Loading…
Arginase II activity regulates cytosolic Ca 2+ level in a p32-dependent manner that contributes to Ca 2+ -dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells
Although arginase II (ArgII) is abundant in mitochondria, Ca -accumulating organelles, the relationship between ArgII activity and Ca translocation into mitochondria and the regulation of cytosolic Ca signaling are completely unknown. We investigated the effects of ArgII activity on mitochondrial Ca...
Saved in:
Published in: | Experimental & molecular medicine 2019-06, Vol.51 (6), p.1 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 6 |
container_start_page | 1 |
container_title | Experimental & molecular medicine |
container_volume | 51 |
creator | Koo, Bon-Hyeock Hong, Dongeui Hong, Hyeon Don Lim, Hyun Kyo Hoe, Kwang Lae Won, Moo-Ho Kim, Young Myeong Berkowitz, Dan E Ryoo, Sungwoo |
description | Although arginase II (ArgII) is abundant in mitochondria, Ca
-accumulating organelles, the relationship between ArgII activity and Ca
translocation into mitochondria and the regulation of cytosolic Ca
signaling are completely unknown. We investigated the effects of ArgII activity on mitochondrial Ca
uptake through mitochondrial p32 protein (p32m) and on CaMKII-dependent vascular smooth muscle cell (VSMC) contraction. Native low-density lipoprotein stimulation induced an increase in [Ca
]m as measured by CoCl
-quenched calcein-AM fluorescence, which was prevented by Arg inhibition in hAoSMCs and reduced in mAoSMCs from ArgII
mice. Conversely, [Ca
]c analyzed with Fluo-4 AM was increased by Arg inhibition and ArgII gene knockout. The increased [Ca
]c resulted in CaMKII and MLC 20 phosphorylation, which was associated with enhanced vasoconstriction activity to phenylephrine (PE) in the vascular tension assay. Cy5-tagged siRNA against mitochondrial p32 mRNA (sip32m) abolished mitochondrial Ca
uptake and induced activation of CaMKII. Spermine, a polyamine, induced mitochondrial Ca
uptake and dephosphorylation of CaMKII and was completely inhibited by sip32m incubation. In mAoSMCs from ApoE-null mice fed a high-cholesterol diet (ApoE
+HCD), Arg activity was increased, and spermine concentration was higher than that of wild-type mice. Furthermore, [Ca
]m and p32m levels were elevated, and CaMKII phosphorylation was reduced in mAoSMCs from ApoE
+HCD. In vascular tension experiments, an attenuated response to vasoconstrictors in de-endothelialized aorta from ApoE
+HCD was recovered by incubation of sip32m. ArgII activity-dependent production of spermine augments Ca
transition from the cytosol to the mitochondria in a p32m-dependent manner and regulates CaMKII-dependent constriction in VSMCs. |
doi_str_mv | 10.1038/s12276-019-0262-y |
format | article |
fullrecord | <record><control><sourceid>pubmed</sourceid><recordid>TN_cdi_pubmed_primary_31155612</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>31155612</sourcerecordid><originalsourceid>FETCH-pubmed_primary_311556123</originalsourceid><addsrcrecordid>eNqFkMtOwzAQRS0kRMvjA9ig2SOD7aQpXaIK1O7ZV64ztEZ-yeME5Sf5JhJUJHasZhbnPnQZu5XiQYrq6ZGkUsuGC7niQjWKD2dsrsRK8aaW1YxdEn0IoRb1sr5gs0rKxaKRas6-nvPBBk0I2y1oU2xvywAZD53TBQnMUCJFZw2sNah7cNijAxtAQ6oUbzFhaDEU8DoEzFCOuoCJoWS77yaDEk_KP2yvKY4MjdCYGMPkF_SYjeDi5wgGmlo4m2LKsaANnIr1P5XaSW3GNwP5GMsRfEfGIRh0jq7Z-bt2hDene8XuXl_e1hueur3Hdpey9ToPu98Bqn-BbxFDcJE</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Arginase II activity regulates cytosolic Ca 2+ level in a p32-dependent manner that contributes to Ca 2+ -dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells</title><source>Publicly Available Content Database</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Koo, Bon-Hyeock ; Hong, Dongeui ; Hong, Hyeon Don ; Lim, Hyun Kyo ; Hoe, Kwang Lae ; Won, Moo-Ho ; Kim, Young Myeong ; Berkowitz, Dan E ; Ryoo, Sungwoo</creator><creatorcontrib>Koo, Bon-Hyeock ; Hong, Dongeui ; Hong, Hyeon Don ; Lim, Hyun Kyo ; Hoe, Kwang Lae ; Won, Moo-Ho ; Kim, Young Myeong ; Berkowitz, Dan E ; Ryoo, Sungwoo</creatorcontrib><description>Although arginase II (ArgII) is abundant in mitochondria, Ca
-accumulating organelles, the relationship between ArgII activity and Ca
translocation into mitochondria and the regulation of cytosolic Ca
signaling are completely unknown. We investigated the effects of ArgII activity on mitochondrial Ca
uptake through mitochondrial p32 protein (p32m) and on CaMKII-dependent vascular smooth muscle cell (VSMC) contraction. Native low-density lipoprotein stimulation induced an increase in [Ca
]m as measured by CoCl
-quenched calcein-AM fluorescence, which was prevented by Arg inhibition in hAoSMCs and reduced in mAoSMCs from ArgII
mice. Conversely, [Ca
]c analyzed with Fluo-4 AM was increased by Arg inhibition and ArgII gene knockout. The increased [Ca
]c resulted in CaMKII and MLC 20 phosphorylation, which was associated with enhanced vasoconstriction activity to phenylephrine (PE) in the vascular tension assay. Cy5-tagged siRNA against mitochondrial p32 mRNA (sip32m) abolished mitochondrial Ca
uptake and induced activation of CaMKII. Spermine, a polyamine, induced mitochondrial Ca
uptake and dephosphorylation of CaMKII and was completely inhibited by sip32m incubation. In mAoSMCs from ApoE-null mice fed a high-cholesterol diet (ApoE
+HCD), Arg activity was increased, and spermine concentration was higher than that of wild-type mice. Furthermore, [Ca
]m and p32m levels were elevated, and CaMKII phosphorylation was reduced in mAoSMCs from ApoE
+HCD. In vascular tension experiments, an attenuated response to vasoconstrictors in de-endothelialized aorta from ApoE
+HCD was recovered by incubation of sip32m. ArgII activity-dependent production of spermine augments Ca
transition from the cytosol to the mitochondria in a p32m-dependent manner and regulates CaMKII-dependent constriction in VSMCs.</description><identifier>EISSN: 2092-6413</identifier><identifier>DOI: 10.1038/s12276-019-0262-y</identifier><identifier>PMID: 31155612</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Arginase - metabolism ; Carrier Proteins - metabolism ; Cell Line ; Cytosol - metabolism ; Humans ; Lipoproteins, LDL - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Mitochondrial Proteins - metabolism ; Muscle, Smooth, Vascular - cytology ; Muscle, Smooth, Vascular - physiology ; Myocytes, Smooth Muscle - cytology ; Myocytes, Smooth Muscle - metabolism ; Vasoconstriction</subject><ispartof>Experimental & molecular medicine, 2019-06, Vol.51 (6), p.1</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31155612$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koo, Bon-Hyeock</creatorcontrib><creatorcontrib>Hong, Dongeui</creatorcontrib><creatorcontrib>Hong, Hyeon Don</creatorcontrib><creatorcontrib>Lim, Hyun Kyo</creatorcontrib><creatorcontrib>Hoe, Kwang Lae</creatorcontrib><creatorcontrib>Won, Moo-Ho</creatorcontrib><creatorcontrib>Kim, Young Myeong</creatorcontrib><creatorcontrib>Berkowitz, Dan E</creatorcontrib><creatorcontrib>Ryoo, Sungwoo</creatorcontrib><title>Arginase II activity regulates cytosolic Ca 2+ level in a p32-dependent manner that contributes to Ca 2+ -dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells</title><title>Experimental & molecular medicine</title><addtitle>Exp Mol Med</addtitle><description>Although arginase II (ArgII) is abundant in mitochondria, Ca
-accumulating organelles, the relationship between ArgII activity and Ca
translocation into mitochondria and the regulation of cytosolic Ca
signaling are completely unknown. We investigated the effects of ArgII activity on mitochondrial Ca
uptake through mitochondrial p32 protein (p32m) and on CaMKII-dependent vascular smooth muscle cell (VSMC) contraction. Native low-density lipoprotein stimulation induced an increase in [Ca
]m as measured by CoCl
-quenched calcein-AM fluorescence, which was prevented by Arg inhibition in hAoSMCs and reduced in mAoSMCs from ArgII
mice. Conversely, [Ca
]c analyzed with Fluo-4 AM was increased by Arg inhibition and ArgII gene knockout. The increased [Ca
]c resulted in CaMKII and MLC 20 phosphorylation, which was associated with enhanced vasoconstriction activity to phenylephrine (PE) in the vascular tension assay. Cy5-tagged siRNA against mitochondrial p32 mRNA (sip32m) abolished mitochondrial Ca
uptake and induced activation of CaMKII. Spermine, a polyamine, induced mitochondrial Ca
uptake and dephosphorylation of CaMKII and was completely inhibited by sip32m incubation. In mAoSMCs from ApoE-null mice fed a high-cholesterol diet (ApoE
+HCD), Arg activity was increased, and spermine concentration was higher than that of wild-type mice. Furthermore, [Ca
]m and p32m levels were elevated, and CaMKII phosphorylation was reduced in mAoSMCs from ApoE
+HCD. In vascular tension experiments, an attenuated response to vasoconstrictors in de-endothelialized aorta from ApoE
+HCD was recovered by incubation of sip32m. ArgII activity-dependent production of spermine augments Ca
transition from the cytosol to the mitochondria in a p32m-dependent manner and regulates CaMKII-dependent constriction in VSMCs.</description><subject>Animals</subject><subject>Arginase - metabolism</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell Line</subject><subject>Cytosol - metabolism</subject><subject>Humans</subject><subject>Lipoproteins, LDL - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitochondrial Proteins - metabolism</subject><subject>Muscle, Smooth, Vascular - cytology</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Myocytes, Smooth Muscle - cytology</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Vasoconstriction</subject><issn>2092-6413</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0kRMvjA9ig2SOD7aQpXaIK1O7ZV64ztEZ-yeME5Sf5JhJUJHasZhbnPnQZu5XiQYrq6ZGkUsuGC7niQjWKD2dsrsRK8aaW1YxdEn0IoRb1sr5gs0rKxaKRas6-nvPBBk0I2y1oU2xvywAZD53TBQnMUCJFZw2sNah7cNijAxtAQ6oUbzFhaDEU8DoEzFCOuoCJoWS77yaDEk_KP2yvKY4MjdCYGMPkF_SYjeDi5wgGmlo4m2LKsaANnIr1P5XaSW3GNwP5GMsRfEfGIRh0jq7Z-bt2hDene8XuXl_e1hueur3Hdpey9ToPu98Bqn-BbxFDcJE</recordid><startdate>20190603</startdate><enddate>20190603</enddate><creator>Koo, Bon-Hyeock</creator><creator>Hong, Dongeui</creator><creator>Hong, Hyeon Don</creator><creator>Lim, Hyun Kyo</creator><creator>Hoe, Kwang Lae</creator><creator>Won, Moo-Ho</creator><creator>Kim, Young Myeong</creator><creator>Berkowitz, Dan E</creator><creator>Ryoo, Sungwoo</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20190603</creationdate><title>Arginase II activity regulates cytosolic Ca 2+ level in a p32-dependent manner that contributes to Ca 2+ -dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells</title><author>Koo, Bon-Hyeock ; Hong, Dongeui ; Hong, Hyeon Don ; Lim, Hyun Kyo ; Hoe, Kwang Lae ; Won, Moo-Ho ; Kim, Young Myeong ; Berkowitz, Dan E ; Ryoo, Sungwoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_311556123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Arginase - metabolism</topic><topic>Carrier Proteins - metabolism</topic><topic>Cell Line</topic><topic>Cytosol - metabolism</topic><topic>Humans</topic><topic>Lipoproteins, LDL - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mitochondrial Proteins - metabolism</topic><topic>Muscle, Smooth, Vascular - cytology</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Myocytes, Smooth Muscle - cytology</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Vasoconstriction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koo, Bon-Hyeock</creatorcontrib><creatorcontrib>Hong, Dongeui</creatorcontrib><creatorcontrib>Hong, Hyeon Don</creatorcontrib><creatorcontrib>Lim, Hyun Kyo</creatorcontrib><creatorcontrib>Hoe, Kwang Lae</creatorcontrib><creatorcontrib>Won, Moo-Ho</creatorcontrib><creatorcontrib>Kim, Young Myeong</creatorcontrib><creatorcontrib>Berkowitz, Dan E</creatorcontrib><creatorcontrib>Ryoo, Sungwoo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Experimental & molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koo, Bon-Hyeock</au><au>Hong, Dongeui</au><au>Hong, Hyeon Don</au><au>Lim, Hyun Kyo</au><au>Hoe, Kwang Lae</au><au>Won, Moo-Ho</au><au>Kim, Young Myeong</au><au>Berkowitz, Dan E</au><au>Ryoo, Sungwoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Arginase II activity regulates cytosolic Ca 2+ level in a p32-dependent manner that contributes to Ca 2+ -dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells</atitle><jtitle>Experimental & molecular medicine</jtitle><addtitle>Exp Mol Med</addtitle><date>2019-06-03</date><risdate>2019</risdate><volume>51</volume><issue>6</issue><spage>1</spage><pages>1-</pages><eissn>2092-6413</eissn><abstract>Although arginase II (ArgII) is abundant in mitochondria, Ca
-accumulating organelles, the relationship between ArgII activity and Ca
translocation into mitochondria and the regulation of cytosolic Ca
signaling are completely unknown. We investigated the effects of ArgII activity on mitochondrial Ca
uptake through mitochondrial p32 protein (p32m) and on CaMKII-dependent vascular smooth muscle cell (VSMC) contraction. Native low-density lipoprotein stimulation induced an increase in [Ca
]m as measured by CoCl
-quenched calcein-AM fluorescence, which was prevented by Arg inhibition in hAoSMCs and reduced in mAoSMCs from ArgII
mice. Conversely, [Ca
]c analyzed with Fluo-4 AM was increased by Arg inhibition and ArgII gene knockout. The increased [Ca
]c resulted in CaMKII and MLC 20 phosphorylation, which was associated with enhanced vasoconstriction activity to phenylephrine (PE) in the vascular tension assay. Cy5-tagged siRNA against mitochondrial p32 mRNA (sip32m) abolished mitochondrial Ca
uptake and induced activation of CaMKII. Spermine, a polyamine, induced mitochondrial Ca
uptake and dephosphorylation of CaMKII and was completely inhibited by sip32m incubation. In mAoSMCs from ApoE-null mice fed a high-cholesterol diet (ApoE
+HCD), Arg activity was increased, and spermine concentration was higher than that of wild-type mice. Furthermore, [Ca
]m and p32m levels were elevated, and CaMKII phosphorylation was reduced in mAoSMCs from ApoE
+HCD. In vascular tension experiments, an attenuated response to vasoconstrictors in de-endothelialized aorta from ApoE
+HCD was recovered by incubation of sip32m. ArgII activity-dependent production of spermine augments Ca
transition from the cytosol to the mitochondria in a p32m-dependent manner and regulates CaMKII-dependent constriction in VSMCs.</abstract><cop>United States</cop><pmid>31155612</pmid><doi>10.1038/s12276-019-0262-y</doi></addata></record> |
fulltext | fulltext |
identifier | EISSN: 2092-6413 |
ispartof | Experimental & molecular medicine, 2019-06, Vol.51 (6), p.1 |
issn | 2092-6413 |
language | eng |
recordid | cdi_pubmed_primary_31155612 |
source | Publicly Available Content Database; PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access |
subjects | Animals Arginase - metabolism Carrier Proteins - metabolism Cell Line Cytosol - metabolism Humans Lipoproteins, LDL - metabolism Male Mice Mice, Inbred C57BL Mitochondrial Proteins - metabolism Muscle, Smooth, Vascular - cytology Muscle, Smooth, Vascular - physiology Myocytes, Smooth Muscle - cytology Myocytes, Smooth Muscle - metabolism Vasoconstriction |
title | Arginase II activity regulates cytosolic Ca 2+ level in a p32-dependent manner that contributes to Ca 2+ -dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T03%3A18%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Arginase%20II%20activity%20regulates%20cytosolic%20Ca%202+%20level%20in%20a%20p32-dependent%20manner%20that%20contributes%20to%20Ca%202+%20-dependent%20vasoconstriction%20in%20native%20low-density%20lipoprotein-stimulated%20vascular%20smooth%20muscle%20cells&rft.jtitle=Experimental%20&%20molecular%20medicine&rft.au=Koo,%20Bon-Hyeock&rft.date=2019-06-03&rft.volume=51&rft.issue=6&rft.spage=1&rft.pages=1-&rft.eissn=2092-6413&rft_id=info:doi/10.1038/s12276-019-0262-y&rft_dat=%3Cpubmed%3E31155612%3C/pubmed%3E%3Cgrp_id%3Ecdi_FETCH-pubmed_primary_311556123%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/31155612&rfr_iscdi=true |