Elevated arterial shear rate increases indexes of endothelial cell autophagy and nitric oxide synthase activation in humans
Continuous laminar shear stress increases the process of autophagy, activates endothelial nitric oxide (NO) synthase phosphorylation at serine 1177 (p-eNOS ), and generates NO in bovine and human arterial endothelial cells (ECs) compared with static controls. However, the translational relevance of...
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creator | Park, Seul-Ki La Salle, D Taylor Cerbie, James Cho, Jae Min Bledsoe, Amber Nelson, Ashley Morgan, David E Richardson, Russell S Shiu, Yan-Ting Boudina, Sihem Trinity, Joel D Symons, J David |
description | Continuous laminar shear stress increases the process of autophagy, activates endothelial nitric oxide (NO) synthase phosphorylation at serine 1177 (p-eNOS
), and generates NO in bovine and human arterial endothelial cells (ECs) compared with static controls. However, the translational relevance of these findings has not been explored. In the current study, primary ECs were collected from the radial artery of 7 men using sterile J-wires before (Pre) and after (Post) 60 min of rhythmic handgrip exercise (HG) performed with the same arm. After ECs were identified by positive costaining for vascular endothelial cadherin and 4',6'-diamidino-2-phenylindole, immunofluorescent antibodies were used to assess indices of autophagy, NO generation, and superoxide anion (O
) production. Commercially available primary human arterial ECs were stained and processed in parallel to serve as controls. All end points were evaluated using 75 ECs from each subject. Relative to Pre-HG, HG elevated arterial shear rate ( P < 0.05) ~3-fold, whereas heart rate, arterial pressure, and cardiac output were not altered. Compared with values obtained from ECs Pre-HG, Post-HG ECs displayed increased ( P < 0.05) expression of p-eNOS
, NO generation, O
production, BECLIN1, microtubule-associated proteins 1A/1B light chain 3B, autophagy-related gene 3, and lysosomal-associated membrane protein 2A and decreased ( P < 0.05) expression (i.e., enhanced degradation) of the adaptor protein p62/sequestosome-1. These novel findings provide evidence that elevated arterial shear rate associated with functional hyperemia initiates autophagy, activates p-eNOS
, and increases NO and O
generation in primary human ECs. NEW & NOTEWORTHY Previously, our group reported in bovine arterial and human arterial endothelial cells (ECs) that shear stress initiates trafficking of the autophagosome to the lysosome and increases endothelial nitric oxide (NO) synthase phosphorylation at serine 1177, NO generation, and O
production. Here, the translational relevance of these findings is documented. Specifically, functional hyperemia induced by rhythmic handgrip exercise elevates arterial shear rate to an extent that increases indices of autophagy, NO generation, and O
production in primary arterial ECs collected from healthy men. |
doi_str_mv | 10.1152/ajpheart.00561.2018 |
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), and generates NO in bovine and human arterial endothelial cells (ECs) compared with static controls. However, the translational relevance of these findings has not been explored. In the current study, primary ECs were collected from the radial artery of 7 men using sterile J-wires before (Pre) and after (Post) 60 min of rhythmic handgrip exercise (HG) performed with the same arm. After ECs were identified by positive costaining for vascular endothelial cadherin and 4',6'-diamidino-2-phenylindole, immunofluorescent antibodies were used to assess indices of autophagy, NO generation, and superoxide anion (O
) production. Commercially available primary human arterial ECs were stained and processed in parallel to serve as controls. All end points were evaluated using 75 ECs from each subject. Relative to Pre-HG, HG elevated arterial shear rate ( P < 0.05) ~3-fold, whereas heart rate, arterial pressure, and cardiac output were not altered. Compared with values obtained from ECs Pre-HG, Post-HG ECs displayed increased ( P < 0.05) expression of p-eNOS
, NO generation, O
production, BECLIN1, microtubule-associated proteins 1A/1B light chain 3B, autophagy-related gene 3, and lysosomal-associated membrane protein 2A and decreased ( P < 0.05) expression (i.e., enhanced degradation) of the adaptor protein p62/sequestosome-1. These novel findings provide evidence that elevated arterial shear rate associated with functional hyperemia initiates autophagy, activates p-eNOS
, and increases NO and O
generation in primary human ECs. NEW & NOTEWORTHY Previously, our group reported in bovine arterial and human arterial endothelial cells (ECs) that shear stress initiates trafficking of the autophagosome to the lysosome and increases endothelial nitric oxide (NO) synthase phosphorylation at serine 1177, NO generation, and O
production. Here, the translational relevance of these findings is documented. Specifically, functional hyperemia induced by rhythmic handgrip exercise elevates arterial shear rate to an extent that increases indices of autophagy, NO generation, and O
production in primary arterial ECs collected from healthy men.</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00561.2018</identifier><identifier>PMID: 30412436</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Adult ; Antibodies ; Arteries - cytology ; Arteries - metabolism ; Arteries - physiology ; Autophagy ; Blood pressure ; Cadherins ; Cardiac output ; Cells, Cultured ; Endothelial cells ; Endothelial Cells - metabolism ; Endothelium, Vascular - cytology ; Endothelium, Vascular - metabolism ; Exercise ; Hand Strength ; Heart rate ; Humans ; Hyperemia ; Male ; Membrane proteins ; Microtubule-associated proteins ; Nitric oxide ; Nitric Oxide - metabolism ; Nitric Oxide Synthase Type III - metabolism ; Nitric-oxide synthase ; Phagocytosis ; Phosphorylation ; Proteins ; Rapid Report ; Rhythms ; Serine ; Shear rate ; Shear stress ; Superoxide</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2019-01, Vol.316 (1), p.H106-H112</ispartof><rights>Copyright American Physiological Society Jan 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-4df159abcddcf94a327f95566e7b066a9b5cb69085676c3f561fc2c83453f3183</citedby><cites>FETCH-LOGICAL-c433t-4df159abcddcf94a327f95566e7b066a9b5cb69085676c3f561fc2c83453f3183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30412436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Seul-Ki</creatorcontrib><creatorcontrib>La Salle, D Taylor</creatorcontrib><creatorcontrib>Cerbie, James</creatorcontrib><creatorcontrib>Cho, Jae Min</creatorcontrib><creatorcontrib>Bledsoe, Amber</creatorcontrib><creatorcontrib>Nelson, Ashley</creatorcontrib><creatorcontrib>Morgan, David E</creatorcontrib><creatorcontrib>Richardson, Russell S</creatorcontrib><creatorcontrib>Shiu, Yan-Ting</creatorcontrib><creatorcontrib>Boudina, Sihem</creatorcontrib><creatorcontrib>Trinity, Joel D</creatorcontrib><creatorcontrib>Symons, J David</creatorcontrib><title>Elevated arterial shear rate increases indexes of endothelial cell autophagy and nitric oxide synthase activation in humans</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>Continuous laminar shear stress increases the process of autophagy, activates endothelial nitric oxide (NO) synthase phosphorylation at serine 1177 (p-eNOS
), and generates NO in bovine and human arterial endothelial cells (ECs) compared with static controls. However, the translational relevance of these findings has not been explored. In the current study, primary ECs were collected from the radial artery of 7 men using sterile J-wires before (Pre) and after (Post) 60 min of rhythmic handgrip exercise (HG) performed with the same arm. After ECs were identified by positive costaining for vascular endothelial cadherin and 4',6'-diamidino-2-phenylindole, immunofluorescent antibodies were used to assess indices of autophagy, NO generation, and superoxide anion (O
) production. Commercially available primary human arterial ECs were stained and processed in parallel to serve as controls. All end points were evaluated using 75 ECs from each subject. Relative to Pre-HG, HG elevated arterial shear rate ( P < 0.05) ~3-fold, whereas heart rate, arterial pressure, and cardiac output were not altered. Compared with values obtained from ECs Pre-HG, Post-HG ECs displayed increased ( P < 0.05) expression of p-eNOS
, NO generation, O
production, BECLIN1, microtubule-associated proteins 1A/1B light chain 3B, autophagy-related gene 3, and lysosomal-associated membrane protein 2A and decreased ( P < 0.05) expression (i.e., enhanced degradation) of the adaptor protein p62/sequestosome-1. These novel findings provide evidence that elevated arterial shear rate associated with functional hyperemia initiates autophagy, activates p-eNOS
, and increases NO and O
generation in primary human ECs. NEW & NOTEWORTHY Previously, our group reported in bovine arterial and human arterial endothelial cells (ECs) that shear stress initiates trafficking of the autophagosome to the lysosome and increases endothelial nitric oxide (NO) synthase phosphorylation at serine 1177, NO generation, and O
production. Here, the translational relevance of these findings is documented. Specifically, functional hyperemia induced by rhythmic handgrip exercise elevates arterial shear rate to an extent that increases indices of autophagy, NO generation, and O
production in primary arterial ECs collected from healthy men.</description><subject>Adult</subject><subject>Antibodies</subject><subject>Arteries - cytology</subject><subject>Arteries - metabolism</subject><subject>Arteries - physiology</subject><subject>Autophagy</subject><subject>Blood pressure</subject><subject>Cadherins</subject><subject>Cardiac output</subject><subject>Cells, Cultured</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - metabolism</subject><subject>Endothelium, Vascular - cytology</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Exercise</subject><subject>Hand Strength</subject><subject>Heart rate</subject><subject>Humans</subject><subject>Hyperemia</subject><subject>Male</subject><subject>Membrane proteins</subject><subject>Microtubule-associated proteins</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase Type III - metabolism</subject><subject>Nitric-oxide synthase</subject><subject>Phagocytosis</subject><subject>Phosphorylation</subject><subject>Proteins</subject><subject>Rapid Report</subject><subject>Rhythms</subject><subject>Serine</subject><subject>Shear rate</subject><subject>Shear stress</subject><subject>Superoxide</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUuLFDEUhYMoTk_rLxAk4MZNtUluJVW1EWQYHWHAja5DKo-pNNVJm6SGafzzppwH6uqG3HO_m5OD0BtKdpRy9kHtj5NVqewI4YLuGKH9M7SpHdZQDsNztCEgoBEU-Bk6z3lPqrAT8BKdAWkpa0Fs0K_L2d6qYg2uJJu8mnFeqTjVS-yDTlZlm-vJ2Ltao8M2mFgmO69abecZq6XE46RuTlgFg4MvyWsc77yxOJ9CmSoAK1183eNjqCg8LQcV8iv0wqk529cPdYt-fL78fnHVXH_78vXi03WjW4DStMZRPqhRG6Pd0CpgnRs4F8J2IxFCDSPXoxhIz0UnNLj6GU4z3UPLwQHtYYs-3nOPy3iwRttQkprlMfmDSicZlZf_doKf5E28laKDlvSsAt4_AFL8udhc5MHn1boKNi5ZMgqMAe9r3aJ3_0n3cUmh2quqjrO-xkSqCu5VOsWck3VPj6FEruHKx3Dln3DlGm6devu3j6eZxzThN914pTM</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Park, Seul-Ki</creator><creator>La Salle, D Taylor</creator><creator>Cerbie, James</creator><creator>Cho, Jae Min</creator><creator>Bledsoe, Amber</creator><creator>Nelson, Ashley</creator><creator>Morgan, David E</creator><creator>Richardson, Russell S</creator><creator>Shiu, Yan-Ting</creator><creator>Boudina, Sihem</creator><creator>Trinity, Joel D</creator><creator>Symons, J David</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190101</creationdate><title>Elevated arterial shear rate increases indexes of endothelial cell autophagy and nitric oxide synthase activation in humans</title><author>Park, Seul-Ki ; La Salle, D Taylor ; Cerbie, James ; Cho, Jae Min ; Bledsoe, Amber ; Nelson, Ashley ; Morgan, David E ; Richardson, Russell S ; Shiu, Yan-Ting ; Boudina, Sihem ; Trinity, Joel D ; Symons, J David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-4df159abcddcf94a327f95566e7b066a9b5cb69085676c3f561fc2c83453f3183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Antibodies</topic><topic>Arteries - cytology</topic><topic>Arteries - metabolism</topic><topic>Arteries - physiology</topic><topic>Autophagy</topic><topic>Blood pressure</topic><topic>Cadherins</topic><topic>Cardiac output</topic><topic>Cells, Cultured</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - metabolism</topic><topic>Endothelium, Vascular - cytology</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Exercise</topic><topic>Hand Strength</topic><topic>Heart rate</topic><topic>Humans</topic><topic>Hyperemia</topic><topic>Male</topic><topic>Membrane proteins</topic><topic>Microtubule-associated proteins</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide Synthase Type III - metabolism</topic><topic>Nitric-oxide synthase</topic><topic>Phagocytosis</topic><topic>Phosphorylation</topic><topic>Proteins</topic><topic>Rapid Report</topic><topic>Rhythms</topic><topic>Serine</topic><topic>Shear rate</topic><topic>Shear stress</topic><topic>Superoxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Seul-Ki</creatorcontrib><creatorcontrib>La Salle, D Taylor</creatorcontrib><creatorcontrib>Cerbie, James</creatorcontrib><creatorcontrib>Cho, Jae Min</creatorcontrib><creatorcontrib>Bledsoe, Amber</creatorcontrib><creatorcontrib>Nelson, Ashley</creatorcontrib><creatorcontrib>Morgan, David E</creatorcontrib><creatorcontrib>Richardson, Russell S</creatorcontrib><creatorcontrib>Shiu, Yan-Ting</creatorcontrib><creatorcontrib>Boudina, Sihem</creatorcontrib><creatorcontrib>Trinity, Joel D</creatorcontrib><creatorcontrib>Symons, J David</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Seul-Ki</au><au>La Salle, D Taylor</au><au>Cerbie, James</au><au>Cho, Jae Min</au><au>Bledsoe, Amber</au><au>Nelson, Ashley</au><au>Morgan, David E</au><au>Richardson, Russell S</au><au>Shiu, Yan-Ting</au><au>Boudina, Sihem</au><au>Trinity, Joel D</au><au>Symons, J David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elevated arterial shear rate increases indexes of endothelial cell autophagy and nitric oxide synthase activation in humans</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>316</volume><issue>1</issue><spage>H106</spage><epage>H112</epage><pages>H106-H112</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>Continuous laminar shear stress increases the process of autophagy, activates endothelial nitric oxide (NO) synthase phosphorylation at serine 1177 (p-eNOS
), and generates NO in bovine and human arterial endothelial cells (ECs) compared with static controls. However, the translational relevance of these findings has not been explored. In the current study, primary ECs were collected from the radial artery of 7 men using sterile J-wires before (Pre) and after (Post) 60 min of rhythmic handgrip exercise (HG) performed with the same arm. After ECs were identified by positive costaining for vascular endothelial cadherin and 4',6'-diamidino-2-phenylindole, immunofluorescent antibodies were used to assess indices of autophagy, NO generation, and superoxide anion (O
) production. Commercially available primary human arterial ECs were stained and processed in parallel to serve as controls. All end points were evaluated using 75 ECs from each subject. Relative to Pre-HG, HG elevated arterial shear rate ( P < 0.05) ~3-fold, whereas heart rate, arterial pressure, and cardiac output were not altered. Compared with values obtained from ECs Pre-HG, Post-HG ECs displayed increased ( P < 0.05) expression of p-eNOS
, NO generation, O
production, BECLIN1, microtubule-associated proteins 1A/1B light chain 3B, autophagy-related gene 3, and lysosomal-associated membrane protein 2A and decreased ( P < 0.05) expression (i.e., enhanced degradation) of the adaptor protein p62/sequestosome-1. These novel findings provide evidence that elevated arterial shear rate associated with functional hyperemia initiates autophagy, activates p-eNOS
, and increases NO and O
generation in primary human ECs. NEW & NOTEWORTHY Previously, our group reported in bovine arterial and human arterial endothelial cells (ECs) that shear stress initiates trafficking of the autophagosome to the lysosome and increases endothelial nitric oxide (NO) synthase phosphorylation at serine 1177, NO generation, and O
production. Here, the translational relevance of these findings is documented. Specifically, functional hyperemia induced by rhythmic handgrip exercise elevates arterial shear rate to an extent that increases indices of autophagy, NO generation, and O
production in primary arterial ECs collected from healthy men.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>30412436</pmid><doi>10.1152/ajpheart.00561.2018</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antibodies Arteries - cytology Arteries - metabolism Arteries - physiology Autophagy Blood pressure Cadherins Cardiac output Cells, Cultured Endothelial cells Endothelial Cells - metabolism Endothelium, Vascular - cytology Endothelium, Vascular - metabolism Exercise Hand Strength Heart rate Humans Hyperemia Male Membrane proteins Microtubule-associated proteins Nitric oxide Nitric Oxide - metabolism Nitric Oxide Synthase Type III - metabolism Nitric-oxide synthase Phagocytosis Phosphorylation Proteins Rapid Report Rhythms Serine Shear rate Shear stress Superoxide |
title | Elevated arterial shear rate increases indexes of endothelial cell autophagy and nitric oxide synthase activation in humans |
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