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抗坏血酸促进胚胎干细胞向破骨细胞分化。

Ascorbic acid promotes osteoclastogenesis from embryonic stem cells.

作者信息

Tsuneto Motokazu, Yamazaki Hidetoshi, Yoshino Miya, Yamada Takayuki, Hayashi Shin-Ichi

机构信息

Division of Immunology, Department of Molecular and Cellular Biology, School of Life Science, Faculty of Medicine, Tottori University, Yonago, Tottori 683-8503, Japan.

出版信息

Biochem Biophys Res Commun. 2005 Oct 7;335(4):1239-46. doi: 10.1016/j.bbrc.2005.08.016.

DOI:10.1016/j.bbrc.2005.08.016
PMID:16112648
Abstract

Ascorbic acid (AA) is known to regulate cell differentiation; however, the effects of AA on osteoclastogenesis, especially on its early stages, remain unclear. To examine the effects of AA throughout the process of osteoclast development, we established a culture system in which tartrate-resistant acid phosphate (TRAP)-positive osteoclasts were induced from embryonic stem cells without stromal cell lines. In this culture system, the number of TRAP-positive cells was strongly increased by the addition of AA during the development of osteoclast precursors, and reducing agents, 2-mercaptoethanol, monothioglycerol, and dithiothreitol, failed to substitute for AA. The effect of AA was stronger when it was added during the initial 4 days during the development of mesodermal cells than when it was added during the last 4 days. On day 4 of the culture period, AA increased the total cell recovery and frequency of osteoclast precursors. Magnetic cell sorting using anti-Flk-1 antibody enriched osteoclast precursors on day 4, and the proportion of Flk-1-positive cells but not that of platelet-derived growth factor receptor alpha-positive cells was increased by the addition of AA. These results suggest that AA might promote osteoclastogenesis of ES cells through increasing Flk-1-positive cells, which then give rise to osteoclast precursors.

摘要

已知抗坏血酸(AA)可调节细胞分化;然而,AA对破骨细胞生成的影响,尤其是对其早期阶段的影响仍不清楚。为了研究AA在破骨细胞发育全过程中的作用,我们建立了一种培养体系,在无基质细胞系的情况下,从胚胎干细胞诱导生成抗酒石酸酸性磷酸酶(TRAP)阳性的破骨细胞。在该培养体系中,在破骨细胞前体发育过程中添加AA可显著增加TRAP阳性细胞的数量,而还原剂2-巯基乙醇、单硫甘油和二硫苏糖醇无法替代AA。在中胚层细胞发育的最初4天添加AA时的效果比在最后4天添加时更强。在培养期第4天,AA增加了细胞总回收率和破骨细胞前体的频率。使用抗Flk-1抗体进行磁性细胞分选在第4天富集了破骨细胞前体,添加AA可增加Flk-1阳性细胞的比例,但不会增加血小板衍生生长因子受体α阳性细胞的比例。这些结果表明,AA可能通过增加Flk-1阳性细胞来促进ES细胞的破骨细胞生成,而这些Flk-1阳性细胞随后会产生破骨细胞前体。

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