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用于缺血性血管再生的干细胞新型递送系统

New Delivery Systems of Stem Cells for Vascular Regeneration in Ischemia.

作者信息

Fakoya Adegbenro Omotuyi John

机构信息

Department of Anatomical Sciences, All Saints University School of Medicine , Roseau , Dominica.

出版信息

Front Cardiovasc Med. 2017 Feb 24;4:7. doi: 10.3389/fcvm.2017.00007. eCollection 2017.

Abstract

The finances of patients and countries are increasingly overwhelmed with the plague of cardiovascular diseases as a result of having to chronically manage the associated complications of ischemia such as heart failures, neurological deficits, chronic limb ulcers, gangrenes, and amputations. Hence, scientific research has sought for alternate therapies since pharmacological and surgical treatments have fallen below expectations in providing the desired quality of life. The advent of stem cells research has raised expectations with respect to vascular regeneration and tissue remodeling, hence assuring the patients of the possibility of an improved quality of life. However, these supposed encouraging results have been short-lived as the retention, survival, and engraftment rates of these cells appear to be inadequate; hence, the long-term beneficial effects of these cells cannot be ascertained. These drawbacks have led to the relentless research into better ways to deliver stem cells or angiogenic factors (which mobilize stem cells) to the regions of interest to facilitate increased retention, survival, engraftment, and regeneration. This review considered methods, such as the use of scaffolds, retrograde coronary delivery, improved combinations, stem cell pretreatment, preconditioning, stem cell exosomes, mannitol, magnet, and ultrasound-enhanced delivery, homing techniques, and stem cell modulation. Furthermore, the study appraised the possibility of a combination therapy of stem cells and macrophages, considering the enormous role macrophages play in repair, remodeling, and angiogenesis.

摘要

由于必须长期管理缺血相关并发症,如心力衰竭、神经功能缺损、慢性肢体溃疡、坏疽和截肢,患者和国家的财政日益不堪心血管疾病的重负。因此,由于药物和手术治疗在提供理想生活质量方面未达预期,科学研究一直在寻找替代疗法。干细胞研究的出现提高了人们对血管再生和组织重塑的期望,从而让患者确信生活质量有可能得到改善。然而,这些看似令人鼓舞的结果昙花一现,因为这些细胞的保留、存活和植入率似乎不足;因此,无法确定这些细胞的长期有益效果。这些缺点促使人们不断研究更好的方法,将干细胞或血管生成因子(可动员干细胞)输送到感兴趣的区域,以促进细胞的保留、存活、植入和再生增加。本综述探讨了多种方法,如使用支架、逆行冠状动脉输送、改进组合、干细胞预处理、预处理、干细胞外泌体、甘露醇、磁体和超声增强输送、归巢技术以及干细胞调节。此外,考虑到巨噬细胞在修复、重塑和血管生成中发挥的巨大作用,该研究评估了干细胞与巨噬细胞联合治疗的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4070/5323391/b1f50793c30a/fcvm-04-00007-g001.jpg

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