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G(0)-G(1) Transition and the Restriction Point in Pancreatic β-Cells In Vivo

Most of our knowledge on cell kinetics stems from in vitro studies of continuously dividing cells. In this study, we determine in vivo cell-cycle parameters of pancreatic β-cells, a largely quiescent population, using drugs that mimic or prevent glucose-induced replication of β-cells in mice. Quiesc...

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Detalles Bibliográficos
Autores principales: Hija, Ayat, Salpeter, Seth, Klochendler, Agnes, Grimsby, Joseph, Brandeis, Michael, Glaser, Benjamin, Dor, Yuval
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900543/
https://www.ncbi.nlm.nih.gov/pubmed/24130333
http://dx.doi.org/10.2337/db12-1035
Descripción
Sumario:Most of our knowledge on cell kinetics stems from in vitro studies of continuously dividing cells. In this study, we determine in vivo cell-cycle parameters of pancreatic β-cells, a largely quiescent population, using drugs that mimic or prevent glucose-induced replication of β-cells in mice. Quiescent β-cells exposed to a mitogenic glucose stimulation require 8 h to enter the G(1) phase of the cell cycle, and this time is prolonged in older age. The duration of G(1), S, and G(2)/M is ∼5, 8, and 6 h, respectively. We further provide the first in vivo demonstration of the restriction point at the G(0)-G(1) transition, discovered by Arthur Pardee 40 years ago. The findings may have pharmacodynamic implications in the design of regenerative therapies aimed at increasing β-cell replication and mass in patients with diabetes.