Shiota Mitsutaka, Heike Toshio, Haruyama Munetada, Baba Shiro, Tsuchiya Atsunori, Fujino Hisanori, Kobayashi Hirohiko, Kato Takeo, Umeda Katsutsugu, Yoshimoto Momoko, Nakahata Tatsutoshi
Department of Pediatrics, Graduate School of Medicine, Kyoto University, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
Exp Cell Res. 2007 Mar 10;313(5):1008-23. doi: 10.1016/j.yexcr.2006.12.017. Epub 2007 Jan 8.
Sphere formation has been utilized as a way to isolate multipotent stem/progenitor cells from various tissues. However, very few studies on bone marrow-derived spheres have been published and assessed their multipotentiality. In this study, multipotent marrow cell populations were isolated using a three-step method. First, after elimination of hematopoietic cells, murine marrow-derived adherent cells were cultured in plastic dishes until small cells gradually appeared and multiplied. Cells were then cultured under non-adherent conditions and formed spheres that were immunopositive for a neural precursor marker, nestin. RT-PCR analysis also revealed that the spheres were positive for nestin in addition to PPARgamma, osf2, SOX9, and myoD, which are markers of precursors of adipocytic, osteoblastic, chondrocytic, and skeletal myeloblastic lineages, respectively. Finally, spheres were dissociated into single cells and expanded in adherent cultures. Under appropriate induction conditions, the sphere-derived cells acquired the phenotypic properties in vitro of neurons, skeletal myoblasts, and beating cardiomyocytes, as well as adipocytes, osteoblasts, and chondrocytes. Next, sphere-derived cells were transplanted into murine myocardial infarction models. One month later, they had become engrafted as cardiomyocytes, and cardiac catheterization showed significant functional improvements. Thus, sphere-derived cells represent a new approach to enhance the multi-differentiation potential of murine bone marrow.
球体形成已被用作从各种组织中分离多能干细胞/祖细胞的一种方法。然而,关于骨髓来源球体的研究很少发表,也没有评估它们的多能性。在本研究中,使用三步法分离多能骨髓细胞群体。首先,在消除造血细胞后,将小鼠骨髓来源的贴壁细胞在塑料培养皿中培养,直到小细胞逐渐出现并增殖。然后将细胞在非贴壁条件下培养,形成对神经前体标志物巢蛋白呈免疫阳性的球体。RT-PCR分析还显示,除了分别作为脂肪细胞、成骨细胞、软骨细胞和骨骼肌成髓细胞系前体标志物的PPARγ、osf2、SOX9和肌分化抗原(MyoD)外,球体对巢蛋白也呈阳性。最后,将球体解离为单细胞并在贴壁培养中扩增。在适当的诱导条件下,球体来源的细胞在体外获得了神经元、骨骼肌成肌细胞和跳动心肌细胞以及脂肪细胞、成骨细胞和软骨细胞的表型特性。接下来,将球体来源的细胞移植到小鼠心肌梗死模型中。一个月后,它们已作为心肌细胞植入,心脏导管检查显示功能有显著改善。因此,球体来源的细胞代表了一种增强小鼠骨髓多分化潜能的新方法。