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Mechanisms of bone repair and regeneration.骨修复与再生的机制。
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Genomic profiling of mesenchymal stem cells.间充质干细胞的基因组分析
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Circulating endothelial/skeletal progenitor cells for bone regeneration and healing.用于骨再生和愈合的循环内皮/骨骼祖细胞。
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在软骨内骨化过程中软骨膜中 Thy-1 阳性细胞的定位。

Localization of Thy-1-positive cells in the perichondrium during endochondral ossification.

机构信息

Department of Oral Histology, Matsumoto Dental University, 1780 Gobara Hirooka, Shiojiri 399-0781, Japan.

出版信息

J Histochem Cytochem. 2010 May;58(5):455-62. doi: 10.1369/jhc.2010.955393. Epub 2010 Feb 1.

DOI:10.1369/jhc.2010.955393
PMID:20124093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2857817/
Abstract

We elucidated the localization of Thy-1-positive cells in the perichondrium of fetal rat limb bones to clarify the distribution of osteogenic cells in the process of endochondral ossification. We also examined the formation of calcified bone-like matrices by isolated perichondrial cells in vitro. At embryonic day (E) 15.5, when the cartilage primodia were formed, immunoreactivity for Thy-1 was detected in cells of the perichondrium adjacent to the zone of hypertrophic chondrocytes. At E17.5, when the bone collar formation and the vascular invasion were initiated, fibroblast-like cells at the sites of vascular invasion, as well as in the perichondrium, showed Thy-1 labeling. Double immunostaining for Thy-1 and osterix revealed that Thy-1 was not expressed in the osterix-positive osteoblasts. Electron microscopic analysis revealed that Thy-1-positive cells in the zone of hypertrophic chondrocytes came in contact with blood vessels. Perichondrial cells isolated from limb bones showed alkaline phosphatase activity and formed calcified bone-like matrices after 4 weeks in osteogenic medium. RT-PCR demonstrated that Thy-1 expression decreased as calcified nodules formed. Conversely, the expression of osteogenic marker genes Runx2, osterix, and osteocalcin increased. These results indicate that Thy-1 is a good marker for characterizing osteoprogenitor cells.

摘要

我们阐明了胎鼠肢骨软骨膜中 Thy-1 阳性细胞的定位,以阐明骺软骨内成骨过程中成骨细胞的分布。我们还研究了分离的软骨膜细胞在体外形成钙化骨样基质的情况。在胚胎第 15.5 天(E),当软骨原基形成时,在靠近肥大软骨细胞区的软骨膜细胞中检测到 Thy-1 的免疫反应性。在 E17.5 天,当骨领形成和血管浸润开始时,血管浸润部位和成骨细胞周围的成纤维细胞样细胞显示 Thy-1 标记。Thy-1 和osterix 的双重免疫染色表明 Thy-1 不在 osterix 阳性成骨细胞中表达。电镜分析显示,肥大软骨细胞区的 Thy-1 阳性细胞与血管接触。从肢骨中分离的软骨膜细胞在成骨培养基中培养 4 周后表现出碱性磷酸酶活性并形成钙化骨样基质。RT-PCR 表明,随着钙化结节的形成,Thy-1 的表达减少。相反,成骨标志物基因 Runx2、osterix 和骨钙素的表达增加。这些结果表明 Thy-1 是一种很好的成骨前体细胞标志物。