Nilsson Julia, Holmberg Dan, Schmidt-Christensen Anja
Department of Experimental Medical Science, Lund University; Lund University Diabetes Centre.
Department of Experimental Medical Science, Lund University; Lund University Diabetes Centre;
J Vis Exp. 2020 Jun 11(160). doi: 10.3791/61234.
Imaging beta cells is a key step towards understanding islet transplantation. Although different imaging platforms for the recording of beta cell biology have been developed and utilized in vivo, they are limited in terms of allowing single cell resolution and continuous longitudinal recordings. Because of the transparency of the cornea, the anterior chamber of the eye (ACE) in mice is well suited to study human and mouse pancreatic islet cell biology. Here is a description of how this approach can be used to perform continuous longitudinal recordings of grafting and revascularization of individual human islet grafts. Human islet grafts are inserted into the ACE, using NOD.(Cg)-Gt(ROSA)26Sor-Rag2mice as recipients. This allows for the investigation of the expansion of recipient versus donor cells and the contribution of recipient cells in promoting the encapsulation and vascularization of the graft. Further, a step-by-step approach for image analysis and quantification of the islet volume or segmented vasculature and islet capsule forming recipient cells is outlined.
对β细胞进行成像,是了解胰岛移植的关键一步。尽管已开发出不同的成像平台用于记录体内β细胞生物学情况,但这些平台在实现单细胞分辨率和连续纵向记录方面存在局限性。由于角膜的透明度,小鼠的眼前房(ACE)非常适合用于研究人和小鼠胰岛细胞生物学。以下是关于如何利用这种方法对个体人胰岛移植物的移植和血管再生进行连续纵向记录的描述。使用NOD.(Cg)-Gt(ROSA)26Sor-Rag2小鼠作为受体,将人胰岛移植物植入ACE。这有助于研究受体细胞与供体细胞的增殖情况,以及受体细胞在促进移植物包封和血管化过程中的作用。此外,还概述了一种用于图像分析以及对胰岛体积、分段血管系统和形成胰岛囊的受体细胞进行定量分析的分步方法。