived neurotrophic factor concentration gradient for studying neuron axon guidance.

Authors:  Hui Huang; Lili Jiang; Shu Li; Jun Deng; Yan Li; Jie Yao; Biyuan Li; Junsong Zheng
Journal:  Biomicrofluidics       Date:  2014-02-19       Impact factor: 2.800

7.  Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae.

Authors:  Manuella R Clark-Cotton; Nicholas T Henderson; Michael Pablo; Debraj Ghose; Timothy C Elston; Daniel J Lew
Journal:  Mol Biol Cell       Date:  2021-03-10       Impact factor: 4.138

  7 in total

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