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载丹参素酸 B 和 L-抗坏血酸 2-磷酸镁的心脏模拟核壳纳米纤维支架的心肌细胞分化的策略设计。

Strategic design of cardiac mimetic core-shell nanofibrous scaffold impregnated with Salvianolic acid B and Magnesium l-ascorbic acid 2 phosphate for myoblast differentiation.

机构信息

Biological Materials Laboratory, CSIR - Central Leather Research Institute, Adyar, Chennai, 600020, Tamil Nadu, India.

Biological Materials Laboratory, CSIR - Central Leather Research Institute, Adyar, Chennai, 600020, Tamil Nadu, India.

出版信息

Mater Sci Eng C Mater Biol Appl. 2018 Sep 1;90:131-147. doi: 10.1016/j.msec.2018.04.056. Epub 2018 Apr 21.

Abstract

The major loss of myocardial tissue extracellular matrix after infarction is a serious complication that leads to heart failure. Regeneration and integration of damaged cardiac tissue is challenging since the functional restoration of the injured myocardium is an incredible task. The injured micro environment of myocardium fails to regenerate spontaneously. The emergence of nano-biomaterials would be a promising approach to regenerate such a damaged cardiomyocytes tissue. Here, we have fabricated a dual bioactive embedded nanofibrous cardiac patch via coaxial electrospinning technique, to mimic the topographical and chemical cues of the natural cardiac tissue. The proportion and the concentration of the polymers were optimized for tailored delivery of bioactives from a spatio-temporally designed scaffold. The functionalization of polymeric core shell nanofibrous scaffold with dual bioactives enhanced the physico-chemical and bio-mechanical properties of the scaffolds that has resulted in a 3-dimensional topography mimicking the natural cardiac like extracellular matrix. The sustained delivery of bioactive signals, improved cell adhesion, proliferation, migration and differentiation could be attributed to its highly interconnected nanofibrous matrix with good extended morphology. Further, the expression of cardiac specific markers were found to increase on investigation of mRNA by real time PCR studies and proteins by immunofluorescence and western blotting techniques, confirming cell - biomaterial interactions. Flow cytometry analysis authenticated a potent mitochondrial membrane potential of cells treated with nanocomposite. In addition, in ovo studies in chicken chorioallantoic membrane assay confirm the efficacy of the developed scaffold in inducing angiogenesis required for maintaining its viability after transplantation onto the infarcted zone. These promising results demonstrate the potential of the composite nanofibrous scaffold as an effective biomaterial substrate for cardiac regeneration providing cues for development of novel cardiac therapeutics.

摘要

梗死后心肌组织细胞外基质的主要损失是导致心力衰竭的严重并发症。由于损伤心肌的功能恢复是一项艰巨的任务,因此受损的心脏组织的再生和整合具有挑战性。受伤的心肌微环境无法自发再生。纳米生物材料的出现将是一种有前途的方法,可以再生受损的心肌细胞组织。在这里,我们通过同轴静电纺丝技术制造了一种双生物活性嵌入式纳米纤维心脏补片,以模拟天然心脏组织的形貌和化学线索。通过时空设计支架,优化了聚合物的比例和浓度,以定制生物活性物质的传递。聚合物核壳纳米纤维支架的双生物活性功能化增强了支架的物理化学和生物力学性能,使其具有模仿天然心脏样细胞外基质的 3 维形貌。生物活性信号的持续释放、改善的细胞黏附、增殖、迁移和分化可归因于其具有良好的延伸形态的高度互联纳米纤维基质。此外,通过实时 PCR 研究和免疫荧光及 Western blot 技术研究蛋白质,发现心脏特异性标志物的表达增加,证实了细胞-生物材料相互作用。流式细胞术分析证实了用纳米复合材料处理的细胞具有强大的线粒体膜电位。此外,鸡胚绒毛尿囊膜试验中的体内研究证实了所开发的支架在诱导血管生成方面的功效,这对于在移植到梗死区后维持其活力是必需的。这些有希望的结果表明,复合纳米纤维支架作为有效的心脏再生生物材料基质具有潜力,为开发新型心脏治疗方法提供了线索。

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