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In Vivo and In Situ Approach to Study Islet Microcirculation: A Mini-Review

Journal

FRONTIERS IN ENDOCRINOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2021.602620

Keywords

beta cell (β -Cell); islet; capillary; microcirculation; intravital 2-photon microscopy; 3D image analysis

Funding

  1. National Institutes of Health [DK117192, DK127786, DK020595]

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The pancreas is composed of two separate systems - the endocrine and exocrine pancreas. Treatment of diseases affecting either system may impact the overall pancreatic function, leading to different disciplines of medical professionals providing treatment. A new model suggests that islet blood flow is integrated with the surrounding exocrine capillary network, potentially offering new hypotheses for pancreatic diseases and their regulation of hormones and functions.
The pancreas is regarded as consisting of two separate organ systems, the endocrine and exocrine pancreas. While treatment of a disease with either an endocrine or exocrine pathogenesis may affect the function of the entire pancreas, the pancreatic diseases have been treated by clinicians in different medical disciplines, including endocrinologists and gastroenterologists. Islet microcirculation has long been considered to be regulated independently from that of the exocrine pancreas. A new model proposes that pancreatic islet blood flow is integrated with the surrounding exocrine capillary network. This recent model may provide revived or contrasting hypotheses to test, since the pancreatic microcirculation has critical implications for the regulation of islet hormones as well as acinar pancreas functions. In this mini-review, practical applications of in vivo and in situ studies of islet microcirculation are described with a specific emphasis on large-scale data analysis to ensure sufficient sample size accounting for known islet heterogeneity. For in vivo small animal studies, intravital microscopy based on two-photon excitation microscopes is a powerful tool that enables capturing the flow direction and speed of individual fluorescent-labeled red blood cells. Complementarily, for structural analysis of blood vessels, the recent technical advancements of confocal microscopy and tissue clearing have enabled us to image the three-dimensional network structure in thick tissue slices.

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