Your browser doesn't support javascript.
loading
SOX4 Allows Facultative ß-Cell Proliferation Through Repression of Cdkn1a.
Xu, Eric E; Sasaki, Shugo; Speckmann, Thilo; Nian, Cuilan; Lynn, Francis C.
Afiliação
  • Xu EE; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Sasaki S; Cell and Developmental Biology Graduate Program, University of British Columbia, Vancouver, British Columbia, Canada.
  • Speckmann T; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Nian C; Departments of Surgery and Cellular and Physiological Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Lynn FC; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Diabetes ; 66(8): 2213-2219, 2017 08.
Article em En | MEDLINE | ID: mdl-28495880
ABSTRACT
The high-mobility group box transcription factor SOX4 is the most highly expressed SOX family protein in pancreatic islets, and mutations in Sox4 are associated with an increased risk of developing type 2 diabetes. We used an inducible ß-cell knockout mouse model to test the hypothesis that Sox4 is essential for the maintenance of ß-cell number during the development of type 2 diabetes. Knockout of Sox4 at 6 weeks of age resulted in time-dependent worsening of glucose tolerance, impairment of insulin secretion, and diabetes by 30 weeks of age. Immunostaining revealed a decrease in ß-cell mass in knockout mice that was caused by a 39% reduction in ß-cell proliferation. Gene expression studies revealed that induction of the cell cycle inhibitor Cdkn1a was responsible for the decreased proliferation in the knockout animals. Altogether, this study demonstrates that SOX4 is necessary for adult ß-cell replication through direct regulation of the ß-cell cycle.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proliferação de Células / Diabetes Mellitus Tipo 2 / Células Secretoras de Insulina / Inibidor de Quinase Dependente de Ciclina p21 / Fatores de Transcrição SOXC Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proliferação de Células / Diabetes Mellitus Tipo 2 / Células Secretoras de Insulina / Inibidor de Quinase Dependente de Ciclina p21 / Fatores de Transcrição SOXC Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article