血液相容性核小体激发的模拟肝素水凝胶微球用于安全有效的体外清除危重患者循环组蛋白。

Yu Chen, Tinghang Yang, Shujing Wang, Dongmei Tong, Xianda Liu, Yupei Li, Weifeng Zhao, Changsheng Zhao
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引用次数: 0

摘要

循环组蛋白已被确定为导致脓毒症、多发性创伤、COVID-19、急性肝衰竭和胰腺炎重症患者的高炎症、血小板聚集、凝血级联激活、内皮细胞损伤、多器官功能障碍和死亡的重要介质。临床证据表明,血浆循环组蛋白水平与这些危重疾病患者的疾病严重程度和生存呈正相关。然而,在目前的临床实践中,缺乏针对循环组蛋白的安全有效的治疗策略。体外血液净化是一种广泛应用于重症监护病房的生命维持技术,是消除循环组蛋白的一种有前途的治疗选择。受自然核小体中DNA链和组蛋白之间静电相互作用的启发,我们提出了一种“一石二鸟”的策略,通过开发模拟肝素的水凝胶微球(RCHMs)来对抗组蛋白相关的关键疾病。一方面,通过原位交联聚合,RCHMs内部的模拟肝素的水凝胶结构含有大量的羧基和磺酸基,这使得RCHMs具有优异的血液相容性。另一方面,RCHMs可以通过静电相互作用吸附循环组蛋白。我们的研究结果表明,RCHMs不会引起明显的溶血,血细胞活化和补体活化,具有更好的抗蛋白质污染特性。定制的RCHM微球(A3M1)在4 h内可高效、选择性地吸附91.16%的小牛胸腺组蛋白,吸附量为20.47 μg mg-1。RCHM可显著减轻组蛋白介导的血小板减少、血小板聚集和内皮细胞死亡。因此,rchm是一种有前途的血液灌流吸附剂,可用于体外清除危重患者血液中的循环组蛋白,为多种组蛋白相关疾病的治疗提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hemocompatible nucleosome-inspired heparin-mimicking hydrogel microspheres for safe and efficient extracorporeal removal of circulating histones in critically ill patients.

Circulating histones have been identified as essential mediators that lead to hyperinflammation, platelet aggregation, coagulation cascade activation, endothelial cell injury, multiple organ dysfunction, and death in severe patients with sepsis, multiple trauma, COVID-19, acute liver failure, and pancreatitis. Clinical evidence suggests that plasma levels of circulating histones are positively associated with disease severity and survival in patients with such critical diseases. However, safe and efficient therapeutic strategies targeting circulating histones are lacking in current clinical practice. Extracorporeal blood purification, a widely used life support technique in intensive care units, is a promising therapeutic option for eliminating circulating histones. Inspired by electrostatic interactions between DNA chains and histones in natural nucleosomes, we propose a "one stone kills two birds" strategy to combat histone-related critical diseases by developing heparin-mimicking hydrogel microspheres (RCHMs). On one hand, the heparin-mimicking hydrogel structure inside RCHMs contains a large number of carboxyl and sulphonic acid groups by in situ cross-linking polymerization, which endows the RCHMs with excellent hemocompatibility. On the other hand, the RCHMs can adsorb circulating histones through electrostatic interactions. Our results demonstrate that the RCHMs do not cause significant hemolysis, blood cell activation and complement activation, with improved anti-protein contamination properties. The tailored RCHM microspheres (A3M1) can efficiently and selectively adsorb 91.16% of calf thymus histones with an adsorption capacity of 20.47 μg mg-1 within 4 h. Moreover, the RCHMs significantly attenuate histone-mediated thrombocytopenia, platelet aggregation, and endothelial cell death. Therefore, the RCHMs are promising hemoperfusion adsorbents for extracorporeal removal of circulating histones from the blood of critically ill patients, providing a new insight into the management of multiple histone-related disorders.

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来源期刊
Journal of materials chemistry. B
Journal of materials chemistry. B 化学科学, 工程与材料, 生命科学, 分析化学, 高分子组装与超分子结构, 高分子科学, 免疫生物学, 免疫学, 生化分析及生物传感, 组织工程学, 生物力学与组织工程学, 资源循环科学, 冶金与矿业, 生物医用高分子材料, 有机高分子材料, 金属材料的制备科学与跨学科应用基础, 金属材料, 样品前处理方法与技术, 有机分子功能材料化学, 有机化学
CiteScore
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