Surface-fill H2S-releasing silk fibroin hydrogel for brain repair through the repression of neuronal pyroptosis

被引:44
作者
Chen, Xueshi [1 ]
Huang, Xinqi [1 ]
Liu, Chao [2 ,5 ]
Li, Sunao [1 ]
Yang, Zhenbei [3 ]
Zhang, Feng [3 ]
Chen, Xiping [1 ]
Shan, Haiyan [4 ]
Tao, Luyang [1 ]
Zhang, Mingyang [1 ]
机构
[1] Soochow Univ, Sch Basic Med & Biol Sci, Dept Forens Med, Suzhou Med Coll, Suzhou 215123, Peoples R China
[2] Soochow Univ, Dept Orthoped, Affiliated Hosp 2, Suzhou 215123, Peoples R China
[3] Soochow Univ, Coll Text & Clothing Engn, Natl Engn Lab Modern Silk, Suzhou 215123, Peoples R China
[4] Nanjing Med Univ, Dept Obstet & Gynecol, Affiliated Suzhou Hosp, Suzhou 215123, Peoples R China
[5] Nanjing Med Univ, Suzhou BenQ Med Ctr, Dept Orthoped, Affiliated BenQ Hosp, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Traumatic brain injury; Silk fibroin hydrogel; Hydrogen sulfide; Pyroptosis; Necroptosis; CYSTATHIONINE-BETA-SYNTHASE; GASDERMIN D; MOUSE MODEL; INFLAMMATORY CASPASES; IN-VITRO; INJURY; SULFIDE; NEUROINFLAMMATION; ACTIVATION; INHIBITOR;
D O I
10.1016/j.actbio.2022.11.021
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Traumatic brain injury (TBI) remains the major cause of disability and mortality worldwide due to the persistent neuroinflammation and neuronal death induced by TBI. Among them, pyroptosis, a specific type of programmed cell death (PCD) triggered by inflammatory signals, plays a significant part in the pathological process after TBI. Inhibition of neuroinflammation and pyroptosis is considered a possible strategy for the treatment of TBI. In our previous study, exogenous hydrogen sulfide(H2S) exerted a neu-roprotective effect after TBI. Here, we developed a surface-fill H2S-releasing silk fibroin (SF) hydrogel (H2S@SF hydrogel) to achieve small-dose local administration and avoid volatile and toxic side effects. We used a controlled cortical impact (CCI) to establish a mild TBI model in mice to examine the effect of H2S@SF hydrogel on TBI-induced pyroptosis. We found that H2S@SF hydrogel inhibited the expres-sion of H2S synthase in neurons after TBI and significantly inhibited TBI-induced neuronal pyroptosis. In addition, immunofluorescence staining results showed that the necroptosis protein receptor-interacting serine/threonine-protein kinase 1 (RIPK1) partially colocalized with the pyroptosis protein Gasdermin D (GSDMD) in the same cells. H2S@SF hydrogel can also inhibit the expression of the necroptosis protein. Moreover, H2S@SF hydrogel also alleviates brain edema and the degree of neurodegeneration in the acute phase of TBI. The neuroprotective effect of H2S@SF hydrogel was further confirmed by wire-grip test, open field test, Morris water maze, beam balance test, radial arm maze, tail suspension, and forced swimming test. Lastly, we also measured spared tissue volume, reactive astrocytes and activated microglia to demon-strate H2S@SF hydrogel impacts on long-term prognosis in TBI. Our study provides a new theoretical basis for the treatment of H2S after TBI and the clinical application of H2S@SF hydrogel. Statement of significance Silk fibroin (SF) hydrogel controls the release of hydrogen sulfide (H 2 S) to inhibit neuronal pyroptosis and neuroinflammation in injured brain tissue. In this study, we synthesized a surface-fill H2S-releasing silk fibroin hydrogel, which could slowly release H2S to reshape the homeostasis of endogenous H2S in injured neurons and inhibit neuronal pyroptosis in a mouse model of traumatic brain injury. Meanwhile, H2S@SF hydrogel could alleviate brain edema and the degree of neurodegeneration, improve motor dys-function, anxious behavior and memory impairment caused by TBI, reduce tissue loss and ameliorate neuroinflammation. Our study provides a new theoretical basis for the treatment of H2S after TBI and the clinical application of H2S@SF hydrogel. (c) 2022 The Author(s). Published by Elsevier Ltd on behalf of Acta Materialia Inc. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页码:259 / 274
页数:16
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