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通过调节巨噬细胞极化作用,使用硫酸软骨素锂水凝胶促进糖尿病骨再生。

Using chondroitin sulfate lithium hydrogel for diabetic bone regeneration via regulation of macrophage polarization.

机构信息

Department of Oral and Cranio-maxillofacial Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, College of Stomatology, Shanghai Jiao Tong University, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Key Laboratory of Stomatology, Shanghai Research Institute of Stomatology, Shanghai 200011, China.

Department of Obstetrics, Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University, Shanghai 200092, China.

出版信息

Carbohydr Polym. 2025 Jan 1;347:122787. doi: 10.1016/j.carbpol.2024.122787. Epub 2024 Sep 22.

Abstract

Bone regeneration in a diabetic environment remains a clinical challenge because of the proinflammatory microenvironment and malfunction of osteogenesis. Traditional therapy for bone defects doesn't work out in diabetes. Therefore, we introduced lithium (Li) into chondroitin sulfate (CS) and developed a crosslinked hydrogel composed of gelatin methacryloyl (GelMA) and chondroitin sulfate lithium (CS-Li) which could release Li in a sustained manner. This crosslinked hydrogel has a porous microstructure, excellent biocompatibility, and osteogenesis properties. With the synergetic effects of CS and Li, this crosslinked hydrogel regulates macrophage polarization to anti-inflammatory phenotype in the high glucose microenvironment and alleviates the inhibition of angiogenesis and osteogenesis caused by diabetes both in vitro and in vivo. The relationship between macrophage polarization and the promotion of angiogenesis and osteogenesis in diabetic microenvironments may be attributed to the activation of Glycogen synthase kinase-3β/β-catenin pathways. Overall, significant results in this study present that CS-Li was a potential therapy for bone defects in diabetic patients.

摘要

糖尿病环境中的骨再生仍然是一个临床挑战,因为其存在促炎微环境和成骨功能障碍。传统的骨缺损治疗方法在糖尿病中并不适用。因此,我们将锂 (Li) 引入到硫酸软骨素 (CS) 中,并开发了一种由明胶甲基丙烯酰 (GelMA) 和硫酸软骨素锂 (CS-Li) 组成的交联水凝胶,其可以持续释放 Li。这种交联水凝胶具有多孔的微观结构、优异的生物相容性和成骨性能。通过 CS 和 Li 的协同作用,这种交联水凝胶可将巨噬细胞极化为高糖微环境中的抗炎表型,并减轻糖尿病在体外和体内对血管生成和成骨的抑制。巨噬细胞极化与促进糖尿病微环境中的血管生成和成骨之间的关系可能归因于糖原合酶激酶-3β/β-连环蛋白途径的激活。总的来说,这项研究中的显著结果表明 CS-Li 可能是糖尿病患者骨缺损的一种潜在治疗方法。

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