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骨髓间充质干细胞经系统给药在牙周组织再生中的作用。

The role of systemically delivered bone marrow-derived mesenchymal stem cells in the regeneration of periodontal tissues.

出版信息

Int J Oral Maxillofac Implants. 2013 Nov-Dec;28(6):e503-11. doi: 10.11607/jomi.te31.

Abstract

PURPOSE

Recent studies have shown that periodontal ligament stem cells (PDLSCs) play a key role in periodontal regeneration. However, the origin of these cells remains unclear. Meanwhile, bone marrow is thought to be the most common source of adult stem cells in many tissues and organs. Thus, the present investigation sought to determine whether systemically delivered bone marrow-derived mesenchymal stem cells (BM-MSCs) could participate in periodontal regeneration and differentiate into periodontal-specific cells and to explore the origin of PDLSCs.

METHODS

Enhanced green fluorescent protein (EGFP)-labeled BMMSCs were delivered into lethally irradiated rats by intra-bone marrow (IBM) transplantation. Four weeks after transplantation, periodontal defects with and without infection of anaerobic cultured Porphyromonas gingivalis were established. The animals were killed 1, 2, 4, or 6 weeks after periodontal defect surgery. Histomorphologic analysis, direct observation with the fluorescence microscope, and immunohistochemical staining were performed to evaluate the localization and differentiation of BM-MSCs.

RESULTS

EGFP-positive BM-MSCs could be observed as early as 1 week after surgery, and the number of EGFP-positive cells reached a maximum at 2 weeks. Meanwhile, EGFP-positive cells were observed in the newly formed bone, PDL, and cementum 4 weeks after surgery. Immunohistochemical staining verified that EGFP-positive BM-MSCs could differentiate into osteoblasts.

CONCLUSIONS

These findings provide direct evidence that BM-MSCs can participate in and modulate periodontal regeneration.

摘要

目的

最近的研究表明,牙周膜干细胞(PDLSCs)在牙周再生中起着关键作用。然而,这些细胞的来源尚不清楚。同时,骨髓被认为是许多组织和器官中成年干细胞的最常见来源。因此,本研究旨在确定是否可以通过骨髓内(IBM)移植将全身输送的骨髓间充质干细胞(BM-MSCs)用于牙周再生,并分化为牙周特异性细胞,并探讨 PDLSCs 的起源。

方法

将增强型绿色荧光蛋白(EGFP)标记的 BMMSCs 通过骨髓内移植输送到致死性辐射的大鼠体内。移植后 4 周,建立有和没有厌氧培养牙龈卟啉单胞菌感染的牙周缺损。牙周缺损手术后 1、2、4 或 6 周处死动物。进行组织形态学分析、荧光显微镜直接观察和免疫组织化学染色,以评估 BM-MSCs 的定位和分化。

结果

手术后 1 周即可观察到 EGFP 阳性 BM-MSCs,并且 EGFP 阳性细胞的数量在 2 周时达到最大值。同时,手术后 4 周可在新形成的骨、牙周膜和牙骨质中观察到 EGFP 阳性细胞。免疫组织化学染色证实 EGFP 阳性 BM-MSCs 可分化为成骨细胞。

结论

这些发现提供了直接证据,证明 BM-MSCs 可以参与并调节牙周再生。

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