TY - JOUR
T1 - A conductive MXene hydrogel reprograms immunity and autophagy to restore neurovascular repair in infected wounds
AU - Xiao, Yuanhui
AU - Wu, Qingting
AU - Zeng, Chunping
AU - Li, Yanyou
AU - Wang, Kai
AU - Peng, Ziyu
AU - Luo, Yuner
AU - Wang, Zixi
AU - Huang, Lichun
AU - Huang, Shanshan
AU - Tang, Daolin
AU - Zhang, Baoliang
AU - Zhang, Qiuyu
AU - Liu, Jinbao
AU - Zhou, Li
N1 - Publisher Copyright:
© The Author(s) 2026. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2026
Y1 - 2026
N2 - Multidrug-resistant bacteria-infected wounds are difficult to heal due to persistent infection, excessive inflammation, impaired angiogenesis and deficient cutaneous innervation. Here, we develop an antibacterial and conductive bioactive hydrogel based on flower-shaped MXene microspheres for treating methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds. The hydrogel (PDM) is constructed by integrating ε-poly-L-lysine-functionalized MXene microspheres into a dynamically crosslinked oxidized pullulan network via pH-responsive Schiff-base chemistry, conferring injectability, self-healing, tissue adhesion and environmental responsiveness. PDM effectively eliminates MRSA biofilms, scavenges reactive oxygen species and attenuates inflammatory responses while promoting adaptive autophagy. These combined properties enable modulation of the wound microenvironment, enhance macrophage polarization toward a regenerative phenotype and support cell proliferation, endothelial cell migration and angiogenesis. In addition, the conductive hydrogel promotes Schwann cell maturation and neurotrophic factor expression, facilitating reconstruction of the neurogenic microenvironment. In a murine full-thickness MRSA-infected wound model, a single application of PDM significantly accelerates wound closure, enhances cutaneous innervation and reduces fibrosis. This work presents a multifunctional MXene-based hydrogel platform for antibiotic-free infected wound healing.
AB - Multidrug-resistant bacteria-infected wounds are difficult to heal due to persistent infection, excessive inflammation, impaired angiogenesis and deficient cutaneous innervation. Here, we develop an antibacterial and conductive bioactive hydrogel based on flower-shaped MXene microspheres for treating methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds. The hydrogel (PDM) is constructed by integrating ε-poly-L-lysine-functionalized MXene microspheres into a dynamically crosslinked oxidized pullulan network via pH-responsive Schiff-base chemistry, conferring injectability, self-healing, tissue adhesion and environmental responsiveness. PDM effectively eliminates MRSA biofilms, scavenges reactive oxygen species and attenuates inflammatory responses while promoting adaptive autophagy. These combined properties enable modulation of the wound microenvironment, enhance macrophage polarization toward a regenerative phenotype and support cell proliferation, endothelial cell migration and angiogenesis. In addition, the conductive hydrogel promotes Schwann cell maturation and neurotrophic factor expression, facilitating reconstruction of the neurogenic microenvironment. In a murine full-thickness MRSA-infected wound model, a single application of PDM significantly accelerates wound closure, enhances cutaneous innervation and reduces fibrosis. This work presents a multifunctional MXene-based hydrogel platform for antibiotic-free infected wound healing.
KW - autophagy
KW - cutaneous innervation
KW - immunomodulation
KW - MRSA-infected wound healing
KW - MXene microspheres hydrogel
UR - https://www.scopus.com/pages/publications/105043863908
U2 - 10.1093/rb/rbag108
DO - 10.1093/rb/rbag108
M3 - 文章
AN - SCOPUS:105043863908
SN - 2056-3418
VL - 13
JO - Regenerative Biomaterials
JF - Regenerative Biomaterials
M1 - rbag108
ER -