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The anti-microbial peptide SR-0379 stimulates human endothelial progenitor cell-mediated repair of peripheral artery diseases

机译:抗菌肽SR-0379刺激人内皮祖细胞介导的外周动脉疾病修复

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摘要

Ischemia is a serious disease, characterized by an inadequate blood supply to an organ or part of the body. In the present study, we evaluated the effects of the anti-microbial peptide SR-0379 on the stem cell-mediated therapy of ischemic diseases. The migratory and tube-forming abilities of human endothelial progenitor cells (EPCs) were enhanced by treatment with SR-0379 in vitro. Intramuscular administration of SR-0379 into a murine ischemic hindlimb significantly enhanced blood perfusion, decreased tissue necrosis, and increased the number of blood vessels in the ischemic muscle. Moreover, co-administration of SR-0379 with EPCs stimulated blood perfusion in an ischemic hindlimb more than intramuscular injection with either SR-0379 or EPCs alone. This enhanced blood perfusion was accompanied by a significant increase in the number of CD31- and α-SMA-positive blood vessels in ischemic hindlimb. These results suggest that SR-0379 is a potential drug candidate for potentiating EPC-mediated therapy of ischemic diseases.
机译:缺血是一种严重的疾病,其特征是器官或身体局部血液供应不足。在本研究中,我们评估了抗微生物肽SR-0379在干细胞介导的缺血性疾病治疗中的作用。体外用SR-0379处理可增强人内皮祖细胞(EPC)的迁移和成管能力。将SR-0379肌肉内给药至鼠类缺血性后肢可显着增强血液灌注,减少组织坏死并增加缺血性肌肉中的血管数量。此外,与单独使用SR-0379或单独使用EPC的肌肉注射相比,将SR-0379与EPC共同使用刺激的缺血后肢血液灌注更强。这种血液灌注的增加伴随着缺血性后肢中CD31和α-SMA阳性血管数量的显着增加。这些结果表明,SR-0379是增强EPC介导的缺血性疾病治疗的潜在候选药物。

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