<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Yanagisawa N</submitter><pubmed_abstract>In vivo, tip-growing plant cells need to overcome a series of physical barriers; however, researchers lack the methodology to visualize cellular behavior in such restrictive conditions. To address this issue, we have developed growth chambers for tip-growing plant cells that contain a series of narrow, micro-fabricated gaps (~1 µm) in a poly-dimethylsiloxane (PDMS) substrate. This transparent material allows the user to monitor tip elongation processes in individual cells during microgap penetration by time-lapse imaging. Using this experimental platform, we observed morphological changes in pollen tubes as they penetrated the microgap. We captured the dynamic changes in the shape of a fluorescently labeled vegetative nucleus and sperm cells in a pollen tube during this process. Furthermor</pubmed_abstract><journal>Journal of visualized experiments : JoVE</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6101348</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development of Microfluidic Devices to Study the Elongation Capability of Tip-growing Plant Cells in Extremely Small Spaces.</pubmed_title><pmcid>PMC6101348</pmcid><pubmed_authors>Higashiyama T</pubmed_authors><pubmed_authors>Yanagisawa N</pubmed_authors><pubmed_authors>Sato Y</pubmed_authors><pubmed_authors>Sugimoto N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of Microfluidic Devices to Study the Elongation Capability of Tip-growing Plant Cells in Extremely Small Spaces.</name><description>In vivo, tip-growing plant cells need to overcome a series of physical barriers; however, researchers lack the methodology to visualize cellular behavior in such restrictive conditions. To address this issue, we have developed growth chambers for tip-growing plant cells that contain a series of narrow, micro-fabricated gaps (~1 µm) in a poly-dimethylsiloxane (PDMS) substrate. This transparent material allows the user to monitor tip elongation processes in individual cells during microgap penetration by time-lapse imaging. Using this experimental platform, we observed morphological changes in pollen tubes as they penetrated the microgap. We captured the dynamic changes in the shape of a fluorescently labeled vegetative nucleus and sperm cells in a pollen tube during this process. Furthermor</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 May</publication><modification>2026-06-09T03:23:17.457Z</modification><creation>2026-06-09T03:12:11.298Z</creation></dates><accession>S-EPMC6101348</accession><cross_references><pubmed>29889188</pubmed><doi>10.3791/57262</doi></cross_references></HashMap>