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- Publisher Website: 10.1002/adfm.202316545
- Scopus: eid_2-s2.0-85189676003
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Article: Injectable Hydrogel Based on Enzymatic Initiation of Keratin Methacrylate for Controlled Exosome Release in Intervertebral Disc Degeneration Therapy
Title | Injectable Hydrogel Based on Enzymatic Initiation of Keratin Methacrylate for Controlled Exosome Release in Intervertebral Disc Degeneration Therapy |
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Authors | |
Keywords | anti-inflammation enzymatic cascade reaction extracellular matrix regeneration intervertebral disc degeneration mechanical support |
Issue Date | 8-Aug-2024 |
Publisher | Wiley |
Citation | Advanced Functional Materials, 2024, v. 34, n. 32 How to Cite? |
Abstract | The treatment of intervertebral disc degeneration (IVDD) using bone marrow mesenchymal stem cell-derived exosomes has shown success in alleviating inflammation and restoring the extracellular matrix (ECM), however, challenges persist due to the deficiency in mechanical support and controlled release. Herein, a carbon-carbon double bond modified keratin (KeMA) is synthesized by 2-isocyanatoethyl modification for exosomes wrapping. This injectable KeMA hydrogel, initiated by a biocompatible glucose/ glucose oxidase/ horse radish peroxidase enzymatic cascade reaction with acetylacetone and N-vinylpyrrolidone, displayed rapid gelation, resembling nucleus pulposus (NP) elasticity, and excellent cytocompatibility. In vitro studies showcased that the exosomes-loaded KeMA hydrogel (Exo@KeMA) enhanced exosome release kinetics, suppressed inflammation, fostered extracellular matrix (ECM) regeneration, and reinstated NP biomechanics. RNA-seq analysis indicated Exo@KeMA's effects involved PI3K-Akt signaling for matrix regeneration and NF-κB signaling inhibition for anti-inflammation. In vivo IVDD rat models demonstrated Exo@KeMA attenuated inflammation, maintained NP water content, preserved disc height, and promoted structural regeneration. This research introduces an injectable KeMA hydrogel as a promising therapy for IVDD, by facilitating biomechanics restoration, anti-inflammatory response, and ECM regeneration. |
Persistent Identifier | http://hdl.handle.net/10722/345644 |
ISSN | 2023 Impact Factor: 18.5 2023 SCImago Journal Rankings: 5.496 |
DC Field | Value | Language |
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dc.contributor.author | Chen, Linjie | - |
dc.contributor.author | Peng, Ke | - |
dc.contributor.author | Huang, He | - |
dc.contributor.author | Gong, Zehua | - |
dc.contributor.author | Huang, Jinyi | - |
dc.contributor.author | Mohamed, Abdihafid Mohamud | - |
dc.contributor.author | Chen, Qizhu | - |
dc.contributor.author | Sow, Wan Ting | - |
dc.contributor.author | Guo, Liting | - |
dc.contributor.author | Kwan, Kenny Yat Hong | - |
dc.contributor.author | Li, Bin | - |
dc.contributor.author | Khan, Moonis Ali | - |
dc.contributor.author | Makvnadi, Pooyan | - |
dc.contributor.author | Jones, Morgan | - |
dc.contributor.author | Shen, Shuying | - |
dc.contributor.author | Wang, Xiangyang | - |
dc.contributor.author | Ma, Chao | - |
dc.contributor.author | Li, Huaqiong | - |
dc.contributor.author | Wu, Aimin | - |
dc.date.accessioned | 2024-08-27T09:10:13Z | - |
dc.date.available | 2024-08-27T09:10:13Z | - |
dc.date.issued | 2024-08-08 | - |
dc.identifier.citation | Advanced Functional Materials, 2024, v. 34, n. 32 | - |
dc.identifier.issn | 1616-301X | - |
dc.identifier.uri | http://hdl.handle.net/10722/345644 | - |
dc.description.abstract | <p>The treatment of intervertebral disc degeneration (IVDD) using bone marrow mesenchymal stem cell-derived exosomes has shown success in alleviating inflammation and restoring the extracellular matrix (ECM), however, challenges persist due to the deficiency in mechanical support and controlled release. Herein, a carbon-carbon double bond modified keratin (KeMA) is synthesized by 2-isocyanatoethyl modification for exosomes wrapping. This injectable KeMA hydrogel, initiated by a biocompatible glucose/ glucose oxidase/ horse radish peroxidase enzymatic cascade reaction with acetylacetone and N-vinylpyrrolidone, displayed rapid gelation, resembling nucleus pulposus (NP) elasticity, and excellent cytocompatibility. In vitro studies showcased that the exosomes-loaded KeMA hydrogel (Exo@KeMA) enhanced exosome release kinetics, suppressed inflammation, fostered extracellular matrix (ECM) regeneration, and reinstated NP biomechanics. RNA-seq analysis indicated Exo@KeMA's effects involved PI3K-Akt signaling for matrix regeneration and NF-κB signaling inhibition for anti-inflammation. In vivo IVDD rat models demonstrated Exo@KeMA attenuated inflammation, maintained NP water content, preserved disc height, and promoted structural regeneration. This research introduces an injectable KeMA hydrogel as a promising therapy for IVDD, by facilitating biomechanics restoration, anti-inflammatory response, and ECM regeneration.</p> | - |
dc.language | eng | - |
dc.publisher | Wiley | - |
dc.relation.ispartof | Advanced Functional Materials | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | anti-inflammation | - |
dc.subject | enzymatic cascade reaction | - |
dc.subject | extracellular matrix regeneration | - |
dc.subject | intervertebral disc degeneration | - |
dc.subject | mechanical support | - |
dc.title | Injectable Hydrogel Based on Enzymatic Initiation of Keratin Methacrylate for Controlled Exosome Release in Intervertebral Disc Degeneration Therapy | - |
dc.type | Article | - |
dc.identifier.doi | 10.1002/adfm.202316545 | - |
dc.identifier.scopus | eid_2-s2.0-85189676003 | - |
dc.identifier.volume | 34 | - |
dc.identifier.issue | 32 | - |
dc.identifier.eissn | 1616-3028 | - |
dc.identifier.issnl | 1616-301X | - |