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Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation
Gap junctions (GJs), which are proteinaceous channels, couple adjacent cells by permitting direct exchange of intracellular molecules with low molecular weights. GJ intercellular communication (GJIC) plays a critical role in regulating behaviors of human embryonic stem cells (hESCs), affecting their...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589565/ https://www.ncbi.nlm.nih.gov/pubmed/33106521 http://dx.doi.org/10.1038/s41598-020-75347-4 |
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author | Fan, Zhenzhen Xue, Xufeng Fu, Jianping Deng, Cheri X. |
author_facet | Fan, Zhenzhen Xue, Xufeng Fu, Jianping Deng, Cheri X. |
author_sort | Fan, Zhenzhen |
collection | PubMed |
description | Gap junctions (GJs), which are proteinaceous channels, couple adjacent cells by permitting direct exchange of intracellular molecules with low molecular weights. GJ intercellular communication (GJIC) plays a critical role in regulating behaviors of human embryonic stem cells (hESCs), affecting their proliferation and differentiation. Here we report a novel use of sonoporation that enables single cell intracellular dye loading and dynamic visualization/quantification of GJIC in hESC colonies. By applying a short ultrasound pulse to excite single microbubbles tethered to cell membranes, a transient pore on the cell membrane (sonoporation) is generated which allows intracellular loading of dye molecules and influx of Ca(2+) into single hESCs. We employ live imaging for continuous visualization of intercellular dye transfer and Ca(2+) diffusion in hESC colonies. We quantify cell–cell permeability based on dye diffusion using mass transport models. Our results reveal heterogeneous intercellular connectivity and a variety of spatiotemporal characteristics of intercellular Ca(2+) waves in hESC colonies induced by sonoporation of single cells. |
format | Online Article Text |
id | pubmed-7589565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75895652020-10-28 Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation Fan, Zhenzhen Xue, Xufeng Fu, Jianping Deng, Cheri X. Sci Rep Article Gap junctions (GJs), which are proteinaceous channels, couple adjacent cells by permitting direct exchange of intracellular molecules with low molecular weights. GJ intercellular communication (GJIC) plays a critical role in regulating behaviors of human embryonic stem cells (hESCs), affecting their proliferation and differentiation. Here we report a novel use of sonoporation that enables single cell intracellular dye loading and dynamic visualization/quantification of GJIC in hESC colonies. By applying a short ultrasound pulse to excite single microbubbles tethered to cell membranes, a transient pore on the cell membrane (sonoporation) is generated which allows intracellular loading of dye molecules and influx of Ca(2+) into single hESCs. We employ live imaging for continuous visualization of intercellular dye transfer and Ca(2+) diffusion in hESC colonies. We quantify cell–cell permeability based on dye diffusion using mass transport models. Our results reveal heterogeneous intercellular connectivity and a variety of spatiotemporal characteristics of intercellular Ca(2+) waves in hESC colonies induced by sonoporation of single cells. Nature Publishing Group UK 2020-10-26 /pmc/articles/PMC7589565/ /pubmed/33106521 http://dx.doi.org/10.1038/s41598-020-75347-4 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fan, Zhenzhen Xue, Xufeng Fu, Jianping Deng, Cheri X. Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation |
title | Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation |
title_full | Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation |
title_fullStr | Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation |
title_full_unstemmed | Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation |
title_short | Visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation |
title_sort | visualization and quantification of dynamic intercellular coupling in human embryonic stem cells using single cell sonoporation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589565/ https://www.ncbi.nlm.nih.gov/pubmed/33106521 http://dx.doi.org/10.1038/s41598-020-75347-4 |
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