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基于间充质干细胞的心血管疾病治疗:进展与挑战。

Mesenchymal Stem Cell-Based Therapy for Cardiovascular Disease: Progress and Challenges.

机构信息

Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA; Department of Cell Biology and Biophysics, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

出版信息

Mol Ther. 2018 Jul 5;26(7):1610-1623. doi: 10.1016/j.ymthe.2018.05.009. Epub 2018 May 25.

Abstract

Administration of mesenchymal stem cells (MSCs) to diseased hearts improves cardiac function and reduces scar size. These effects occur via the stimulation of endogenous repair mechanisms, including regulation of immune responses, tissue perfusion, inhibition of fibrosis, and proliferation of resident cardiac cells, although rare events of transdifferentiation into cardiomyocytes and vascular components are also described in animal models. While these improvements demonstrate the potential of stem cell therapy, the goal of full cardiac recovery has yet to be realized in either preclinical or clinical studies. To reach this goal, novel cell-based therapeutic approaches are needed. Ongoing studies include cell combinations, incorporation of MSCs into biomaterials, or pre-conditioning or genetic manipulation of MSCs to boost their release of paracrine factors, such as exosomes, growth factors, microRNAs, etc. All of these approaches can augment therapeutic efficacy. Further study of the optimal route of administration, the correct dose, the best cell population(s), and timing for treatment are parameters that still need to be addressed in order to achieve the goal of complete cardiac regeneration. Despite significant progress, many challenges remain.

摘要

将间充质干细胞(MSCs)施用于患病心脏可改善心脏功能并减少疤痕面积。这些作用是通过刺激内源性修复机制实现的,包括调节免疫反应、组织灌注、抑制纤维化和促进驻留的心肌细胞增殖,尽管在动物模型中也描述了罕见的转分化为心肌细胞和血管成分的事件。尽管这些改善表明了干细胞治疗的潜力,但在临床前或临床研究中尚未实现完全的心脏恢复目标。为了实现这一目标,需要新的基于细胞的治疗方法。正在进行的研究包括细胞组合、将 MSC 纳入生物材料中、或对 MSC 进行预处理或遗传操作以增强其旁分泌因子(如外泌体、生长因子、microRNAs 等)的释放。所有这些方法都可以增强治疗效果。为了实现完全心脏再生的目标,仍需要进一步研究最佳给药途径、正确剂量、最佳细胞群和治疗时机等参数。尽管取得了重大进展,但仍存在许多挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/851b/6037203/ef04ddd10f62/fx1.jpg

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