河马信号通路
细胞生物学
生物
干细胞
激酶
类有机物
再生(生物学)
体内
肝再生
细胞生长
体外
生物化学
生物技术
作者
Kenji Namoto,Clara Baader,Vanessa Orsini,Alexandro Landshammer,Eva Breuer,Kieu Trinh Dinh,Rosemarie Ungricht,Monika Pikiolek,Stéphane Laurent,Bo Lü,Alexandra Aebi,Katharina Schönberger,Eric Vangrevelinghe,Olivera Evrova,Tianliang Sun,Stefano Annunziato,Julie Lachal,Emily Redmond,Louis Wang,Kristie Wetzel
出处
期刊:Cell Stem Cell
[Elsevier]
日期:2024-04-01
卷期号:31 (4): 554-569.e17
被引量:17
标识
DOI:10.1016/j.stem.2024.03.003
摘要
The YAP/Hippo pathway is an organ growth and size regulation rheostat safeguarding multiple tissue stem cell compartments. LATS kinases phosphorylate and thereby inactivate YAP, thus representing a potential direct drug target for promoting tissue regeneration. Here, we report the identification and characterization of the selective small-molecule LATS kinase inhibitor NIBR-LTSi. NIBR-LTSi activates YAP signaling, shows good oral bioavailability, and expands organoids derived from several mouse and human tissues. In tissue stem cells, NIBR-LTSi promotes proliferation, maintains stemness, and blocks differentiation in vitro and in vivo. NIBR-LTSi accelerates liver regeneration following extended hepatectomy in mice. However, increased proliferation and cell dedifferentiation in multiple organs prevent prolonged systemic LATS inhibition, thus limiting potential therapeutic benefit. Together, we report a selective LATS kinase inhibitor agonizing YAP signaling and promoting tissue regeneration in vitro and in vivo, enabling future research on the regenerative potential of the YAP/Hippo pathway.
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