首页> 外文学位 >Adult Bone Marrow Mesenchymal Stem Cells Primed for fhe Repair of Damaged Cardiac Tissue After Myocardial Infarction.
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Adult Bone Marrow Mesenchymal Stem Cells Primed for fhe Repair of Damaged Cardiac Tissue After Myocardial Infarction.

机译:灌注成年骨髓间充质干细胞,用于心肌梗塞后受损心脏组织的修复。

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摘要

The burden of cardiovascular disease around the world is growing, despite improvements in hospital care and time to treatment. As more people survive an initial myocardial infarction (MI), the decompensated heart tissue is strained, leading to heart failure (HF) and an increased risk for a second MI. While extensive progress has been made in treating the symptoms after MI, including HF and angina, little success has come from repairing the damaged heart tissue to alleviate the progression to these end- stage symptoms. One promising area of regenerative research has been the use of adult stem cells, particularly from the bone marrow (BMSCs). These cells can differentiate towards the cardiac cell lineage in vitro while producing trophic factors that can repair damaged tissue. When placed in the heart after MI though, BMSCs have mixed results, producing profound changes in some patients but zero or even negative effects in others. In this report, we used BMSCs as a stem cell base for a regenerative medicine system for the repair of damaged cardiac tissue. These cells are seeded on a polycaprolactone nanoscaffolding support system, which provides a growth substrate for in vitro work, as well as a housing system for protected in vivo delivery. When the nanoscaffold is pre-coated with a novel combination of a cardiac protein, thymosin beta4 (Tbeta4), and a small molecule effector of the WNT protein pathway, IWP-2, BMSCs differentiated towards the cardiac lineage in as little as 24hours. When injected into rat hearts that have been given an ischemic MI, the nanoscaffolding system slowly dissolves, leaving the cells in place of the damaged cardiac tissue. After two weeks of monitoring, BMSCs are present within the damaged hearts, as evidenced by immunofluorescence and nanoparticle tracking. Injections of the nanoscaffolding/cell system led to robust healing of the rat hearts that had been given small- and medium- damage heart attacks, outperforming PBS sham and cell culture media injections. Significant improvements in cardiac metrics, including ejection fraction and left ventricular end systolic volume, were seen compared to untreated animals, and were comparable to healthy controls. To our knowledge this is the first side-by-side comparison of cell culture media and stem cells to heal a predefined range of MI damage. We believe this simple, inexpensive treatment option is a new beneficial step towards healing damaged patient tissue after MI.
机译:尽管改善了医院护理并缩短了治疗时间,但全世界心血管疾病的负担仍在增加。随着越来越多的人在最初的心肌梗死(MI)中幸存下来,失代偿的心脏组织会拉紧,导致心力衰竭(HF),并增加第二次MI的风险。尽管在治疗心力衰竭后的症状(包括心力衰竭和心绞痛)方面已取得了广泛的进展,但修复受损的心脏组织以减轻其发展为这些终末期症状的进展甚微。再生研究的一个有希望的领域是成人干细胞的使用,特别是来自骨髓(BMSCs)的干细胞。这些细胞可以在体外分化为心肌细胞谱系,同时产生可以修复受损组织的营养因子。然而,当放置在MI后的心脏中时,BMSC的结果好坏参半,在某些患者中产生了深远的变化,而在其他患者中则产生了零甚至负面影响。在本报告中,我们将BMSCs用作再生医学系统的干细胞基础,以修复受损的心脏组织。这些细胞被接种到聚己内酯纳米支架支持系统上,该系统为体外工作提供了生长基质,并为保护体内递送提供了住房系统。当纳米支架预涂有心脏蛋白,胸腺素β4(Tbeta4)和WNT蛋白途径的小分子效应子IWP-2的新型组合时,BMSC会在短短24小时内向心脏谱系分化。将纳米支架注射到已经缺血的MI大鼠心脏中后,它会缓慢溶解,从而使细胞代替受损的心脏组织。监测两周后,受损的心脏内存在BMSC,免疫荧光和纳米颗粒追踪证明了这一点。纳米支架/细胞系统的注射可导致老鼠心脏得到强健的愈合,而老鼠心脏受到中度和中度的破坏,表现优于PBS假手术和细胞培养基注射。与未经治疗的动物相比,可以看到心脏指标(包括射血分数和左心室收缩末期容积)的显着改善,与健康对照组相当。据我们所知,这是细胞培养基和干细胞治愈预定范围的MI损伤的首次并排比较。我们认为,这种简单,廉价的治疗选择是治愈MI后受损患者组织的新的有益步骤。

著录项

  • 作者

    Marks, Edward D.;

  • 作者单位

    University of Delaware.;

  • 授予单位 University of Delaware.;
  • 学科 Nanoscience.;Cellular biology.
  • 学位 Ph.D.
  • 年度 2017
  • 页码 164 p.
  • 总页数 164
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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