2016
DOI: 10.1016/j.semcdb.2015.11.001
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Light-sheet imaging of mammalian development

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Cited by 28 publications
(17 citation statements)
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“…As a result, a tight PBX-dependent regulation of individual target genes and gene networks requires the formation of different context-specific combinatorial complexes that guide distinct developmental programs, a process poorly understood. As high-throughput technology (for reviews, see Spitz and Furlong 2012;Villar et al 2014;Denker and de Laat 2016), live imaging (for reviews, see Saiz et al 2015;de Medeiros et al 2016), single-cell transcriptomics (see Sahakyan and Plath 2016;Regev et al 2017), and system-level approaches (Du et al 2014;Regev et al 2017) are brought to bear, PBX-dependent networks and molecular circuitries will be illuminated in specific morphogenetic contexts and in different cell types at different developmental stages. Ultimately, the availability of encyclopedias of regulatory elements Yue et al 2014) in the genome of different species, together with tissue-specific and temporally controllable LOF animal models to guide functional studies in vivo, will enable a deeper understanding of how various organisms use combinations of regulatory factors and pathways to assume all of the beautiful forms that they display.…”
Section: Concluding Remarks and Perspectivesmentioning
confidence: 99%
“…As a result, a tight PBX-dependent regulation of individual target genes and gene networks requires the formation of different context-specific combinatorial complexes that guide distinct developmental programs, a process poorly understood. As high-throughput technology (for reviews, see Spitz and Furlong 2012;Villar et al 2014;Denker and de Laat 2016), live imaging (for reviews, see Saiz et al 2015;de Medeiros et al 2016), single-cell transcriptomics (see Sahakyan and Plath 2016;Regev et al 2017), and system-level approaches (Du et al 2014;Regev et al 2017) are brought to bear, PBX-dependent networks and molecular circuitries will be illuminated in specific morphogenetic contexts and in different cell types at different developmental stages. Ultimately, the availability of encyclopedias of regulatory elements Yue et al 2014) in the genome of different species, together with tissue-specific and temporally controllable LOF animal models to guide functional studies in vivo, will enable a deeper understanding of how various organisms use combinations of regulatory factors and pathways to assume all of the beautiful forms that they display.…”
Section: Concluding Remarks and Perspectivesmentioning
confidence: 99%
“…Lightsheet microscopy combines high-speed acquisition with low phototoxicity and good optical sectioning at subcellular resolution. Tracking evolving biological processes over a long-term timescale (in days) and using high-speed recordings (seconds or minutes) can bridge different spatial and temporal scales (de Medeiros et al, 2016;Höckendorf et al, 2012). Indeed, light-sheet imaging has been applied to the study of calcium dynamics in plants (Costa et al, 2013), clathrin dynamics, organelle reorganization and cell migration in zebrafish (Liu et al, 2018), division dynamics in tumor spheroids (Lorenzo et al, 2011), mouse intestinal organoid development (Serra et al, 2019) and mouse embryo development, both from pre-implantation embryos (Strnad et al, 2016) and from gastrulation to organogenesis with single cell resolution (McDole et al, 2018).…”
Section: Temporally Resolved Single Cell Methodsmentioning
confidence: 99%
“…Due to the excitation with a thin plane of light it has the advantage of fast acquisition and weak perturbation of the sample [4]. The gentle light excitation allows in vivo imaging over long periods of time [5]. Combined with an arrangement providing an extended depth of field, a large volumetric field of view can be explored at high speed [6].…”
Section: Light Sheet Fluorescence Microscopy (Lsfm) Is a Non-destructmentioning
confidence: 99%