Cell polarity defines three distinct domains in pancreatic beta cells
Author(s) -
Wan Jun Gan,
Michael Zavortink,
Christine Ludick,
Rachel Templin,
Robyn Webb,
Richard I. Webb,
Wei Ma,
Philip Poronnik,
Robert G. Parton,
Herbert Y. Gaisano,
Annette M. Shewan,
Peter Thorn
Publication year - 2016
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.185116
Subject(s) - biology , microbiology and biotechnology , cilium , beta (programming language) , islet , cell polarity , extracellular , cell , anatomy , biochemistry , endocrinology , insulin , computer science , programming language
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.
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