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Publication : Time-lapse and cleared imaging of mouse embryonic lung explants to study three-dimensional cell morphology and topology dynamics.

First Author  G?mez HF Year  2023
Journal  STAR Protoc Volume  4
Issue  2 Pages  102187
PubMed ID  36952332 Mgi Jnum  J:380092
Mgi Id  MGI:7640330 Doi  10.1016/j.xpro.2023.102187
Citation  Gomez HF, et al. (2023) Time-lapse and cleared imaging of mouse embryonic lung explants to study three-dimensional cell morphology and topology dynamics. STAR Protoc 4(2):102187
abstractText  Here, we present a protocol for collecting high-spatiotemporal-resolution datasets of undisturbed mouse embryonic epithelial rudiments using light-sheet fluorescence microscopy. We describe steps for rudiment dissection, clearing, and embedding for cleared and live imaging. We then detail procedures for light-sheet imaging followed by image processing and morphometric analysis. We provide protocol variations for imaging both growing and optically cleared lung explants to encourage the quantitative exploration of three-dimensional cell shapes, cell organization, and complex cell-cell dynamics. For complete details on the use and execution of this protocol, please refer to Gomez et al. (2021).(1).
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