An in vivo screening platform identifies senolytic compounds that target [p16.sup.INK4a+] fibroblasts in lung fibrosis

The appearance of senescent cells in age-related diseases has spurred the search for compounds that can target senescent cells in tissues, termed senolytics. However, a major caveat with current senolytic screens is the use of cell lines as targets where senescence is induced in vitro, which does no...

Full description

Saved in:
Bibliographic Details
Published inThe Journal of clinical investigation Vol. 134; no. 9
Main Authors Lee, Jin Young, Reyes, Nabora S, Ravishankar, Supriya, Zhou, Minqi, Krasilnikov, Maria, Ringler, Christian, Pohan, Grace, Wilson, Chris, Ang, Kenny Kean-Hooi, Wolters, Paul J, Tsukui, Tatsuya, Sheppard, Dean, Arkin, Michelle R, Peng, Tien
Format Journal Article
LanguageEnglish
Published American Society for Clinical Investigation 01.05.2024
Subjects
Aging
Care and treatment
Cells
Diagnosis
Fibrosis
Heat shock proteins
Pulmonary fibrosis
Scientific equipment and supplies industry
United States
California
Online AccessGet full text

Cover

More Information
Summary:The appearance of senescent cells in age-related diseases has spurred the search for compounds that can target senescent cells in tissues, termed senolytics. However, a major caveat with current senolytic screens is the use of cell lines as targets where senescence is induced in vitro, which does not necessarily reflect the identity and function of pathogenic senescent cells in vivo. Here, we developed a new pipeline leveraging a fluorescent murine reporter that allows for isolation and quantification of [p16.sup.Ink4a+] cells in diseased tissues. By high-throughput screening in vitro, precision-cut lung slice (PCLS) screening ex vivo, and phenotypic screening in vivo, we identified a HSP90 inhibitor, XL888, as a potent senolytic in tissue fibrosis. XL888 treatment eliminated pathogenic [p16.sup.Ink4a+] fibroblasts in a murine model of lung fibrosis and reduced fibrotic burden. Finally, XL888 preferentially targeted [p16.sup.INK4a-hi] human lung fibroblasts isolated from patients with idiopathic pulmonary fibrosis (IPF), and reduced [p16.sup.INK4a+] fibroblasts from IPF PCLS ex vivo. This study provides proof of concept for a platform where [p16.sup.INK4a+] cells are directly isolated from diseased tissues to identify compounds with in vivo and ex vivo efficacy in mice and humans, respectively, and provides a senolytic screening platform for other age-related diseases.
ISSN:0021-9738
1558-8238
DOI:10.1172/JCI173371