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Aggregation-Induced Emission Luminogens for Cell Death Research

[Image: see text] Cell death is closely related to various diseases, and monitoring and controlling cell death is a promising strategy to develop efficient therapy. Aggregation-induced emission luminogens (AIEgens) are ideal candidates for developing novel theranostic agents because of their intrigu...

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Autores principales: Zuo, Yunfei, Shen, Hanchen, Sun, Feiyi, Li, Pei, Sun, Jianwei, Kwok, Ryan T. K., Lam, Jacky W. Y., Tang, Ben Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114857/
https://www.ncbi.nlm.nih.gov/pubmed/37101570
http://dx.doi.org/10.1021/acsbiomedchemau.1c00066
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author Zuo, Yunfei
Shen, Hanchen
Sun, Feiyi
Li, Pei
Sun, Jianwei
Kwok, Ryan T. K.
Lam, Jacky W. Y.
Tang, Ben Zhong
author_facet Zuo, Yunfei
Shen, Hanchen
Sun, Feiyi
Li, Pei
Sun, Jianwei
Kwok, Ryan T. K.
Lam, Jacky W. Y.
Tang, Ben Zhong
author_sort Zuo, Yunfei
collection PubMed
description [Image: see text] Cell death is closely related to various diseases, and monitoring and controlling cell death is a promising strategy to develop efficient therapy. Aggregation-induced emission luminogens (AIEgens) are ideal candidates for developing novel theranostic agents because of their intriguing properties in the aggregate state. The rational application of AIE materials in cell death-related research is still in its infancy but has shown great clinical potential. This review discussed the research frontier and our understanding of AIE materials in various subroutines of cell death, including apoptosis, necrosis, immunogenic cell death, pyroptosis, autophagy, lysosome-dependent cell death, and ferroptosis. We hope that the new insights can be offered to this growing field and attract more researchers to provide valuable contributions.
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spelling pubmed-101148572023-04-25 Aggregation-Induced Emission Luminogens for Cell Death Research Zuo, Yunfei Shen, Hanchen Sun, Feiyi Li, Pei Sun, Jianwei Kwok, Ryan T. K. Lam, Jacky W. Y. Tang, Ben Zhong ACS Bio Med Chem Au [Image: see text] Cell death is closely related to various diseases, and monitoring and controlling cell death is a promising strategy to develop efficient therapy. Aggregation-induced emission luminogens (AIEgens) are ideal candidates for developing novel theranostic agents because of their intriguing properties in the aggregate state. The rational application of AIE materials in cell death-related research is still in its infancy but has shown great clinical potential. This review discussed the research frontier and our understanding of AIE materials in various subroutines of cell death, including apoptosis, necrosis, immunogenic cell death, pyroptosis, autophagy, lysosome-dependent cell death, and ferroptosis. We hope that the new insights can be offered to this growing field and attract more researchers to provide valuable contributions. American Chemical Society 2022-02-24 /pmc/articles/PMC10114857/ /pubmed/37101570 http://dx.doi.org/10.1021/acsbiomedchemau.1c00066 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Zuo, Yunfei
Shen, Hanchen
Sun, Feiyi
Li, Pei
Sun, Jianwei
Kwok, Ryan T. K.
Lam, Jacky W. Y.
Tang, Ben Zhong
Aggregation-Induced Emission Luminogens for Cell Death Research
title Aggregation-Induced Emission Luminogens for Cell Death Research
title_full Aggregation-Induced Emission Luminogens for Cell Death Research
title_fullStr Aggregation-Induced Emission Luminogens for Cell Death Research
title_full_unstemmed Aggregation-Induced Emission Luminogens for Cell Death Research
title_short Aggregation-Induced Emission Luminogens for Cell Death Research
title_sort aggregation-induced emission luminogens for cell death research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114857/
https://www.ncbi.nlm.nih.gov/pubmed/37101570
http://dx.doi.org/10.1021/acsbiomedchemau.1c00066
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