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FGF8-mediated signaling regulates tooth developmental pace during odontogenesis.
Lin, Chensheng; Ruan, Ningsheng; Li, Linjun; Chen, Yibin; Hu, Xiaoxiao; Chen, YiPing; Hu, Xuefeng; Zhang, Yanding.
Afiliación
  • Lin C; Fujian Key Laboratory of Developmental and Neural Biology and Southern Center for Biomedical Research, College of Life Sciences, Fujian Normal University, Fuzhou, Fujian 350117, China.
  • Ruan N; Fujian Key Laboratory of Developmental and Neural Biology and Southern Center for Biomedical Research, College of Life Sciences, Fujian Normal University, Fuzhou, Fujian 350117, China.
  • Li L; Fujian Key Laboratory of Developmental and Neural Biology and Southern Center for Biomedical Research, College of Life Sciences, Fujian Normal University, Fuzhou, Fujian 350117, China.
  • Chen Y; Fujian Key Laboratory of Developmental and Neural Biology and Southern Center for Biomedical Research, College of Life Sciences, Fujian Normal University, Fuzhou, Fujian 350117, China.
  • Hu X; Fujian Key Laboratory of Developmental and Neural Biology and Southern Center for Biomedical Research, College of Life Sciences, Fujian Normal University, Fuzhou, Fujian 350117, China.
  • Chen Y; Department of Cell and Molecular Biology, Tulane University, New Orleans, LA 70118, USA.
  • Hu X; Fujian Key Laboratory of Developmental and Neural Biology and Southern Center for Biomedical Research, College of Life Sciences, Fujian Normal University, Fuzhou, Fujian 350117, China. Electronic address: bioxfh@fjnu.edu.cn.
  • Zhang Y; Fujian Key Laboratory of Developmental and Neural Biology and Southern Center for Biomedical Research, College of Life Sciences, Fujian Normal University, Fuzhou, Fujian 350117, China. Electronic address: ydzhang@fjnu.edu.cn.
J Genet Genomics ; 49(1): 40-53, 2022 01.
Article en En | MEDLINE | ID: mdl-34500094
ABSTRACT
The developing human and mouse teeth constitute an ideal model system to study the regulatory mechanism underlying organ growth control since their teeth share highly conserved and well-characterized developmental processes, and their developmental tempo varies notably. In the current study, we manipulated heterogenous recombination between human and mouse dental tissues and demonstrated that the dental mesenchyme dominates the tooth developmental tempo and FGF8 could be a critical player during this developmental process. Forced activation of FGF8 signaling in the dental mesenchyme of mice promoted cell proliferation, prevented cell apoptosis via p38 and perhaps PI3K-Akt intracellular signaling, and impelled the transition of the cell cycle from G1- to S-phase in the tooth germ, resulting in the slowdown of the tooth developmental pace. Our results provide compelling evidence that extrinsic signals can profoundly affect tooth developmental tempo, and the dental mesenchymal FGF8 could be a pivotal factor in controlling the developmental pace in a non-cell-autonomous manner during mammalian odontogenesis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diente / Fosfatidilinositol 3-Quinasas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Genet Genomics Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diente / Fosfatidilinositol 3-Quinasas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Genet Genomics Año: 2022 Tipo del documento: Article País de afiliación: China
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