A preventive injection of endothelial progenitor cells prolongs lifespan in stroke-prone spontaneously hypertensive rats

Author:

Peng Cheng1,Dong Xiao-Hui2,Liu Jia-Lin1,Tao Yu-Long3,Xu Chun-Fang4,Wang Li-Ping1,Liu Chun-Long1,Su Ding-Feng4,Tao Xia3,Zhang Chuan4,Chen Alex F.56,Xie He-Hui145

Affiliation:

1. School of Public Health and Hongqiao International Institute of Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

2. Department of Pharmacy, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China

3. Department of Pharmacy, Shanghai Changzheng Hospital, The Second Military Medical University, Shanghai 200120, China

4. Department of Identification of Traditional Chinese Medicine and Department of Pharmacology, The Second Military Medical University, Shanghai 200433, China

5. Third Xiangya Hospital and the Institute of Vascular Disease and Translational Medicine, Central South University, Changsha, Hunan 410013, China

6. Institute of Development and Regenerative Medicine, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092

Abstract

There is a pressing need for new approaches to prevent stroke. Endothelial progenitor cells (EPCs) promote vascular repair and revascularization in the ischemic brain. The present study sought to evaluate whether preventive delivery of EPCs could prevent or protect against stroke. Stroke-prone spontaneously hypertensive rats (SHR-SP) received a single injection of EPCs, and their survival time was monitored. In addition, at 28 and/or 42 days after a single injection of EPCs, SHR-SP and mice were subjected to cerebral ischemia, and cerebral ischemic injury, local angiogenesis and in vivo EPC integration were determined. Other experiments examined the effects of EPC conditioned medium, and the distribution of donor EPCs taken from GFP transgenic mice. It was found that EPC-pretreated SHR-SP showed longer lifespans than untreated controls. A single preventive injection of EPCs could produce persistent protective effects against cerebral ischemic injury (lasting at least 42 days), and promote local angiogenesis in the ischemic brain, in two types of animals (SHR-SP and normotensive mice). EPCs of donor origin could be detected in the recipient peripheral blood, and integrated into the recipient ischemic brains. Furthermore, it was suggested that mouse EPCs might exert paracrine effects on cerebral ischemic injury in addition to their direct angiogenic effects. In conclusion, a single preventive injection of EPCs prolonged the lifespan of SHR-SP, and protected against cerebral ischemic injury for at least 7 weeks. It is implied that EPC injection might be a promising candidate for a preventive role in patients at high risk for stroke.

Publisher

Portland Press Ltd.

Subject

General Medicine

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