Single-Cell Live Imaging.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2019
Historique:
entrez: 28 4 2019
pubmed: 28 4 2019
medline: 31 8 2019
Statut: ppublish

Résumé

Recent fluorescence microscopy allows for high-throughput acquisition of 5D (X, Y, Z, T, and Color) images in various targets such as cultured cells, 3D spheroid/organoid, and even living tissue with single-cell resolution. The technology is considered promising to augment insights on heterogeneous features of both physiological and pathological cell phenotypes, for instance, distinct responses of cancer cells to anticancer drug treatment. Here we overview microscopic applications to capture live cell events for different types of targets, together with a couple of proof of concepts. The 2D live imaging will be exemplified by a FRET-based time-lapse cultured cell imaging, and 3D tissue imaging protocol will be complemented with a method for mouse skin live imaging.

Identifiants

pubmed: 31028651
doi: 10.1007/978-1-4939-9240-9_24
doi:

Substances chimiques

Fluorescent Dyes 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

409-421

Auteurs

Toru Hiratsuka (T)

Centre for Stem Cells and Regenerative Medicine, King's College London, Guy's Hospital, London, UK. toru.hiratsuka@kcl.ac.uk.

Naoki Komatsu (N)

Laboratory for Cell Function Dynamics, RIKEN Center for Brain Science, Wako, Saitama, Japan.

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Classifications MeSH