Bussche Leen, Van de Walle Gerlinde R
Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA
Stem Cells Transl Med. 2014 Dec;3(12):1514-25. doi: 10.5966/sctm.2014-0138. Epub 2014 Oct 13.
Mesenchymal stromal cells (MSCs) have received much attention as a potential treatment of ischemic diseases, including ischemic tissue injury and cardiac failure. The beneficial effects of MSCs are thought to be mediated by their ability to provide proangiogenic factors, creating a favorable microenvironment that results in neovascularization and tissue regeneration. To study this in more detail and to explore the potential of the horse as a valuable translational model, the objectives of the present study were to examine the presence of angiogenic stimulating factors in the conditioned medium (CM) of peripheral blood-derived equine mesenchymal stromal cells (PB-MSCs) and to study their in vitro effect on angiogenesis-related endothelial cell (EC) behavior, including proliferation and vessel formation. Our salient findings were that CM from PB-MSCs contained significant levels of several proangiogenic factors. Furthermore, we found that CM could induce angiogenesis in equine vascular ECs and confirmed that endothelin-1, insulin growth factor binding protein 2, interleukin-8, and platelet-derived growth factor-AA, but not urokinase-type plasminogen activator, were responsible for this enhanced EC network formation by increasing the expression level of vascular endothelial growth factor-A, an important angiogenesis stimulator.
间充质基质细胞(MSCs)作为缺血性疾病(包括缺血性组织损伤和心力衰竭)的一种潜在治疗方法受到了广泛关注。MSCs的有益作用被认为是通过其提供促血管生成因子的能力来介导的,从而创造一个有利于新血管形成和组织再生的微环境。为了更详细地研究这一点,并探索马作为一种有价值的转化模型的潜力,本研究的目的是检测外周血来源的马间充质基质细胞(PB-MSCs)条件培养基(CM)中血管生成刺激因子的存在,并研究它们对血管生成相关内皮细胞(EC)行为(包括增殖和血管形成)的体外影响。我们的显著发现是,PB-MSCs的CM中含有大量几种促血管生成因子。此外,我们发现CM可以诱导马血管内皮细胞的血管生成,并证实内皮素-1、胰岛素生长因子结合蛋白2、白细胞介素-8和血小板衍生生长因子-AA,但不是尿激酶型纤溶酶原激活剂,通过增加重要的血管生成刺激因子血管内皮生长因子-A的表达水平,导致这种增强的内皮细胞网络形成。