Mechanochemical actuators of embryonic epithelial contractility
Spatiotemporal regulation of cell contractility coordinates cell shape change to construct tissue architecture and ultimately directs the morphology and function of the organism. Here we show that contractility responses to spatially and temporally controlled chemical stimuli depend much more strong...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2014-10, Vol.111 (40), p.14366-14371 |
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creator | Kim, YongTae Hazar, Melis Vijayraghavan, Deepthi S. Song, Jiho Jackson, Timothy R. Joshi, Sagar D. Messner, William C. Davidson, Lance A. LeDuc, Philip R. |
description | Spatiotemporal regulation of cell contractility coordinates cell shape change to construct tissue architecture and ultimately directs the morphology and function of the organism. Here we show that contractility responses to spatially and temporally controlled chemical stimuli depend much more strongly on intercellular mechanical connections than on biochemical cues in both stimulated tissues and adjacent cells. We investigate how the cell contractility is triggered within an embryonic epithelial sheet by local ligand stimulation and coordinates a long-range contraction response. Our custom micro fluidic control system allows spatiotemporally controlled stimulation with extracellular ATP, which results in locally distinct contractility followed by mechanical strain pattern formation. The stimulationresponse circuit exposed here provides a better understanding of how morphogenetic processes integrate responses to stimulation and how intercellular responses are transmitted across multiple cells. These findings may enable one to create a biological actuator that actively drives morphogenesis. |
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Here we show that contractility responses to spatially and temporally controlled chemical stimuli depend much more strongly on intercellular mechanical connections than on biochemical cues in both stimulated tissues and adjacent cells. We investigate how the cell contractility is triggered within an embryonic epithelial sheet by local ligand stimulation and coordinates a long-range contraction response. Our custom micro fluidic control system allows spatiotemporally controlled stimulation with extracellular ATP, which results in locally distinct contractility followed by mechanical strain pattern formation. The stimulationresponse circuit exposed here provides a better understanding of how morphogenetic processes integrate responses to stimulation and how intercellular responses are transmitted across multiple cells. 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Here we show that contractility responses to spatially and temporally controlled chemical stimuli depend much more strongly on intercellular mechanical connections than on biochemical cues in both stimulated tissues and adjacent cells. We investigate how the cell contractility is triggered within an embryonic epithelial sheet by local ligand stimulation and coordinates a long-range contraction response. Our custom micro fluidic control system allows spatiotemporally controlled stimulation with extracellular ATP, which results in locally distinct contractility followed by mechanical strain pattern formation. The stimulationresponse circuit exposed here provides a better understanding of how morphogenetic processes integrate responses to stimulation and how intercellular responses are transmitted across multiple cells. 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Here we show that contractility responses to spatially and temporally controlled chemical stimuli depend much more strongly on intercellular mechanical connections than on biochemical cues in both stimulated tissues and adjacent cells. We investigate how the cell contractility is triggered within an embryonic epithelial sheet by local ligand stimulation and coordinates a long-range contraction response. Our custom micro fluidic control system allows spatiotemporally controlled stimulation with extracellular ATP, which results in locally distinct contractility followed by mechanical strain pattern formation. The stimulationresponse circuit exposed here provides a better understanding of how morphogenetic processes integrate responses to stimulation and how intercellular responses are transmitted across multiple cells. These findings may enable one to create a biological actuator that actively drives morphogenesis.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>25246549</pmid><doi>10.1073/pnas.1405209111</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate - pharmacology Animals Biochemistry Biological Sciences Cell Shape - drug effects Cells Dextrans - metabolism Embryological stage Embryonic cells Embryos Female Gap Junctions - metabolism Isoquinolines - metabolism Ligands Mechanotransduction, Cellular - drug effects Mechanotransduction, Cellular - physiology Microfluidic Analytical Techniques Microscopy, Confocal Morphogenesis Physical Sciences Rhodamines - metabolism Signal transmission Signals Strain distribution Stromal cells Structural strain Xenopus laevis Zygote - drug effects Zygote - metabolism Zygote - physiology |
title | Mechanochemical actuators of embryonic epithelial contractility |
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