Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healing

Abstract Various therapies have been utilized for treating diabetic wounds, yet current regiments do not simultaneously address the key intrinsic causes of slow wound healing, i.e., abnormal skin cell functions (particularly migration), delayed angiogenesis, and chronic inflammation. To address this...

Full description

Bibliographic Details
Main Authors: Hong Niu, Ya Guan, Ting Zhong, Liang Ma, Mohamed Zayed, Jianjun Guan
Format: Article
Language:English
Published: Nature Portfolio 2023-07-01
Series:npj Regenerative Medicine
Online Access:https://doi.org/10.1038/s41536-023-00313-3
_version_ 1797784793294831616
author Hong Niu
Ya Guan
Ting Zhong
Liang Ma
Mohamed Zayed
Jianjun Guan
author_facet Hong Niu
Ya Guan
Ting Zhong
Liang Ma
Mohamed Zayed
Jianjun Guan
author_sort Hong Niu
collection DOAJ
description Abstract Various therapies have been utilized for treating diabetic wounds, yet current regiments do not simultaneously address the key intrinsic causes of slow wound healing, i.e., abnormal skin cell functions (particularly migration), delayed angiogenesis, and chronic inflammation. To address this clinical gap, we develop a wound dressing that contains a peptide-based TGFβ receptor II inhibitor (PTβR2I), and a thermosensitive and reactive oxygen species (ROS)-scavenging hydrogel. The wound dressing can quickly solidify on the diabetic wounds following administration. The released PTβR2I inhibits the TGFβ1/p38 pathway, leading to improved cell migration and angiogenesis, and decreased inflammation. Meanwhile, the PTβR2I does not interfere with the TGFβ1/Smad2/3 pathway that is required to regulate myofibroblasts, a critical cell type for wound healing. The hydrogel’s ability to scavenge ROS in diabetic wounds further decreases inflammation. Single-dose application of the wound dressing significantly accelerates wound healing with complete wound closure after 14 days. Overall, using wound dressings capable of adaptively modulating TGFβ pathways provides a new strategy for diabetic wound treatment.
first_indexed 2024-03-13T00:44:56Z
format Article
id doaj.art-d2c0ad453c4f41fa86cdd828b8e05d5a
institution Directory Open Access Journal
issn 2057-3995
language English
last_indexed 2024-03-13T00:44:56Z
publishDate 2023-07-01
publisher Nature Portfolio
record_format Article
series npj Regenerative Medicine
spelling doaj.art-d2c0ad453c4f41fa86cdd828b8e05d5a2023-07-09T11:08:23ZengNature Portfolionpj Regenerative Medicine2057-39952023-07-018111910.1038/s41536-023-00313-3Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healingHong Niu0Ya Guan1Ting Zhong2Liang Ma3Mohamed Zayed4Jianjun Guan5Department of Mechanical Engineering and Materials Science, Washington University in St. LouisDepartment of Mechanical Engineering and Materials Science, Washington University in St. LouisDepartment of Mechanical Engineering and Materials Science, Washington University in St. LouisDepartment of Internal Medicine, Washington University School of MedicineDepartment of Surgery, Section of Vascular Surgery, Washington University School of MedicineDepartment of Mechanical Engineering and Materials Science, Washington University in St. LouisAbstract Various therapies have been utilized for treating diabetic wounds, yet current regiments do not simultaneously address the key intrinsic causes of slow wound healing, i.e., abnormal skin cell functions (particularly migration), delayed angiogenesis, and chronic inflammation. To address this clinical gap, we develop a wound dressing that contains a peptide-based TGFβ receptor II inhibitor (PTβR2I), and a thermosensitive and reactive oxygen species (ROS)-scavenging hydrogel. The wound dressing can quickly solidify on the diabetic wounds following administration. The released PTβR2I inhibits the TGFβ1/p38 pathway, leading to improved cell migration and angiogenesis, and decreased inflammation. Meanwhile, the PTβR2I does not interfere with the TGFβ1/Smad2/3 pathway that is required to regulate myofibroblasts, a critical cell type for wound healing. The hydrogel’s ability to scavenge ROS in diabetic wounds further decreases inflammation. Single-dose application of the wound dressing significantly accelerates wound healing with complete wound closure after 14 days. Overall, using wound dressings capable of adaptively modulating TGFβ pathways provides a new strategy for diabetic wound treatment.https://doi.org/10.1038/s41536-023-00313-3
spellingShingle Hong Niu
Ya Guan
Ting Zhong
Liang Ma
Mohamed Zayed
Jianjun Guan
Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healing
npj Regenerative Medicine
title Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healing
title_full Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healing
title_fullStr Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healing
title_full_unstemmed Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healing
title_short Thermosensitive and antioxidant wound dressings capable of adaptively regulating TGFβ pathways promote diabetic wound healing
title_sort thermosensitive and antioxidant wound dressings capable of adaptively regulating tgfβ pathways promote diabetic wound healing
url https://doi.org/10.1038/s41536-023-00313-3
work_keys_str_mv AT hongniu thermosensitiveandantioxidantwounddressingscapableofadaptivelyregulatingtgfbpathwayspromotediabeticwoundhealing
AT yaguan thermosensitiveandantioxidantwounddressingscapableofadaptivelyregulatingtgfbpathwayspromotediabeticwoundhealing
AT tingzhong thermosensitiveandantioxidantwounddressingscapableofadaptivelyregulatingtgfbpathwayspromotediabeticwoundhealing
AT liangma thermosensitiveandantioxidantwounddressingscapableofadaptivelyregulatingtgfbpathwayspromotediabeticwoundhealing
AT mohamedzayed thermosensitiveandantioxidantwounddressingscapableofadaptivelyregulatingtgfbpathwayspromotediabeticwoundhealing
AT jianjunguan thermosensitiveandantioxidantwounddressingscapableofadaptivelyregulatingtgfbpathwayspromotediabeticwoundhealing