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Live imaging and quantitation of nascent transcription using the MS2/MCP system in the embryo.胚胎中使用 MS2/MCP 系统进行新生转录的实时成像和定量。
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4
Retrograde ERK activation waves drive base-to-apex multicellular flow in murine cochlear duct morphogenesis.逆行 ERK 激活波驱动小鼠耳蜗内淋巴管形态发生中的基底到顶的多细胞流。
Elife. 2021 Mar 5;10:e61092. doi: 10.7554/eLife.61092.
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Control of osteoblast regeneration by a train of Erk activity waves.通过一连串 Erk 活性波控制成骨细胞的再生。
Nature. 2021 Feb;590(7844):129-133. doi: 10.1038/s41586-020-03085-8. Epub 2021 Jan 6.
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8
A tensile ring drives tissue flows to shape the gastrulating amniote embryo.张力环驱动组织流动,从而塑造正在进行原肠胚形成的羊膜动物胚胎。
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Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation.光遗传学抑制 Delta 揭示了组织分化过程中 Notch 信号的数字输出。
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Smooth muscle differentiation shapes domain branches during mouse lung development.平滑肌分化在小鼠肺发育过程中塑造了领域分支。
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通过活体成像揭示上皮形态发生机制。

Revealing epithelial morphogenetic mechanisms through live imaging.

机构信息

Department of Chemical & Biological Engineering, Princeton University, Princeton, NJ 08544, United States.

Department of Chemical & Biological Engineering, Princeton University, Princeton, NJ 08544, United States; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, United States.

出版信息

Curr Opin Genet Dev. 2022 Feb;72:61-68. doi: 10.1016/j.gde.2021.10.007. Epub 2021 Dec 1.

DOI:10.1016/j.gde.2021.10.007
PMID:34864332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8860867/
Abstract

Epithelial morphogenesis is guided by mechanical forces and biochemical signals that vary spatiotemporally. As many morphogenetic events are driven by rapid cellular processes, understanding morphogenesis requires monitoring development in real time. Here, we discuss how live-imaging approaches can help identify morphogenetic mechanisms otherwise missed in static snapshots of development. We begin with a summary of live-imaging strategies, including recent advances that push the limits of spatiotemporal resolution and specimen size. We then describe recent efforts that employ live imaging to uncover morphogenetic mechanisms. We conclude by discussing how information collected from live imaging can be enhanced by genetically encoded biosensors and spatiotemporal perturbation techniques to determine the dynamics of patterning of developmental signals and their importance for guiding morphogenesis.

摘要

上皮形态发生由时空变化的机械力和生化信号指导。由于许多形态发生事件是由快速的细胞过程驱动的,因此要理解形态发生,就需要实时监测发育。在这里,我们讨论了活体成像方法如何帮助识别在发育的静态快照中错过的形态发生机制。我们首先总结了活体成像策略,包括最近在时空分辨率和标本大小方面取得的突破。然后,我们描述了最近利用活体成像来揭示形态发生机制的努力。最后,我们讨论了如何通过遗传编码的生物传感器和时空扰动技术来增强从活体成像中收集的信息,以确定发育信号的模式形成动力学及其对指导形态发生的重要性。