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A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo

Senescent cells (SnCs) are implicated in aging and various age‐related pathologies. Targeting SnCs can treat age‐related diseases and extend health span. However, precisely tracking and visualizing of SnCs is still challenging, especially in in vivo environments. Here, we developed a near‐infrared (...

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Autores principales: Hu, Li, Dong, Chanjuan, Wang, Zhe, He, Shengyuan, Yang, Yiwen, Zi, Meiting, Li, Huiqin, Zhang, Yanghuan, Chen, Chuanjie, Zheng, Runzi, Jia, Shuting, Liu, Jing, Zhang, Xuan, He, Yonghan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410003/
https://www.ncbi.nlm.nih.gov/pubmed/37312431
http://dx.doi.org/10.1111/acel.13896
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author Hu, Li
Dong, Chanjuan
Wang, Zhe
He, Shengyuan
Yang, Yiwen
Zi, Meiting
Li, Huiqin
Zhang, Yanghuan
Chen, Chuanjie
Zheng, Runzi
Jia, Shuting
Liu, Jing
Zhang, Xuan
He, Yonghan
author_facet Hu, Li
Dong, Chanjuan
Wang, Zhe
He, Shengyuan
Yang, Yiwen
Zi, Meiting
Li, Huiqin
Zhang, Yanghuan
Chen, Chuanjie
Zheng, Runzi
Jia, Shuting
Liu, Jing
Zhang, Xuan
He, Yonghan
author_sort Hu, Li
collection PubMed
description Senescent cells (SnCs) are implicated in aging and various age‐related pathologies. Targeting SnCs can treat age‐related diseases and extend health span. However, precisely tracking and visualizing of SnCs is still challenging, especially in in vivo environments. Here, we developed a near‐infrared (NIR) fluorescent probe (XZ1208) that targets β‐galactosidase (β‐Gal), a well‐accepted biomarker for cellular senescence. XZ1208 can be cleaved rapidly by β‐Gal and produces a strong fluorescence signal in SnCs. We demonstrated the high specificity and sensitivity of XZ1208 in labeling SnCs in naturally aged, total body irradiated (TBI), and progeroid mouse models. XZ1208 achieved a long‐term duration of over 6 days in labeling senescence without causing significant toxicities and accurately detected the senolytic effects of ABT263 on eliminating SnCs. Furthermore, XZ1208 was applied to monitor SnCs accumulated in fibrotic diseases and skin wound healing models. Overall, we developed a tissue‐infiltrating NIR probe and demonstrated its excellent performance in labeling SnCs in aging and senescence‐associated disease models, indicating great potential for application in aging studies and diagnosis of senescence‐associated diseases.
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spelling pubmed-104100032023-08-10 A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo Hu, Li Dong, Chanjuan Wang, Zhe He, Shengyuan Yang, Yiwen Zi, Meiting Li, Huiqin Zhang, Yanghuan Chen, Chuanjie Zheng, Runzi Jia, Shuting Liu, Jing Zhang, Xuan He, Yonghan Aging Cell Research Articles Senescent cells (SnCs) are implicated in aging and various age‐related pathologies. Targeting SnCs can treat age‐related diseases and extend health span. However, precisely tracking and visualizing of SnCs is still challenging, especially in in vivo environments. Here, we developed a near‐infrared (NIR) fluorescent probe (XZ1208) that targets β‐galactosidase (β‐Gal), a well‐accepted biomarker for cellular senescence. XZ1208 can be cleaved rapidly by β‐Gal and produces a strong fluorescence signal in SnCs. We demonstrated the high specificity and sensitivity of XZ1208 in labeling SnCs in naturally aged, total body irradiated (TBI), and progeroid mouse models. XZ1208 achieved a long‐term duration of over 6 days in labeling senescence without causing significant toxicities and accurately detected the senolytic effects of ABT263 on eliminating SnCs. Furthermore, XZ1208 was applied to monitor SnCs accumulated in fibrotic diseases and skin wound healing models. Overall, we developed a tissue‐infiltrating NIR probe and demonstrated its excellent performance in labeling SnCs in aging and senescence‐associated disease models, indicating great potential for application in aging studies and diagnosis of senescence‐associated diseases. John Wiley and Sons Inc. 2023-06-13 /pmc/articles/PMC10410003/ /pubmed/37312431 http://dx.doi.org/10.1111/acel.13896 Text en © 2023 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Hu, Li
Dong, Chanjuan
Wang, Zhe
He, Shengyuan
Yang, Yiwen
Zi, Meiting
Li, Huiqin
Zhang, Yanghuan
Chen, Chuanjie
Zheng, Runzi
Jia, Shuting
Liu, Jing
Zhang, Xuan
He, Yonghan
A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo
title A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo
title_full A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo
title_fullStr A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo
title_full_unstemmed A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo
title_short A rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo
title_sort rationally designed fluorescence probe achieves highly specific and long‐term detection of senescence in vitro and in vivo
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410003/
https://www.ncbi.nlm.nih.gov/pubmed/37312431
http://dx.doi.org/10.1111/acel.13896
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