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In vivo longitudinal visualization of bone marrow engraftment process in mouse calvaria using two-photon microscopy

机译:使用双光子显微镜的小鼠Calvaria骨髓植入过程的体内纵向可视化

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Intravital microscopy of mouse calvarial bone marrow (BM) is a powerful method for studying hematopoietic stem cells (HSCs) and the BM microenvironment at the cellular level. However, the current method used to access the mouse calvaria allows for only a few imaging times in the same mouse because of scar formation and inflammation induced by multiple surgeries. Longitudinal imaging of the BM may help better understand its microenvironment. In this study, a mouse calvarial window model was developed for longitudinal imaging that involves attaching a cover glass window onto the mouse calvaria and sealing the surrounding exposed area with cyanoacrylate glue and dental cement. The model was used for the longitudinal two-photon microscopy (TPM) imaging of the BM engraftment process. The same BM cavity sites were imaged multiple times over 4 weeks after BM transplantation (BMT). Temporal changes in the BM microenvironment, such as the reconstitution of transplanted BM cells and the recovery of vasculature, were observed and analysed qualitatively and quantitatively. Longitudinal intravital microscopy using the mouse calvarial window model was successfully demonstrated and may be useful for further BM studies.
机译:小鼠颅骨骨髓(BM)的嗜睡显微镜是研究造血干细胞(HSC)和细胞水平的BM微环境的强大方法。然而,用于访问鼠标calvaria的当前方法由于多种手术诱导的瘢痕形成和炎症,仅在同一鼠标中仅允许几次成像时间。 BM的纵向成像可能有助于更好地理解其微环境。在这项研究中,开发了一种用于纵向成像的鼠标颅窗模型,涉及将盖子玻璃窗连接到小鼠Calvaria上并用氰基丙烯酸糖胶和牙科水泥密封周围的暴露区域。该模型用于BM植入过程的纵向二光子显微镜(TPM)成像。在BM移植(BMT)后4周内多次成像相同的BM腔位点。 BM微环境中的时间变化,例如移植的BM细胞重构和脉管系统的回收,定性和定量分析。使用鼠标颅骨窗口模型的纵向脊柱体显微镜经过证明,可用于进一步的BM研究。

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