Wang Meijing, Tan Jiangning, Coffey Arthur, Fehrenbacher John, Weil Brent R, Meldrum Daniel R
Department of Surgery, Indiana University School of Medicine, Indianapolis, Ind, USA.
J Thorac Cardiovasc Surg. 2009 Jul;138(1):163-71, 171.e1. doi: 10.1016/j.jtcvs.2009.03.010.
Vascular endothelial growth factor, a critical factor in angiogenesis, mediates stem cell paracrine protective effects on ischemic myocardium. Studies on the role of sex in stem cell function have demonstrated that female mesenchymal stem cells produce greater vascular endothelial growth factor and provide better cardiac protection compared with male mesenchymal stem cells. The purpose of this study was to determine the mechanisms by which estrogen affects mesenchymal stem cell function as a potential therapeutic measure during ex vivo expansion, before therapeutic use.
A single-step purification method using adhesion to cell culture plastic was adopted to isolate mesenchymal stem cells from wild-type, estrogen receptor-alpha knockout, estrogen receptor-beta knockout, and signal transducer and activator of transcription 3 knockout mice. Mesenchymal stem cells were treated with or without 17beta-estradiol, estrogen receptor-alpha agonist (propyl pyrazoletriol), and estrogen receptor-beta agonist (diarylpropionitrile).
17beta-estradiol significantly increased mesenchymal stem cell vascular endothelial growth factor production in a dose-dependent manner. Both estrogen receptor-alpha and estrogen receptor-beta were expressed in mesenchymal stem cells. Administration of 17beta-estradiol or estrogen receptor-alpha agonist (not estrogen receptor-beta agonist) elevated mesenchymal stem cell vascular endothelial growth factor, hypoxia inducible factor-1alpha expression, and signal transducer and activator of transcription 3 activation. However, these effects were neutralized in estrogen receptor-alpha knockout mesenchymal stem cells, not estrogen receptor-beta knockout. Signal transducer and activator of transcription 3 knockout abolished estrogen receptor-alpha-induced hypoxia inducible factor-1alpha and subsequent vascular endothelial growth factor production.
17beta-estradiol-induced vascular endothelial growth factor production from mesenchymal stem cells appears to be mediated through estrogen receptor-alpha-activated signal transducer and activator of transcription 3-mediated hypoxia inducible factor-1alpha expression.
血管内皮生长因子是血管生成中的关键因子,介导干细胞对缺血心肌的旁分泌保护作用。关于性别在干细胞功能中作用的研究表明,与雄性间充质干细胞相比,雌性间充质干细胞产生更多的血管内皮生长因子,并能提供更好的心脏保护作用。本研究的目的是确定雌激素在体外扩增期间影响间充质干细胞功能的机制,以便在治疗前进行潜在的治疗措施研究。
采用细胞培养塑料贴壁的单步纯化方法,从野生型、雌激素受体α敲除、雌激素受体β敲除以及信号转导和转录激活因子3敲除小鼠中分离间充质干细胞。间充质干细胞分别用或不用17β-雌二醇、雌激素受体α激动剂(丙基吡唑三醇)和雌激素受体β激动剂(二芳基丙腈)处理。
17β-雌二醇以剂量依赖性方式显著增加间充质干细胞血管内皮生长因子的产生。雌激素受体α和雌激素受体β均在间充质干细胞中表达。给予17β-雌二醇或雌激素受体α激动剂(而非雌激素受体β激动剂)可提高间充质干细胞血管内皮生长因子、缺氧诱导因子-1α的表达以及信号转导和转录激活因子3的激活。然而,这些作用在雌激素受体α敲除的间充质干细胞中被中和,而在雌激素受体β敲除的细胞中未被中和。信号转导和转录激活因子3敲除消除了雌激素受体α诱导的缺氧诱导因子-1α以及随后血管内皮生长因子的产生。
17β-雌二醇诱导间充质干细胞产生血管内皮生长因子似乎是通过雌激素受体α激活的信号转导和转录激活因子3介导的缺氧诱导因子-1α表达来实现的。