Generation of a p16 Reporter Mouse and Its Use to Characterize and Target p16 high Cells In Vivo

• Published in: Cell metabolism 2020-11, Vol.32 (5), p.814
• Main Authors: Omori, Satotaka, Wang, Teh-Wei, Johmura, Yoshikazu, Kanai, Tomomi, Nakano, Yasuhiro, Kido, Taketomo, Susaki, Etsuo A, Nakajima, Takuya, Shichino, Shigeyuki, Ueha, Satoshi, Ozawa, Manabu, Yokote, Kisho, Kumamoto, Soichiro, Nishiyama, Atsuya, Sakamoto, Takeharu, Yamaguchi, Kiyoshi, Hatakeyama, Seira, Shimizu, Eigo, Katayama, Kotoe, Yamada, Yasuhiro, Yamazaki, Satoshi, Iwasaki, Kanako, Miyoshi, Chika, Funato, Hiromasa, Yanagisawa, Masashi, Ueno, Hiroo, Imoto, Seiya, Furukawa, Yoichi, Yoshida, Nobuaki, Matsushima, Kouji, Ueda, Hiroki R, Miyajima, Atsushi, Nakanishi, Makoto
• Format: Article
• Language: English
• ISSN: 1932-7420

Cell senescence plays a key role in age-associated organ dysfunction, but the in vivo pathogenesis is largely unclear. Here, we generated a p16-Cre -tdTomato mouse model to analyze the in vivo characteristics of p16 cells at a single-cell level. We found tdTomato-positive p16 cells detectable in all organs, which were enriched with age. We also found that these cells failed to proliferate and had half-lives ranging from 2.6 to 4.2 months, depending on the tissue examined. Single-cell transcriptomics in the liver and kidneys revealed that p16 cells were present in various cell types, though most dominant in hepatic endothelium and in renal proximal and distal tubule epithelia, and that these cells exhibited heterogeneous senescence-associated phenotypes. Further, elimination of p16 cells ameliorated nonalcoholic steatohepatitis-related hepatic lipidosis and immune cell infiltration. Our new mouse model and single-cell analysis provide a powerful resource to enable the discovery of previously unidentified senescence functions in vivo.