Department of Advanced Pathobiology, Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Izumisano, Japan.
Stem Cells Dev. 2013 Jul 15;22(14):2026-35. doi: 10.1089/scd.2012.0701. Epub 2013 Mar 15.
Thrombocytopenia (TTP) is a blood disease common to canines and human beings. Currently, there is no valid therapy for this disease except blood transfusion. In this study, we report the generation of canine induced pluripotent stem cells (ciPSCs) from canine embryonic fibroblasts, and a novel protocol for creating mature megakaryocytes (MKs) and functional platelets from ciPSCs. The ciPSCs were generated using lentiviral vectors, and differentiated into MKs and platelets on OP9 stromal cells supplemented with growth factors. Our ciPSCs presented in a tightly domed shape and showed expression of a critical pluripotency marker, REX1, and normal karyotype. Additionally, ciPSCs differentiated into cells derived from three germ layers via the formation of an embryoid body. The MKs derived from ciPSCs had hyperploidy and transformed into proplatelets. The proplatelets released platelets early on that expressed specific MK and platelet marker CD41/61. Interestingly, these platelets, when activated with adenosine diphosphate or thrombin, bind to fibrinogen. Moreover, electron microscopy showed that the platelets had the same ultrastructure as peripheral platelets. Thus, we have demonstrated for the first time the generation of ciPSCs that are capable of differentiating into MKs and release functional platelets in vitro. Our system for differentiating ciPSCs into MKs and platelets promises a critical therapy for canine TTP and appears to be extensible in principle to resolve human TTP.
血小板减少症(TTP)是犬类和人类常见的血液疾病。目前,除了输血之外,针对这种疾病还没有有效的治疗方法。在本研究中,我们报告了从犬胚胎成纤维细胞中生成犬诱导多能干细胞(ciPSCs)的情况,并介绍了一种从 ciPSCs 中生成成熟巨核细胞(MKs)和功能性血小板的新方案。ciPSCs 是通过慢病毒载体生成的,并在补充有生长因子的 OP9 基质细胞上分化为 MKs 和血小板。我们的 ciPSCs 呈现出紧密的穹顶形状,并表现出关键的多能性标志物 REX1 的表达和正常的核型。此外,ciPSCs 通过形成类胚体分化为来自三个胚层的细胞。从 ciPSCs 分化而来的 MKs 具有多倍体性,并转化为前血小板。这些前血小板早期释放出表达特定的 MK 和血小板标志物 CD41/61 的血小板。有趣的是,当这些血小板被二磷酸腺苷或凝血酶激活时,它们会与纤维蛋白原结合。此外,电子显微镜显示,这些血小板具有与外周血小板相同的超微结构。因此,我们首次证明了 ciPSCs 能够分化为 MKs 并在体外释放功能性血小板。我们的 ciPSCs 分化为 MKs 和血小板的系统有望为犬类 TTP 提供关键的治疗方法,并且原则上似乎可以扩展到解决人类 TTP。