Rosová Ivana, Dao Mo, Capoccia Ben, Link Daniel, Nolta Jan A
Stem Cell Program, University of California at Davis, Room 653, 2425 Stockton Boulevard, Sacramento, California 95817, USA.
Stem Cells. 2008 Aug;26(8):2173-82. doi: 10.1634/stemcells.2007-1104. Epub 2008 May 29.
Mesenchymal stem cells (MSC) are adult multipotent cells found in bone marrow, adipose tissue, and other adult tissues. MSC have been shown to improve regeneration of injured tissues in vivo, but the mechanisms remain unclear. Typically, MSC are cultured under ambient, or normoxic, conditions (21% oxygen). However, the physiological niches for MSC in the bone marrow and other sites have much lower oxygen tension. When used as a therapeutic tool to repair tissue injuries, MSC cultured in standard conditions must adapt from 21% oxygen in culture to less than 1% oxygen in the ischemic tissue. We therefore examined the effects of preculturing human bone marrow-derived MSC in hypoxic conditions (1%-3% oxygen) to elucidate the best conditions that enhance their tissue regenerative potential. We demonstrated that MSC cultured in hypoxia activate the Akt signaling pathway while maintaining their viability and cell cycle rates. We also showed that MSC cultured in hypoxia induced expression of cMet, the major receptor for hepatocyte growth factor (HGF), and enhanced cMet signaling. MSC cultured in hypoxic conditions increased their migration rates. Since migration and HGF responsiveness are thought to be key mediators of MSC recruitment and/or activation in vivo, we next examined the tissue regenerative potential of MSC cultured under hypoxic conditions, using a murine hind limb ischemia model. We showed that local expression of HGF is increased in ischemic muscle in this model. Intra-arterial injection of MSC cultured in either normoxic or hypoxic conditions 24 hours after surgical induction of hind limb ischemia enhanced revascularization compared with saline controls. However, restoration of blood flow was observed significantly earlier in mice that had been injected with hypoxic preconditioned MSC. Collectively, these data suggest that preculturing MSC under hypoxic conditions prior to transplantation improves their tissue regenerative potential. Disclosure of potential conflicts of interest is found at the end of this article.
间充质干细胞(MSC)是存在于骨髓、脂肪组织和其他成人组织中的成体多能细胞。已有研究表明,MSC可在体内促进受损组织的再生,但其机制仍不清楚。通常情况下,MSC在环境氧或常氧条件(21%氧气)下培养。然而,骨髓和其他部位的MSC生理微环境的氧张力要低得多。当用作修复组织损伤的治疗工具时,在标准条件下培养的MSC必须从培养环境中的21%氧气适应到缺血组织中低于1%的氧气环境。因此,我们研究了在低氧条件(1%-3%氧气)下预培养人骨髓来源的MSC的效果,以阐明增强其组织再生潜力的最佳条件。我们证明,在低氧条件下培养的MSC在维持其活力和细胞周期速率的同时激活了Akt信号通路。我们还表明,在低氧条件下培养的MSC诱导了肝细胞生长因子(HGF)的主要受体cMet的表达,并增强了cMet信号传导。在低氧条件下培养的MSC提高了其迁移速率。由于迁移和对HGF的反应性被认为是体内MSC募集和/或激活的关键介质,接下来我们使用小鼠后肢缺血模型研究了在低氧条件下培养的MSC的组织再生潜力。我们发现,在该模型中缺血肌肉中HGF的局部表达增加。在手术诱导后肢缺血24小时后,经动脉注射在常氧或低氧条件下培养的MSC,与生理盐水对照组相比,增强了血管再生。然而,在注射了低氧预处理MSC的小鼠中,血流恢复明显更早。总体而言,这些数据表明,在移植前在低氧条件下预培养MSC可提高其组织再生潜力。潜在利益冲突的披露见本文末尾。