Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland; University of Basel, Basel, Switzerland.
Cell Stem Cell. 2024 Apr 4;31(4):554-569.e17. doi: 10.1016/j.stem.2024.03.003.
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.
YAP/Hippo 通路是一种器官生长和大小调节变阻器,可保护多种组织干细胞隔室。LATS 激酶磷酸化并使 YAP 失活,因此代表了促进组织再生的潜在直接药物靶标。在这里,我们报告了选择性小分子 LATS 激酶抑制剂 NIBR-LTSi 的鉴定和表征。NIBR-LTSi 激活 YAP 信号通路,具有良好的口服生物利用度,并可扩增来自几种小鼠和人类组织的类器官。在组织干细胞中,NIBR-LTSi 促进增殖、维持干性,并在体外和体内阻止分化。NIBR-LTSi 可加速小鼠肝切除术后的肝再生。然而,多个器官中增殖增加和细胞去分化会阻止系统 LATS 抑制的延长,从而限制了潜在的治疗益处。总之,我们报告了一种选择性的 LATS 激酶抑制剂,可激动 YAP 信号通路并促进体外和体内组织再生,为 YAP/Hippo 通路的再生潜力的未来研究奠定了基础。