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Genetic targeting of the endoderm with claudin-6(CreER)

A full description of the ontogeny of the β cell would guide efforts to generate β cells from embryonic stem cells (ESCs). The first step requires an understanding of definitive endoderm: the genes and signals responsible for its specification, proliferation, and patterning. This report describes a...

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Detalles Bibliográficos
Autores principales: Anderson, William J, Zhou, Qiao, Alcalde, Victor, Kaneko, Osamu F, Blank, Leah J, Sherwood, Richard I, Guseh, J Sawalla, Rajagopal, Jayaraj, Melton, Douglas A
Formato: Texto
Lenguaje:English
Publicado: Wiley-Liss, Inc. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2665265/
https://www.ncbi.nlm.nih.gov/pubmed/18213590
http://dx.doi.org/10.1002/dvdy.21437
Descripción
Sumario:A full description of the ontogeny of the β cell would guide efforts to generate β cells from embryonic stem cells (ESCs). The first step requires an understanding of definitive endoderm: the genes and signals responsible for its specification, proliferation, and patterning. This report describes a global marker of definitive endoderm, Claudin-6 (Cldn6). We report its expression in early development with particular attention to definitive endoderm derivatives. To create a genetic system to drive gene expression throughout the definitive endoderm with both spatial and temporal control, we target the endogenous locus with an inducible Cre recombinase (Cre-ER(T2)) cassette. Cldn6 null mice are viable and fertile with no obvious phenotypic abnormalities. We also report a lineage analysis of the fate of Cldn6-expressing embryonic cells, which is relevant to the development of the pancreas, lung, and liver.