Recruitment of Rat Bone Marrow-Derived Cells to Dental Implants Immediately After Installation.

IF 1.3
Tongtong Zhang, Masako Nagasawa, Hikaru Koide, Chuta Kooanantkul, Tun Nila, Katsumi Uoshima
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Abstract

This study investigated the recruitment of bone marrow-derived cells (BMDCs) to the implant surface during the osseointegration process. Green fluorescent protein (GFP)-expressing BMDCs were transplanted into irradiated Sprague-Dawley rats to trace BMDCs following tooth extraction healing. After bone marrow transplantation, the control group exhibited maxillary bone cavities only, whereas the experimental group received implants in these cavities bilaterally. At 1, 3, 5, and 24 hours postoperation, samples were prepared for immunohistochemical staining. At 24 hours postimplantation, the cells were collected from the implant sites and analyzed using double fluorescence staining. In the experimental group, the number of GFP-positive cells gradually increased over time and was significantly greater than that in the control group at the 3- and 24-hour time points. At 24 hours after implantation, the cells around the implant surface were analyzed. Hematopoietic stem cell markers and mesenchymal stem cell markers were detected in the GFP-positive cells. These data showed that bone marrow-derived cells are recruited to the implant surface in the rats' maxillae. These findings also suggest that hematopoietic stem cells and mesenchymal stem cells derived from bone marrow are important for the establishment of osseointegration in the rats' maxillae in the very early stages. The limitations of this study include its small sample size and relatively short observation period. Future research should involve an increased number of samples and a longer observation timeline. Furthermore, investigating how these cells undergo differentiation over time is necessary.

大鼠骨髓来源的细胞在牙种植体安装后立即募集。
本研究探讨了骨整合过程中骨髓源性细胞(bmdc)在种植体表面的募集情况。将表达绿色荧光蛋白(GFP)的BMDCs移植到辐照的Sprague-Dawley大鼠体内,追踪拔牙愈合后的BMDCs。骨髓移植后,对照组只出现上颌骨腔,而实验组在这些腔内双侧植入。于术后1、3、5、24小时制备标本进行免疫组织化学染色。在植入24小时后,从植入部位收集细胞,用双荧光染色分析。实验组gfp阳性细胞数量随时间逐渐增加,在3、24小时时间点明显大于对照组。在植入24小时后,分析植入体表面周围的细胞。在gfp阳性细胞中检测到造血干细胞标志物和间充质干细胞标志物。这些数据表明,骨髓来源的细胞被招募到大鼠上颌骨的种植体表面。这些发现还表明,来源于骨髓的造血干细胞和间充质干细胞对于大鼠上颌早期骨整合的建立是重要的。本研究的局限性在于样本量小,观察期较短。未来的研究应该包括增加样本数量和更长的观察时间。此外,研究这些细胞如何随着时间的推移进行分化是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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