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CXCR7表达增强促进内皮祖细胞血管生成能力
  • 时间:0
  • 分类:R96[医药卫生—药理学;医药卫生—药学]
  • 作者机构:温州医科大学药学院中美糖尿病并发症研究所,浙江温州325035
  • 相关基金:温州市公益性科技计划项目(Y2014-0654);国家自然科学基金青年基金资助项目(81200239).
中文摘要:

目的:考察提高CXCR7表达能否提高内皮祖细胞(EPCs)血管生成能力。方法:利用高表达CXCR7的腺病毒转染至人脐带血来源的EPCs,建立CXCR7high-EPCs工程化细胞。比较CXCR7high-EPCs与对照组EPCs在无血清条件下存活、黏附、经基质细胞衍生因子-1(SDF-1)诱导的跨内皮迁移、管样结构形成以及一氧化氮(NO)生成能力。结果:高表达CXCR7能显著增强EPCs在无血清条件下细胞存活能力、黏附功能、SDF-1诱导的跨内皮迁移、管样结构形成以及EPCs生成NO的能力,并且与SDF-1有协同作用。结论:提高CXCR7在人脐带血来源的EPCs中表达能够增强其血管生成能力,这为临床治疗血管性疾病提供新思路。

英文摘要:

Objective: To investigate whether increasing CXCR7 expression in endothelial progenitor cells (EPCs) can improve its angiogenic capability. Methods: CXCR7M~H-EPCs were constructed by transfecting with adenovirus carring human CXCR7 gene. The differences between CXCR7high-EPCs and wt-EPC in cell survival under serum deprivation condition, adhesion, SDF-1 induced trans-endothelial migration, tube formation and ni- tric oxide (NO) production were compared. Results: Compared with ctrl-EPCs, CXCR7high-EPCs has superiority in cell survival under serum-free condition, cell adhension to activated endothelial cells, trans-endothelial migra- tion, tube formation and NO production, which could be further enhanced by SDF-1. Conclusion: Increasing expression of CXCR7 can enhance the angiogenic capacity of EPCs. The performance of present research may provide a new idea for the treatment of vascular diseases.

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