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[title] => [Real-time, multidimensional in vivo imaging used to investigate blood flow in mouse pancreatic islets.]
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Nyman+LR">Nyman LR , Wells KS , Head WS , McCaughey M , Ford E , Brissova M , Piston DW , Powers AC ,</a></div>
<div class="biblio_source"><h3>Source: </h3> The Journal of clinical investigation, Volume 118, p.3790-7 (2008)</div>
<h3>URL:</h3><a href="http://dx.doi.org/10.1172/JCI36209">http://dx.doi.org/10.1172/JCI36209</a>
<h3>Abstract:</h3> <p>The pancreatic islets of Langerhans are highly vascularized micro-organs that play a key role in the regulation of blood glucose homeostasis. The specific arrangement of endocrine cell types in islets suggests a coupling between morphology and function within the islet. Here, we established a line-scanning confocal microscopy approach to examine the relationship between blood flow and islet cell type arrangement by real-time in vivo imaging of intra-islet blood flow in mice. These data were used to reconstruct the in vivo 3D architecture of the islet and time-resolved blood flow patterns throughout the islet vascular bed. The results revealed 2 predominant blood flow patterns in mouse islets: inner-to-outer, in which blood perfuses the core of beta cells before the islet perimeter of non-beta cells, and top-to-bottom, in which blood perfuses the islet from one side to the other regardless of cell type. Our approach included both millisecond temporal resolution and submicron spatial resolution, allowing for real-time imaging of islet blood flow within the living mouse, which has not to our knowledge been attainable by other methods.</p>
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[biblio_authors] => [Nyman LR , Wells KS , Head WS , McCaughey M , Ford E , Brissova M , Piston DW , Powers AC ,]
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[biblio_abst_e] => [<p>The pancreatic islets of Langerhans are highly vascularized micro-organs that play a key role in the regulation of blood glucose homeostasis. The specific arrangement of endocrine cell types in islets suggests a coupling between morphology and function within the islet. Here, we established a line-scanning confocal microscopy approach to examine the relationship between blood flow and islet cell type arrangement by real-time in vivo imaging of intra-islet blood flow in mice. These data were used to reconstruct the in vivo 3D architecture of the islet and time-resolved blood flow patterns throughout the islet vascular bed. The results revealed 2 predominant blood flow patterns in mouse islets: inner-to-outer, in which blood perfuses the core of beta cells before the islet perimeter of non-beta cells, and top-to-bottom, in which blood perfuses the islet from one side to the other regardless of cell type. Our approach included both millisecond temporal resolution and submicron spatial resolution, allowing for real-time imaging of islet blood flow within the living mouse, which has not to our knowledge been attainable by other methods.</p>]
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Nyman+LR">Nyman LR , Wells KS , Head WS , McCaughey M , Ford E , Brissova M , Piston DW , Powers AC ,</a></div>
<div class="biblio_source"><h3>Source: </h3> The Journal of clinical investigation, Volume 118, p.3790-7 (2008)</div>
<h3>URL:</h3><a href="http://dx.doi.org/10.1172/JCI36209">http://dx.doi.org/10.1172/JCI36209</a>
<h3>Abstract:</h3> <p>The pancreatic islets of Langerhans are highly vascularized micro-organs that play a key role in the regulation of blood glucose homeostasis. The specific arrangement of endocrine cell types in islets suggests a coupling between morphology and function within the islet. Here, we established a line-scanning confocal microscopy approach to examine the relationship between blood flow and islet cell type arrangement by real-time in vivo imaging of intra-islet blood flow in mice. These data were used to reconstruct the in vivo 3D architecture of the islet and time-resolved blood flow patterns throughout the islet vascular bed. The results revealed 2 predominant blood flow patterns in mouse islets: inner-to-outer, in which blood perfuses the core of beta cells before the islet perimeter of non-beta cells, and top-to-bottom, in which blood perfuses the islet from one side to the other regardless of cell type. Our approach included both millisecond temporal resolution and submicron spatial resolution, allowing for real-time imaging of islet blood flow within the living mouse, which has not to our knowledge been attainable by other methods.</p>
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Nyman+LR">Nyman LR , Wells KS , Head WS , McCaughey M , Ford E , Brissova M , Piston DW , Powers AC ,</a></div>
<div class="biblio_source"><h3>Source: </h3> The Journal of clinical investigation, Volume 118, p.3790-7 (2008)</div>
<h3>URL:</h3><a href="http://dx.doi.org/10.1172/JCI36209">http://dx.doi.org/10.1172/JCI36209</a>
<h3>Abstract:</h3> <p>The pancreatic islets of Langerhans are highly vascularized micro-organs that play a key role in the regulation of blood glucose homeostasis. The specific arrangement of endocrine cell types in islets suggests a coupling between morphology and function within the islet. Here, we established a line-scanning confocal microscopy approach to examine the relationship between blood flow and islet cell type arrangement by real-time in vivo imaging of intra-islet blood flow in mice. These data were used to reconstruct the in vivo 3D architecture of the islet and time-resolved blood flow patterns throughout the islet vascular bed. The results revealed 2 predominant blood flow patterns in mouse islets: inner-to-outer, in which blood perfuses the core of beta cells before the islet perimeter of non-beta cells, and top-to-bottom, in which blood perfuses the islet from one side to the other regardless of cell type. Our approach included both millisecond temporal resolution and submicron spatial resolution, allowing for real-time imaging of islet blood flow within the living mouse, which has not to our knowledge been attainable by other methods.</p>
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