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Evaluation of Arteriolar Smooth Muscle Cell Function in an Ex Vivo Microvascular Network Model
An emerging challenge in tissue engineering biomimetic models is recapitulating the physiological complexity associated with real tissues. Recently, our laboratory introduced the rat mesentery culture model as an ex vivo experimental platform for investigating the multi-cellular dynamics involved in...
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Published in: | Scientific reports 2017-05, Vol.7 (1), p.2195-12, Article 2195 |
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description | An emerging challenge in tissue engineering biomimetic models is recapitulating the physiological complexity associated with real tissues. Recently, our laboratory introduced the rat mesentery culture model as an
ex vivo
experimental platform for investigating the multi-cellular dynamics involved in angiogenesis within an intact microvascular network using time-lapse imaging. A critical question remains whether the vessels maintain their functionality. The objective of this study was to determine whether vascular smooth muscle cells in cultured microvascular networks maintain the ability to constrict. Adult rat mesenteric tissues were harvested and cultured for three days in either MEM or MEM plus 10% serum. On Day 0 and Day 3 live microvascular networks were visualized with FITC conjugated BSI-lectin labeling and arteriole diameters were compared before and five minutes after topical exposure to vasoconstrictors (50 mM KCl and 20 nM Endothelin-1). Arterioles displayed a vasoconstriction response to KCl and endothelin for each experimental group. However, the Day 3 serum cultured networks were angiogenic, characterized by increased vessel density, and displayed a decreased vasoconstriction response compared to Day 0 networks. The results support the physiological relevance of the rat mesentery culture model as a biomimetic tool for investigating microvascular growth and function
ex vivo
. |
doi_str_mv | 10.1038/s41598-017-02272-4 |
format | article |
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ex vivo
experimental platform for investigating the multi-cellular dynamics involved in angiogenesis within an intact microvascular network using time-lapse imaging. A critical question remains whether the vessels maintain their functionality. The objective of this study was to determine whether vascular smooth muscle cells in cultured microvascular networks maintain the ability to constrict. Adult rat mesenteric tissues were harvested and cultured for three days in either MEM or MEM plus 10% serum. On Day 0 and Day 3 live microvascular networks were visualized with FITC conjugated BSI-lectin labeling and arteriole diameters were compared before and five minutes after topical exposure to vasoconstrictors (50 mM KCl and 20 nM Endothelin-1). Arterioles displayed a vasoconstriction response to KCl and endothelin for each experimental group. However, the Day 3 serum cultured networks were angiogenic, characterized by increased vessel density, and displayed a decreased vasoconstriction response compared to Day 0 networks. The results support the physiological relevance of the rat mesentery culture model as a biomimetic tool for investigating microvascular growth and function
ex vivo
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ex vivo
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ex vivo
.</description><subject>13/106</subject><subject>13/107</subject><subject>631/1647/767/1657</subject><subject>631/61/2049</subject><subject>Angiogenesis</subject><subject>Animal models</subject><subject>Animals</subject><subject>Arterioles</subject><subject>Arterioles - cytology</subject><subject>Biomimetics</subject><subject>Cell culture</subject><subject>Chlorides</subject><subject>Endothelin 1</subject><subject>Endothelins</subject><subject>Humanities and Social Sciences</subject><subject>Male</subject><subject>Mesentery</subject><subject>Microvasculature</subject><subject>Microvessels</subject><subject>Models, Biological</subject><subject>multidisciplinary</subject><subject>Muscle, Smooth, Vascular - cytology</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Neovascularization, Physiologic</subject><subject>Physiology</subject><subject>Potassium chloride</subject><subject>Rats</subject><subject>Rodents</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Smooth muscle</subject><subject>Time-Lapse Imaging</subject><subject>Tissue engineering</subject><subject>Vasoconstriction</subject><subject>Vasoconstrictors</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kk1v1DAQhiMEolXpH-CALHHhEvDHOLEvSNVqC5W6cODjiDVx7G2WbFzsZIF_j3dTqi0SvtjyvPOMZ_wWxXNGXzMq1JsETGpVUlaXlPOal_CoOOUUZMkF54-PzifFeUobmpfkGph-WpxwJXmlpD4tvi132E84dmEgwZOLOLrYhR4j-bQNYbwhqynZ3pGF63tyOQ32oOwGggNZ_iJfu10gq87GsMNkp33eBzf-DPE7WYXW9c-KJx775M7v9rPiy-Xy8-J9ef3x3dXi4rq0EuhYgrWq1oyrWlaNqHSF3raUobYNNo5L8E74yqOQsm6FcJZW1kJb-xpAA63EWXE1c9uAG3Mbuy3G3yZgZw4XIa4NxrHLnRjLtK4FSN6gAg8aWw-oWKsb3TJAl1lvZ9bt1Gxda90wRuwfQB9Ghu7GrMPOSBAKGM-AV3eAGH5MLo1m2yWbB4iDC1MyTFOqBFdcZenLf6SbMMUhjyqrpASVG94D-azKc04pOn__GEbN3g1mdoPJbjAHNxjISS-O27hP-fv3WSBmQcqhYe3iUe3_Y_8AGK3ADQ</recordid><startdate>20170519</startdate><enddate>20170519</enddate><creator>Motherwell, Jessica M.</creator><creator>Azimi, Mohammad S.</creator><creator>Spicer, Kristine</creator><creator>Alves, Natascha G.</creator><creator>Hodges, Nicholas A.</creator><creator>Breslin, Jerome W.</creator><creator>Katakam, Prasad V. 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G.</au><au>Murfee, Walter L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of Arteriolar Smooth Muscle Cell Function in an Ex Vivo Microvascular Network Model</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2017-05-19</date><risdate>2017</risdate><volume>7</volume><issue>1</issue><spage>2195</spage><epage>12</epage><pages>2195-12</pages><artnum>2195</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>An emerging challenge in tissue engineering biomimetic models is recapitulating the physiological complexity associated with real tissues. Recently, our laboratory introduced the rat mesentery culture model as an
ex vivo
experimental platform for investigating the multi-cellular dynamics involved in angiogenesis within an intact microvascular network using time-lapse imaging. A critical question remains whether the vessels maintain their functionality. The objective of this study was to determine whether vascular smooth muscle cells in cultured microvascular networks maintain the ability to constrict. Adult rat mesenteric tissues were harvested and cultured for three days in either MEM or MEM plus 10% serum. On Day 0 and Day 3 live microvascular networks were visualized with FITC conjugated BSI-lectin labeling and arteriole diameters were compared before and five minutes after topical exposure to vasoconstrictors (50 mM KCl and 20 nM Endothelin-1). Arterioles displayed a vasoconstriction response to KCl and endothelin for each experimental group. However, the Day 3 serum cultured networks were angiogenic, characterized by increased vessel density, and displayed a decreased vasoconstriction response compared to Day 0 networks. The results support the physiological relevance of the rat mesentery culture model as a biomimetic tool for investigating microvascular growth and function
ex vivo
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subjects | 13/106 13/107 631/1647/767/1657 631/61/2049 Angiogenesis Animal models Animals Arterioles Arterioles - cytology Biomimetics Cell culture Chlorides Endothelin 1 Endothelins Humanities and Social Sciences Male Mesentery Microvasculature Microvessels Models, Biological multidisciplinary Muscle, Smooth, Vascular - cytology Myocytes, Smooth Muscle - metabolism Neovascularization, Physiologic Physiology Potassium chloride Rats Rodents Science Science (multidisciplinary) Smooth muscle Time-Lapse Imaging Tissue engineering Vasoconstriction Vasoconstrictors |
title | Evaluation of Arteriolar Smooth Muscle Cell Function in an Ex Vivo Microvascular Network Model |
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