Affiliation:
1. Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 P. R. China
2. Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials Department of Orthopaedics the Second Affiliated Hospital of Jiaxing University Jiaxing 314000 China
3. ENT Institute Department of Facial Plastic and Reconstructive Surgery Eye & ENT Hospital Fudan University Shanghai 200031 China
Abstract
AbstractExcessive cell‐free DNA (cfDNA) can induce chronic inflammation by activating intracellular nucleic acid sensors. Intervention in cfDNA‐mediated “pro‐inflammatory signaling transduction” could be a potential alleviating strategy for chronic inflammation, such as in diabetic wounds. However, effectively and specifically downgrading cfDNA concentration in the pathological microenvironment remains a challenge. Therefore, this work prepares free‐standing polydopamine nanosheets through DNA‐guided assembly and loaded them into microfluidic hydrogel microspheres. The π─π stacking/hydrogen bonding interactions between polydopamine nanosheets and the π‐rich bases of cfDNA, along with the cage‐like spatial confinement created by the hydrogel polymer network, achieved cfDNA capture and storage, respectively. Catechol in polydopamine nanosheets can also assist in reducing reactive oxygen species (ROS) levels. Efficient cfDNA binding independent of serum proteins, specific interdiction of abnormal activation of cfDNA‐associated toll‐like receptor 9, as well as down‐regulation of inflammatory cytokines and ROS levels are shown in this system. The chronic inflammation alleviating and the pro‐healing effects on the mice model with diabetic wounds are also investigated. This work presents a new strategy for capturing and storing cfDNA to intervene in cell signaling transduction. It also offers new insights into the regulatory mechanisms between inflammatory mediators and biomaterials in inflammation‐related diseases.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
China Postdoctoral Science Foundation
Science and Technology Commission of Shanghai Municipality