Novel fabrication of bioengineered injectable chitosan hydrogel loaded with conductive nanoparticles to improve therapeutic potential of mesenchymal stem cells in functional recovery after ischemic myocardial infarction

IF 4.7 4区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Nanomedicine: Nanotechnology, Biology and Medicine Pub Date : 2023-01-01 DOI:10.1016/j.nano.2022.102616
Zheng Wu Ph.D, Wenzheng Li Ph.D, Shujuan Cheng Ph.D, Jinghua Liu Ph.D, Shaoping Wang Ph.D
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引用次数: 6

Abstract

In recent decades, myocardial regeneration through stem cell transplantation and tissue engineering has been viewed as a promising technique for treating myocardial infarction. As a result, the researcher attempts to see whether co-culturing modified mesenchymal stem cells with Au@Ch-SF macro-hydrogel and H9C2 may help with tissue regeneration and cardiac function recovery. The gold nanoparticles (Au) incorporated into the chitosan-silk fibroin hydrogel (Au@Ch-SF) were validated using spectral and microscopic examinations. The most essential elements of hydrogel groups were investigated in detail, including weight loss, mechanical strength, and drug release rate. Initially, the cardioblast cells (H9C2 cells) was incubated with Au@Ch-SF macro-hydrogel, followed by mesenchymal stem cells (2 × 105) were transplanted into the Au@Ch-SF macro-hydrogel+H9C2 culture at the ratio of 2:1. Further, cardiac phenotype development, cytokines expression and tissue regenerative performance of modified mesenchymal stem cells treatment were studied through various in vitro and in vivo analyses. The Au@Ch-SF macro-hydrogel gelation time was much faster than that of Ch and Ch-SF hydrogels, showing that Ch and SF exhibited greater intermolecular interactions. The obtained Au@Ch-SF macro-hydrogel has no toxicity on mesenchymal stem cells (MS) or cardiac myoblast (H9C2) cells, according to the biocompatibility investigation. MS cells co-cultured with Au@Ch-SF macro-hydrogel and H9C2 cells also stimulated cardiomyocyte fiber restoration, which has been confirmed in myocardial infarction rats using -MHC and Cx43 myocardial indicators. We developed a novel method of co-cultured therapy using MS cells, Au@Ch-SF macro-hydrogel, and H9C2 cells which could promote the regenerative activities in myocardial ischemia cells. These study findings show that co-cultured MS therapy might be effective for the treatment of myocardial injury.

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载导电纳米颗粒的生物工程可注射壳聚糖水凝胶的新型制备提高间充质干细胞在缺血性心肌梗死后功能恢复中的治疗潜力
近几十年来,通过干细胞移植和组织工程进行心肌再生被认为是治疗心肌梗死的一种很有前途的技术。因此,研究人员试图观察与Au@Ch-SF大水凝胶和H9C2共培养修饰间充质干细胞是否有助于组织再生和心功能恢复。将金纳米颗粒(Au)掺入壳聚糖-丝素水凝胶(Au@Ch-SF)中,通过光谱和显微镜检查进行了验证。详细考察了水凝胶组的最基本元素,包括减重、机械强度和药物释放率。先将成心细胞(H9C2细胞)与Au@Ch-SF大水凝胶孵育,然后将2 × 105的间充质干细胞按2:1的比例移植到Au@Ch-SF大水凝胶+H9C2培养液中。此外,通过各种体外和体内分析,研究了改良间充质干细胞处理的心脏表型发育、细胞因子表达和组织再生性能。Au@Ch-SF宏观水凝胶凝胶化时间明显快于Ch和Ch-SF水凝胶,说明Ch和SF表现出更强的分子间相互作用。根据生物相容性调查,所得Au@Ch-SF大水凝胶对间充质干细胞(MS)或心肌母细胞(H9C2)细胞无毒性。MS细胞与Au@Ch-SF大水凝胶和H9C2细胞共培养也能刺激心肌细胞纤维的恢复,这在心肌梗死大鼠中已通过-MHC和Cx43心肌指标得到证实。研究了MS细胞、Au@Ch-SF大水凝胶和H9C2细胞共培养治疗心肌缺血细胞再生活性的新方法。这些研究结果表明,共培养MS治疗心肌损伤可能是有效的。
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来源期刊
CiteScore
8.10
自引率
3.60%
发文量
104
审稿时长
4.6 months
期刊介绍: Nanomedicine: Nanotechnology, Biology and Medicine (NBM) is an international, peer-reviewed journal presenting novel, significant, and interdisciplinary theoretical and experimental results related to nanoscience and nanotechnology in the life and health sciences. Content includes basic, translational, and clinical research addressing diagnosis, treatment, monitoring, prediction, and prevention of diseases.
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