Method Article

Using Microfluidic Devices to Measure Lifespan and Cellular Phenotypes in Single Budding Yeast Cells

DOI:

10.3791/55412

⸱

March 30th, 2017

In This Article

Summary

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This article presents a protocol optimized for the production of microfluidic chips and the setup of microfluidic experiments to measure the lifespan and cellular phenotypes of single yeast cells.

Abstract

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Budding yeast Saccharomyces cerevisiae is an important model organism in aging research. Genetic studies have revealed many genes with conserved effects on the lifespan across species. However, the molecular causes of aging and death remain elusive. To gain a systematic understanding of the molecular mechanisms underlying yeast aging, we need high-throughput methods to measure lifespan and to quantify various cellular and molecular phenotypes in single cells. Previously, we developed microfluidic devices to track budding yeast mother cells throughout their lifespan while flushing away newborn daughter cells. This article presents a method for preparing microfluidic chips and for setting up microfluidic experiments. Multiple channels can be used to simultaneously track cells under different conditions or from different yeast strains. A typical setup can track hundreds of cells per channel and allow for high-resolution microscope imaging throughout the lifespan of the cells. Our method also allows detailed characterization of the lifespan, molecular markers, cell morphology, and the cell cycle dynamics of single cells. In addition, our microfluidic device is able to trap a significant amount of fresh mother cells that can be identified by downstream image analysis, making it possible to measure the lifespan with higher accuracy.

Introduction

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Budding yeast is a powerful model organism in aging research. However, a conventional lifespan assay in yeast relies on microdissection, which is not only labor intensive but also low throughput1,2. In addition, the traditional microdissection approach does not provide a detailed view of various cellular and molecular features in the single mother cells as they age. The development of microfluidic devices has enabled an automated procedure to measure yeast lifespan as well as to follow molecular markers and various cellular phenotypes throughout the lifespan of the mother cells3,

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Protocol

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1. Silicon Wafer Mold Fabrication

NOTE: The photomask is designed with AutoCAD software and manufactured by a commercial company. This design contains three layers of different patterns (Supplementary File 1). The heights of the first, second, and third layers are about 4 µm, 10 µm, and 50 µm, respectively. The silicon wafer mold was created from the photomask using soft lithography9,10.

  1. Bake a silicon wafer at 200 °C for 10 min to evaporate the water vapor. Spin coat nega....

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Results

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After the experiments, the lifespans of the cells and many cellular and molecular phenotypes can be extracted from the recorded time-lapse images. Since there are a number of different features that can be extracted from each cell, the first step of the analysis is to annotate the cells and events, including the positions and boundaries of the cells and the timing of various events that are being tracked, such as the budding events. These annotations will make it easier to return to the s.......

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Discussion

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The PDMS device needs to be freshly made. Otherwise, the air bubbles caused by inserting tubes into the device will be difficult to remove. Step 3.4 is important to improve the cell loading efficiency by concentrating the cells. To increase the throughput of the experiment, 4 to 6 modules on the same PDMS chip connected to independently operating pumps are typically used to perform 4 to 6 different experiments (different strains or media compositions) simultaneously.

Compared to the convention.......

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Disclosures

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The authors declare that they have no competing financial interests.

Acknowledgements

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This research was supported by NIH Grant AG043080 and the National Natural Science Foundation of China (NSFC), No. 11434001. We thank Lucas Waldburger for proofreading the manuscript.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
3'' <111> silicon waferAddison Engineering
SU-8 2000 and 3000 SeriesMicroChem
Sylgard® 184 Silicone Elastomer Kitellsworth2065622Include Sylgard® silicone elastomer base and curing agent
Petri dishesVWR391-1502
Harris Uni-coreâ„¢ punch (I.D. 0.75 mm)Sigma-Aldrich29002513
24 mm x 40 mm SLIP-RITE® cover glassThermo Fisher Scientific102440
3M Scotch TapeULINES-10223
VWR® Razor BladesVWR55411-050
Pure Ethanol, KoptecVWR64-17-5
Whoosh-Dusterâ„¢VWR16650-027
5 mL BD Syringe (Luer-Lockâ„¢ Tip)Becton, Dickinson and Company309646
PTFE Standard Wall Tubing (100 ft, AWG Size: 22, Nominal ID: 0.028)Component Supply CompanySWTT-22
Needle AssortmentComponent Supply CompanyNEKIT-1
DesiccatorHACH2238300
Lab OvenFisher Scientific13246516GAQ
Nikon TE2000 microscope with 40X and 60X objectiveNikon
Zeiss Axio Observer Z1 with 40X and 60X objectiveZeiss
Syringe PumpLongerpumpTS-1B

References

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  1. Mortimer, R. K., Johnston, J. R. Life span of individual yeast cells. Nature. 183 (4677), 1751-1752 (1959).
  2. Polymenis, M., Kennedy, B. K. Cell biology: High-tech yeast ageing. Nature. 486 (7401), 37-38 (2012).
  3. Xie, Z., et al.

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Tags

Microfluidic DeviceYeast LifespanBudding YeastCell LoadingMicroscope ImagingPDMS ChipFlow RateYeast SampleImage AnalysisCellular Phenotypes

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