Assessment of Human Pancreatic Islet Architecture and Composition by Laser Scanning Confocal Microscopy
Author(s) -
Marcela Briššová,
Michael J. Fowler,
Wendell E. Nicholson,
Anita Chu,
Boaz Hirshberg,
David M. Harlan,
Alvin C. Powers
Publication year - 2005
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1369/jhc.5c6684.2005
Subject(s) - islet , pancreatic islets , pancreas , transplantation , biology , confocal , cell , confocal microscopy , microbiology and biotechnology , medicine , endocrinology , insulin , biochemistry , geometry , mathematics
The recent success of pancreatic islet transplantation has generated considerable enthusiasm. To better understand the quality and characteristics of human islets used for transplantation, we performed detailed analysis of islet architecture and composition using confocal laser scanning microscopy. Human islets from six separate isolations provided by three different islet isolation centers were compared with isolated mouse and non-human primate islets. As expected from histological sections of murine pancreas, in isolated murine islets α and δ cells resided at the periphery of the β-cell core. However, human islets were markedly different in that α, β, and δ cells were dispersed throughout the islet. This pattern of cell distribution was present in all human islet preparations and islets of various sizes and was also seen in histological sections of human pancreas. The architecture of isolated non-human primate islets was very similar to that of human islets. Using an image analysis program, we calculated the volume of α, β, and δ cells. In contrast to murine islets, we found that populations of islet cell types varied considerably in human islets. The results indicate that human islets not only are quite heterogeneous in terms of cell composition but also have a substantially different architecture from widely studied murine islets.
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