作者
Kenji Namoto,Christine D. Baader,Vanessa Orsini,Alexandro Landshammer,Eva Breuer,Kiet Truong Dinh,Rosemarie Ungricht,Monika Pikiolek,Stéphane Laurent,Bo Lü,Alexandra Aebi,Katharina Schönberger,Eric Vangrevelinghe,Olivera Evrova,Tianliang Sun,Stefano Annunziato,Julie Lachal,Everett Redmond,Louis Wang,Kristie Wetzel,Paola Capodieci,Jonathan Turner,Gabi Schutzius,Vincent Unterreiner,Markus Trunzer,Nicole Buschmann,Dirk Behnke,Rainer Machauer,Clemens Scheufler,Christian N. Parker,Magali Ferro,Armelle Grevot,Armin Beyerbach,Wei‐Yu Lu,Stuart J. Forbes,Jürgen Wagner,Tewis Bouwmeester,Jun Liu,Bindi Sohal,Sukhdeep K. Sahambi,Linda E. Greenbaum,Felix Lohmann,Philipp S. Hoppe,Feng Cong,Andreas W. Sailer,Heinz Ruffner,Ralf Glatthar,Bostjan Humar,Pierre–Alain Clavien,Michael T. Dill,Elizabeth George,Jürgen Maibaum,Prisca Liberali,Jan S. Tchorz
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.