Confocal Laser Scanning Microscopy of Calcium Dynamics in Acute Mouse Pancreatic Tissue Slices
Author(s) -
Andraž Stožer,
Jurij Dolenšek,
Lidija Križančić Bombek,
Viljem Pohorec,
Marjan Slak Rupnik,
Maša Skelin Klemen
Publication year - 2021
Publication title -
journal of visualized experiments
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 91
ISSN - 1940-087X
DOI - 10.3791/62293
Subject(s) - confocal , confocal microscopy , paracrine signalling , microbiology and biotechnology , calcium , microscopy , calcium in biology , pancreatic islets , biophysics , enteroendocrine cell , biology , islet , intracellular , pathology , chemistry , endocrine system , endocrinology , biochemistry , medicine , optics , receptor , physics , organic chemistry , hormone , insulin
The acute mouse pancreatic tissue slice is a unique in situ preparation with preserved intercellular communication and tissue architecture that entails significantly fewer preparation-induced changes than isolated islets, acini, ducts, or dispersed cells described in typical in vitro studies. By combining the acute pancreatic tissue slice with live-cell calcium imaging in confocal laser scanning microscopy (CLSM), calcium signals can be studied in a large number of endocrine and exocrine cells simultaneously, with a single-cell or even subcellular resolution. The sensitivity permits the detection of changes and enables the study of intercellular waves and functional connectivity as well as the study of the dependence of physiological responses of cells on their localization within the islet and paracrine relationship with other cells. Finally, from the perspective of animal welfare, recording signals from a large number of cells at a time lowers the number of animals required in experiments, contributing to the 3R-replacement, reduction, and refinement-principle.
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