4.8 Article

Long-Term Growth of Moss in Microfluidic Devices Enables Subcellular Studies in Development

Journal

PLANT PHYSIOLOGY
Volume 172, Issue 1, Pages 28-37

Publisher

AMER SOC PLANT BIOLOGISTS
DOI: 10.1104/pp.16.00879

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Funding

  1. National Science Foundation [MCB-1330171]
  2. David and Lucille Packard Foundation
  3. Laura and Arthur Colwin Endowed Summer Research Fellowship Fund from the Marine Biological Laboratory
  4. Burr and Susie Steinbach Fellowship Fund from the Marine Biological Laboratory
  5. Plant Biology Graduate Program at the University of Massachusetts
  6. National Institutes of Health [R15 GM101636]
  7. Laura and Arthur Colwin Endowed Summer Research Fellowship Fund from the Marine Biological Laboratory in Woods Hole, MA
  8. National Institutes of Health-funded Wyoming IDeA Networks of Biomedical Research Excellence program undergraduate research fellowship [P20GM103432]
  9. Direct For Biological Sciences
  10. Div Of Molecular and Cellular Bioscience [1330171] Funding Source: National Science Foundation

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Key developmental processes that occur on the subcellular and cellular level or occur in occluded tissues are difficult to access, let alone image and analyze. Recently, culturing living samples within polydimethylsiloxane (PDMS) microfluidic devices has facilitated the study of hard-to-reach developmental events. Here, we show that an early diverging land plant, Physcomitrella patens, can be continuously cultured within PDMS microfluidic chambers. Because the PDMS chambers are bonded to a coverslip, it is possible to image P. patens development at high resolution over long time periods. Using PDMS chambers, we report that wild-type protonemal tissue grows at the same rate as previously reported for growth on solid medium. Using long-term imaging, we highlight key developmental events, demonstrate compatibility with high-resolution confocal microscopy, and obtain growth rates for a slow-growing mutant. By coupling the powerful genetic tools available to P. patens with long-term growth and imaging provided by PDMS microfluidic chambers, we demonstrate the capability to study cellular and subcellular developmental events in plants directly and in real time.

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