Gan Wan J, Zavortink Michael, Ludick Christine, Templin Rachel, Webb Robyn, Webb Richard, Ma Wei, Poronnik Philip, Parton Robert G, Gaisano Herbert Y, Shewan Annette M, Thorn Peter
School of Biomedical Sciences, University of Queensland, St Lucia, Queensland 4072, Australia.
Charles Perkins Centre, John Hopkins Drive, University of Sydney, Camperdown, New South Wales, 2050, Australia.
J Cell Sci. 2017 Jan 1;130(1):143-151. doi: 10.1242/jcs.185116. Epub 2016 Feb 26.
The structural organisation of pancreatic β-cells in the islets of Langerhans is relatively unknown. Here, using three-dimensional (3D) two-photon, 3D confocal and 3D block-face serial electron microscopy, we demonstrate a consistent in situ polarisation of β-cells and define three distinct cell surface domains. An apical domain located at the vascular apogee of β-cells, defined by the location of PAR-3 (also known as PARD3) and ZO-1 (also known as TJP1), delineates an extracellular space into which adjacent β-cells project their primary cilia. A separate lateral domain, is enriched in scribble and Dlg, and colocalises with E-cadherin and GLUT2 (also known as SLC2A2). Finally, a distinct basal domain, where the β-cells contact the islet vasculature, is enriched in synaptic scaffold proteins such as liprin. This 3D analysis of β-cells within intact islets, and the definition of distinct domains, provides new insights into understanding β-cell structure and function.
胰岛中胰腺β细胞的结构组织相对未知。在这里,我们使用三维(3D)双光子、3D共聚焦和3D块面连续电子显微镜,证明了β细胞在原位的一致极化,并定义了三个不同的细胞表面结构域。一个顶端结构域位于β细胞的血管顶点,由PAR-3(也称为PARD3)和ZO-1(也称为TJP1)的位置定义,勾勒出一个细胞外空间,相邻的β细胞将其初级纤毛投射到该空间中。一个单独的侧向结构域富含scribble和Dlg,并与E-钙黏蛋白和GLUT2(也称为SLC2A2)共定位。最后,一个独特的基底结构域,β细胞在此处与胰岛血管接触,富含突触支架蛋白,如liprin。对完整胰岛内β细胞的这种3D分析以及不同结构域的定义,为理解β细胞的结构和功能提供了新的见解。