Customized Proteinaceous Nanoformulation for In Vivo Chemical Reprogramming

Sweat gland (SwG) regeneration is crucial for the functional rehabilitation of burn patients. In vivo chemical reprogramming that harnessing the patient's own cells in damaged tissue is of substantial interest to regenerate organs endogenously by pharmacological manipulation, which could compen...

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Veröffentlicht in:Advanced materials (Weinheim) 2024-07, Vol.36 (28), p.e2311845-n/a
Hauptverfasser: Chen, Huating, Xiang, Jiangbing, Liu, Yawei, Pi, Wei, Zhang, Hongliang, Wu, Lu, Liu, Yiqiong, Ji, Shuaifei, Li, Yan, Cui, Shaoyuan, Liu, Kai, Fu, Xiaobing, Sun, Xiaoyan
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container_start_page e2311845
container_title Advanced materials (Weinheim)
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creator Chen, Huating
Xiang, Jiangbing
Liu, Yawei
Pi, Wei
Zhang, Hongliang
Wu, Lu
Liu, Yiqiong
Ji, Shuaifei
Li, Yan
Cui, Shaoyuan
Liu, Kai
Fu, Xiaobing
Sun, Xiaoyan
description Sweat gland (SwG) regeneration is crucial for the functional rehabilitation of burn patients. In vivo chemical reprogramming that harnessing the patient's own cells in damaged tissue is of substantial interest to regenerate organs endogenously by pharmacological manipulation, which could compensate for tissue loss in devastating diseases and injuries, for example, burns. However, achieving in vivo chemical reprogramming is challenging due to the low reprogramming efficiency and an unfavorable tissue environment. Herein, this work has developed a functionalized proteinaceous nanoformulation delivery system containing prefabricated epidermal growth factor structure for on‐demand delivery of a cocktail of seven SwG reprogramming components to the dermal site. Such a chemical reprogramming system can efficiently induce the conversion of epidermal keratinocytes into SwG myoepithelial cells, resulting in successful in situ regeneration of functional SwGs. Notably, in vivo chemical reprogramming of SwGs is achieved for the first time with an impressive efficiency of 30.6%, surpassing previously reported efficiencies. Overall, this proteinaceous nanoformulation provides a platform for coordinating the target delivery of multiple pharmacological agents and facilitating in vivo SwG reprogramming by chemicals. This advancement greatly improves the clinical accessibility of in vivo reprogramming and offers a non‐surgical, non‐viral, and cell‐free strategy for in situ SwG regeneration. This work has developed the functional proteinaceous nanoformulation for on‐demand co‐delivery of multiple pharmacological reprogramming factors, which selectively reprogram keratinocytes into myoepithelial cells and achieve de novo regeneration of functional sweat glands in vivo and in situ. This work shows the highest in vivo chemical reprogramming efficiency and offers a transgene‐free and clinically adaptable approach for burn treatment with improved rehabilitation.
doi_str_mv 10.1002/adma.202311845
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In vivo chemical reprogramming that harnessing the patient's own cells in damaged tissue is of substantial interest to regenerate organs endogenously by pharmacological manipulation, which could compensate for tissue loss in devastating diseases and injuries, for example, burns. However, achieving in vivo chemical reprogramming is challenging due to the low reprogramming efficiency and an unfavorable tissue environment. Herein, this work has developed a functionalized proteinaceous nanoformulation delivery system containing prefabricated epidermal growth factor structure for on‐demand delivery of a cocktail of seven SwG reprogramming components to the dermal site. Such a chemical reprogramming system can efficiently induce the conversion of epidermal keratinocytes into SwG myoepithelial cells, resulting in successful in situ regeneration of functional SwGs. Notably, in vivo chemical reprogramming of SwGs is achieved for the first time with an impressive efficiency of 30.6%, surpassing previously reported efficiencies. Overall, this proteinaceous nanoformulation provides a platform for coordinating the target delivery of multiple pharmacological agents and facilitating in vivo SwG reprogramming by chemicals. This advancement greatly improves the clinical accessibility of in vivo reprogramming and offers a non‐surgical, non‐viral, and cell‐free strategy for in situ SwG regeneration. This work has developed the functional proteinaceous nanoformulation for on‐demand co‐delivery of multiple pharmacological reprogramming factors, which selectively reprogram keratinocytes into myoepithelial cells and achieve de novo regeneration of functional sweat glands in vivo and in situ. 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In vivo chemical reprogramming that harnessing the patient's own cells in damaged tissue is of substantial interest to regenerate organs endogenously by pharmacological manipulation, which could compensate for tissue loss in devastating diseases and injuries, for example, burns. However, achieving in vivo chemical reprogramming is challenging due to the low reprogramming efficiency and an unfavorable tissue environment. Herein, this work has developed a functionalized proteinaceous nanoformulation delivery system containing prefabricated epidermal growth factor structure for on‐demand delivery of a cocktail of seven SwG reprogramming components to the dermal site. Such a chemical reprogramming system can efficiently induce the conversion of epidermal keratinocytes into SwG myoepithelial cells, resulting in successful in situ regeneration of functional SwGs. Notably, in vivo chemical reprogramming of SwGs is achieved for the first time with an impressive efficiency of 30.6%, surpassing previously reported efficiencies. Overall, this proteinaceous nanoformulation provides a platform for coordinating the target delivery of multiple pharmacological agents and facilitating in vivo SwG reprogramming by chemicals. This advancement greatly improves the clinical accessibility of in vivo reprogramming and offers a non‐surgical, non‐viral, and cell‐free strategy for in situ SwG regeneration. This work has developed the functional proteinaceous nanoformulation for on‐demand co‐delivery of multiple pharmacological reprogramming factors, which selectively reprogram keratinocytes into myoepithelial cells and achieve de novo regeneration of functional sweat glands in vivo and in situ. 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Notably, in vivo chemical reprogramming of SwGs is achieved for the first time with an impressive efficiency of 30.6%, surpassing previously reported efficiencies. Overall, this proteinaceous nanoformulation provides a platform for coordinating the target delivery of multiple pharmacological agents and facilitating in vivo SwG reprogramming by chemicals. This advancement greatly improves the clinical accessibility of in vivo reprogramming and offers a non‐surgical, non‐viral, and cell‐free strategy for in situ SwG regeneration. This work has developed the functional proteinaceous nanoformulation for on‐demand co‐delivery of multiple pharmacological reprogramming factors, which selectively reprogram keratinocytes into myoepithelial cells and achieve de novo regeneration of functional sweat glands in vivo and in situ. This work shows the highest in vivo chemical reprogramming efficiency and offers a transgene‐free and clinically adaptable approach for burn treatment with improved rehabilitation.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38720198</pmid><doi>10.1002/adma.202311845</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-0878-5191</orcidid></addata></record>
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subjects Animals
Cellular Reprogramming - drug effects
Chemical damage
chemical reprogramming
cocktail nanoformulation
Epidermal Growth Factor - chemistry
Epidermal Growth Factor - metabolism
Epidermal Growth Factor - pharmacology
Growth factors
Humans
in situ sweat gland regeneration
Keratinocytes - cytology
Keratinocytes - drug effects
Keratinocytes - metabolism
Mice
Nanoparticles - chemistry
on‐demand delivery
Pharmacology
Prefabricated buildings
protein engineering
Regeneration
Regeneration - drug effects
title Customized Proteinaceous Nanoformulation for In Vivo Chemical Reprogramming
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