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ETV5 regulates proliferation and cell cycle genes in the INS-1 (832/13) cell line independently of the concentration of secreted insulin.
Díaz-López, Yael E; Pérez-Figueroa, Gloria Erandi; Cázares-Domínguez, Vicenta; Frigolet, María E; Gutiérrez-Aguilar, Ruth.
Afiliação
  • Díaz-López YE; División de Investigación, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), México.
  • Pérez-Figueroa GE; Laboratorio de Investigación en Enfermedades Metabólicas: Obesidad y Diabetes, Hospital Infantil de México "Federico Gómez", México.
  • Cázares-Domínguez V; Unidad de Investigación en Inmunología y Proteómica, Hospital Infantil de México "Federico Gómez", México.
  • Frigolet ME; Laboratorio de Investigación en Enfermedades Metabólicas: Obesidad y Diabetes, Hospital Infantil de México "Federico Gómez", México.
  • Gutiérrez-Aguilar R; Laboratorio de Investigación en Enfermedades Metabólicas: Obesidad y Diabetes, Hospital Infantil de México "Federico Gómez", México.
FEBS Open Bio ; 13(12): 2263-2272, 2023 12.
Article em En | MEDLINE | ID: mdl-37876309
ABSTRACT
The transcription factor E-twenty-six variant 5 (ETV5) regulates acute insulin secretion. Adequate insulin secretion is dependent on pancreatic ß-cell size and cell proliferation, but the effects of ETV5 on proliferation, cell number, and viability, as well as its relationship with insulin secretion, have not been established yet. Here, we partially silenced ETV5 in the INS-1 (832/13) cell line by siRNA transfection and then measured secreted insulin concentration at different time points, observing similar levels to control cells. After 72 h of ETV5 silencing, we observed decreased cell number and proliferation, without any change in viability or apoptosis. Thus, partial silencing of ETV5 modulates cell proliferation in INS-1 (832/13) independently of secreted insulin levels via upregulation of E2F1 and of inhibitors of the cyclin/CDKs complexes (p21Cdkn1a , p27Cdkn1b , and p57Cdkn1c ) and downregulation of cell cycle activators (PAK3 and FOS).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes cdc / Insulina Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes cdc / Insulina Idioma: En Ano de publicação: 2023 Tipo de documento: Article