Rufaihah Abdul Jalil, Yasa I Ceren, Ramanujam Vaibavi Srirangam, Arularasu Suganya Cheyyatraivendran, Kofidis Theo, Guler Mustafa O, Tekinay Ayse B
Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Institute of Materials Science and Nanotechnology, National Nanotechnology Research Center (UNAM), Bilkent University, Ankara 06800, Turkey.
Acta Biomater. 2017 Aug;58:102-112. doi: 10.1016/j.actbio.2017.06.009. Epub 2017 Jun 13.
Myocardial infarction remains one of the top leading causes of death in the world and the damage sustained in the heart eventually develops into heart failure. Limited conventional treatment options due to the inability of the myocardium to regenerate after injury and shortage of organ donors require the development of alternative therapies to repair the damaged myocardium. Current efforts in repairing damage after myocardial infarction concentrates on using biologically derived molecules such as growth factors or stem cells, which carry risks of serious side effects including the formation of teratomas. Here, we demonstrate that synthetic glycosaminoglycan (GAG) mimetic peptide nanofiber scaffolds induce neovascularization in cardiovascular tissue after myocardial infarction, without the addition of any biologically derived factors or stem cells. When the GAG mimetic nanofiber gels were injected in the infarct site of rodent myocardial infarct model, increased VEGF-A expression and recruitment of vascular cells was observed. This was accompanied with significant degree of neovascularization and better cardiac performance when compared to the control saline group. The results demonstrate the potential of future clinical applications of these bioactive peptide nanofibers as a promising strategy for cardiovascular repair.
We present a synthetic bioactive peptide nanofiber system can enhance cardiac function and enhance cardiovascular regeneration after myocardial infarction (MI) without the addition of growth factors, stem cells or other biologically derived molecules. Current state of the art in cardiac repair after MI utilize at least one of the above mentioned biologically derived molecules, thus our approach is ground-breaking for cardiovascular therapy after MI. In this work, we showed that synthetic glycosaminoglycan (GAG) mimetic peptide nanofiber scaffolds induce neovascularization and cardiomyocyte differentiation for the regeneration of cardiovascular tissue after myocardial infarction in a rat infarct model. When the peptide nanofiber gels were injected in infarct site at rodent myocardial infarct model, recruitment of vascular cells was observed, neovascularization was significantly induced and cardiac performance was improved. These results demonstrate the potential of future clinical applications of these bioactive peptide nanofibers as a promising strategy for cardiovascular repair.
心肌梗死仍然是全球主要死因之一,心脏遭受的损伤最终会发展为心力衰竭。由于心肌损伤后无法再生以及器官供体短缺,传统治疗选择有限,因此需要开发替代疗法来修复受损心肌。目前修复心肌梗死后损伤的努力主要集中在使用生物衍生分子,如生长因子或干细胞,但这些方法存在严重副作用的风险,包括畸胎瘤的形成。在此,我们证明合成糖胺聚糖(GAG)模拟肽纳米纤维支架可在心肌梗死后诱导心血管组织新生血管形成,而无需添加任何生物衍生因子或干细胞。当将GAG模拟纳米纤维凝胶注射到啮齿动物心肌梗死模型的梗死部位时,观察到血管内皮生长因子A(VEGF-A)表达增加和血管细胞募集。与对照盐水组相比,这伴随着显著程度的新生血管形成和更好的心脏功能。结果表明,这些生物活性肽纳米纤维未来具有临床应用潜力,是心血管修复的一种有前景的策略。
我们提出一种合成生物活性肽纳米纤维系统,可在不添加生长因子、干细胞或其他生物衍生分子的情况下增强心肌梗死后的心脏功能并促进心血管再生。目前心肌梗死后心脏修复的现有技术至少使用上述生物衍生分子中的一种,因此我们的方法在心肌梗死后的心血管治疗方面具有开创性。在这项工作中,我们表明合成糖胺聚糖(GAG)模拟肽纳米纤维支架在大鼠梗死模型中可诱导心肌梗死后心血管组织再生的新生血管形成和心肌细胞分化。当将肽纳米纤维凝胶注射到啮齿动物心肌梗死模型的梗死部位时,观察到血管细胞募集,显著诱导了新生血管形成并改善了心脏功能。这些结果表明,这些生物活性肽纳米纤维未来具有临床应用潜力,是心血管修复的一种有前景的策略。