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体内鉴定牙周祖细胞。

In vivo identification of periodontal progenitor cells.

机构信息

Department of Reconstructive Sciences, University of Connecticut Health Center, Farmington, CT, USA.

出版信息

J Dent Res. 2013 Aug;92(8):709-15. doi: 10.1177/0022034513493434. Epub 2013 Jun 4.

Abstract

The periodontal ligament contains progenitor cells; however, their identity and differentiation potential in vivo remain poorly characterized. Previous results have suggested that periodontal tissue progenitors reside in perivascular areas. Therefore, we utilized a lineage-tracing approach to identify and track periodontal progenitor cells from the perivascular region in vivo. We used an alpha-smooth muscle actin (αSMA) promoter-driven and tamoxifen-inducible Cre system (αSMACreERT2) that, in combination with a reporter mouse line (Ai9), permanently labels a cell population, termed 'SMA9'. To trace the differentiation of SMA9-labeled cells into osteoblasts/cementoblasts, we utilized a Col2.3GFP transgene, while expression of Scleraxis-GFP was used to follow differentiation into periodontal ligament fibroblasts during normal tissue formation and remodeling following injury. In uninjured three-week-old SMA9 mice, tamoxifen labeled a small population of cells in the periodontal ligament that expanded over time, particularly in the apical region of the root. By 17 days and 7 weeks after labeling, some SMA9-labeled cells expressed markers indicating differentiation into mature lineages, including cementocytes. Following injury, SMA9 cells expanded, and differentiated into cementoblasts, osteoblasts, and periodontal ligament fibroblasts. SMA9-labeled cells represent a source of progenitors that can give rise to mature osteoblasts, cementoblasts, and fibroblasts within the periodontium.

摘要

牙周韧带含有祖细胞;然而,其在体内的特性和分化潜能仍未得到很好的描述。先前的研究结果表明,牙周组织祖细胞位于血管周围区域。因此,我们利用谱系追踪方法来鉴定和追踪体内血管周围区域的牙周祖细胞。我们使用了一个α平滑肌肌动蛋白(αSMA)启动子驱动和他莫昔芬诱导的 Cre 系统(αSMACreERT2),该系统与一个报告鼠系(Ai9)结合,永久性地标记了一个细胞群体,称为“SMA9”。为了追踪 SMA9 标记细胞向成骨细胞/成牙骨质细胞的分化,我们利用了 Col2.3GFP 转基因,而 Scleraxis-GFP 的表达则用于在正常组织形成和损伤后重塑过程中追踪 SMA9 标记细胞分化为牙周韧带成纤维细胞。在未受伤的三周龄 SMA9 小鼠中,他莫昔芬标记了牙周韧带中一小部分细胞,这些细胞随时间推移而扩张,特别是在根的根尖区域。在标记后的 17 天和 7 周,一些 SMA9 标记的细胞表达了分化为成熟谱系的标志物,包括成牙骨质细胞。损伤后,SMA9 细胞扩增,并分化为成牙骨质细胞、成骨细胞和牙周韧带成纤维细胞。SMA9 标记的细胞代表了一种祖细胞的来源,可以在牙周组织中产生成熟的成骨细胞、成牙骨质细胞和成纤维细胞。

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