梅尔特克
间充质干细胞
牙槽
气体6
癌症研究
细胞生物学
免疫学
化学
受体酪氨酸激酶
医学
信号转导
生物
牙科
作者
Ann M. Decker,Masanori Matsumoto,Joseph T. Decker,A. Roh,Naohiro Inohara,James V. Sugai,Kelly A. Martin,Russell S. Taichman,Darnell Kaigler,Lonnie D. Shea,Gabriel Núñez
标识
DOI:10.1177/00220345231177996
摘要
Regeneration of alveolar bone is an essential step in restoring healthy function following tooth extraction. Growth of new bone in the healing extraction socket can be variable and often unpredictable when systemic comorbidities are present, leading to the need for additional therapeutic targets to accelerate the regenerative process. One such target is the TAM family (Tyro3, Axl, Mertk) of receptor tyrosine kinases. These proteins have been shown to help resolve inflammation and maintain bone homeostasis and thus may have therapeutic benefits in bone regeneration following extraction. Treatment of mice with a pan-TAM inhibitor (RXDX-106) led to accelerated alveolar bone fill following first molar extraction in a mouse model without changing immune infiltrate. Treatment of human alveolar bone mesenchymal stem cells with RXDX-106 upregulated Wnt signaling and primed the cells for osteogenic differentiation. Differentiation of human alveolar bone mesenchymal stem cells with osteogenic media and TAM-targeted inhibitor RXDX-106 (pan-TAM), ASP-2215 (Axl specific), or MRX-2843 (Mertk specific) showed enhanced mineralization with pan-TAM or Mertk-specific inhibitors and no change with Axl-specific inhibitor. First molar extractions in Mertk
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