Mesenchymal stem cell-loaded hydrogel to inhibit inflammatory reaction in surgical brain injury via mitochondria transfer

IF 10.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of Controlled Release Pub Date : 2024-10-15 DOI:10.1016/j.jconrel.2024.09.051
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Abstract

Neurosurgical procedures are the key therapeutic interventions for the cerebral hemorrhage and brain tumors. However, neurosurgical procedures inevitably cause surgical brain injury (SBI), which will induce hemorrhage and inflammation. Gelatin Sponges are still the primary hemostatic materials used in clinical, but their anti-inflammatory efficacy is poor. Herein, we developed a cross-linked gelatin hydrogel (GelMA) to load mesenchymal stem cells (MSC) and directly implant them to the SBI site. Upon contacting the SBI site, the GelMA showed better clotting performance than Gelatin Sponges. Moreover, the MSC can reduce oxidative stress and enhance mitochondrial fusion via mitochondria transfer, resulting in ameliorating mitochondrial damage and reducing inflammation. Thus, the GelMA containing MSC can effectively reduce brain edema and inflammation and improve neurological function in SBI mouse models. In addition, GelMA exhibits excellent hemocompatibility and low cytotoxicity. It also enhances the proliferation of MSCs and decelerates the rapid depletion of MSCs. Therefore, MSC-loaded GelMA exhibits excellent hemostatic and anti-inflammatory effects, making it a potential new-generation biomaterial for SBI.
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间充质干细胞水凝胶通过线粒体转移抑制外科脑损伤的炎症反应。
神经外科手术是脑出血和脑肿瘤的主要治疗手段。然而,神经外科手术不可避免地会造成手术性脑损伤(SBI),从而诱发出血和炎症。明胶海绵仍是临床上使用的主要止血材料,但其抗炎效果较差。在此,我们开发了一种交联明胶水凝胶(GelMA),用于装载间充质干细胞(MSC)并将其直接植入 SBI 损伤部位。与明胶海绵相比,GelMA在接触SBI部位后显示出更好的凝血性能。此外,间充质干细胞还能减少氧化应激,并通过线粒体转移增强线粒体融合,从而改善线粒体损伤并减轻炎症。因此,含有间充质干细胞的 GelMA 能有效减轻 SBI 小鼠模型的脑水肿和炎症,改善神经功能。此外,GelMA 还具有良好的血液相容性和低细胞毒性。它还能促进间充质干细胞的增殖,减缓间充质干细胞的快速耗竭。因此,间充质干细胞负载的凝胶MA具有出色的止血和抗炎效果,是一种潜在的用于SBI的新一代生物材料。
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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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