β‐Galactosidase‐Triggered Photodynamic Elimination of Senescent Cells with a Boron Dipyrromethene‐Based Photosensitizer

Author:

Chu Jacky C. H.1ORCID,Escriche‐Navarro Blanca2345,Xiong Junlong16,García‐Fernández Alba245ORCID,Martínez‐Máñez Ramón2345ORCID,Ng Dennis K. P.1ORCID

Affiliation:

1. Department of Chemistry The Chinese University of Hong Kong Shatin, N.T. Hong Kong China

2. Instituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico Universitat Politècnica de València Universitat de València Valencia 46022 Spain

3. Unidad Mixta de Investigación en Nanomedicina y Sensores Universitat Politècnica e València, Instituto de Investigación Sanitaria La Fe (IIS La Fe) Valencia 46026 Spain

4. Unidad Mixta UPV‐CIPF de Investigación en Mecanismos de Enfermedades y Nanomedicina Universitat Politècnica de València, Centro de Investigación Príncipe Felipe Valencia 46012 Spain

5. CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER‐BBN) Instituto de Salud Carlos III Madrid 28029 Spain

6. Department of Pharmacy The Affiliated Luohu Hospital of Shenzhen University Shenzhen University Shenzhen 518001 China

Abstract

AbstractSenescence is a cellular response having physiological and reparative functions to preserve tissue homeostasis and suppress tumor growth. However, the accumulation of senescent cells would cause deleterious effects that lead to age‐related dysfunctions and cancer progression. Hence, selective detection and elimination of senescent cells are crucial yet remain a challenge. A β‐galactosidase (β‐gal)‐activated boron dipyrromethene (BODIPY)‐based photosensitizer (compound 1) is reported here that can selectively detect and eradicate senescent cells. It contains a galactose moiety connected to a pyridinium BODIPY via a self‐immolative nitrophenylene linker, of which the photoactivity is effectively quenched. Upon interactions with the senescence‐associated β‐gal, it undergoes enzymatic hydrolysis followed by self‐immolation, leading to the release of an activated BODIPY moiety by which the fluorescence emission and singlet oxygen generation are restored. The ability of 1 to detect and eliminate senescent cells is demonstrated in vitro and in vivo, using SK‐Mel‐103 tumor‐bearing mice treated with senescence‐inducing therapy. The results demonstrate that 1 can be selectively activated in senescent cells to trigger a robust senolytic effect upon irradiation. This study breaks new ground in the design and application of new senolytic agents based on photodynamic therapy.

Funder

Generalitat Valenciana

Publisher

Wiley

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