Boban Ivana, Barisic-Dujmovic Tatjana, Clark Stephen H
Department of Genetics and Developmental Biology, University of Connecticut Stem Cell Institute, University of Connecticut Health Center, Farmington, Connecticut 06030, USA.
Genesis. 2010 Mar;48(3):171-82. doi: 10.1002/dvg.20602.
The goal of this study was to determine the presence of osteoprogenitor cells in the peripheral blood. Experiments were conducted with a parabiosis model in which osteoblast specific transgenic mice (Col2.3GFP or hOC-GFP) were surgically joined with a transgenic mouse where herpes virus thymidine kinase gene is under the control of the collagen alpha1 promoter (Col2.3DeltaTK). This method permits conditional ablation of osteoblasts by ganciclovir (GCV) treatment. In parabionts treated with GCV for 15 days or 1.5-2 months, GFP (hOC-GFP or Col2.3GFP) expression was not detected in histological preparations or in marrow stromal cell cultures from the Col2.3DeltaTK parabiont. Finally, Col2.3GFP/Col2.3DeltaTK pairs were treated with GCV for 15 days and allowed to recover from GCV for 3 months. Again there was a failure to detect Col2.3GFP expressing cells in the Col2.3DeltaTK parabiont. These observations, at least within the limits of this model system, allow the conclusion that osteoprogenitor cells do not readily circulate.
本研究的目的是确定外周血中是否存在骨祖细胞。实验采用联体共生模型,将成骨细胞特异性转基因小鼠(Col2.3GFP或hOC-GFP)与疱疹病毒胸苷激酶基因受胶原蛋白α1启动子(Col2.3DeltaTK)控制的转基因小鼠手术连接。该方法允许通过更昔洛韦(GCV)处理有条件地消除成骨细胞。在用GCV处理15天或1.5 - 2个月的联体共生体中,在组织学标本或来自Col2.3DeltaTK联体共生体的骨髓基质细胞培养物中未检测到GFP(hOC-GFP或Col2.3GFP)表达。最后,将Col2.3GFP/Col2.3DeltaTK对用GCV处理15天,然后从GCV处理中恢复3个月。同样,在Col2.3DeltaTK联体共生体中未能检测到表达Col2.3GFP的细胞。这些观察结果,至少在该模型系统的范围内,得出骨祖细胞不易循环的结论。