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Signal transduction by G-proteins, Rho-kinase and protein phosphatase to smooth muscle and non-muscle myosin II
We here review mechanisms that can regulate the activity of myosin II, in smooth muscle and non-muscle cells, by modulating the Ca 2+ sensitivity of myosin regulatory light chain (RLC) phosphorylation. The major mechanism of Ca 2+ sensitization of smooth muscle contraction and non-muscle cell motili...
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Published in: | The Journal of physiology 2000-01, Vol.522 (2), p.177-185 |
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description | We here review mechanisms that can regulate the activity of myosin II, in smooth muscle and non-muscle cells, by modulating
the Ca 2+ sensitivity of myosin regulatory light chain (RLC) phosphorylation. The major mechanism of Ca 2+ sensitization of smooth muscle contraction and non-muscle cell motility is through inhibition of the smooth muscle myosin
phosphatase (MLCP) that dephosphorylates the RLC in smooth muscle and non-muscle. The active, GTP-bound form of the small
GTPase RhoA activates a serine/threonine kinase, Rho-kinase, that phosphorylates the regulatory subunit of MLCP and inhibits
phosphatase activity. G-protein-coupled release of arachidonic acid may also contribute to inhibition of MLCP acting, at least
in part, through the Rho/Rho-kinase pathway. Protein kinase C(s) activated by phorbol esters and diacylglycerol can also inhibit
MLCP by phosphorylating and thereby activating CPI-17, an inhibitor of its catalytic subunit; this mechanism is independent
of the Rho/Rho-kinase pathway and plays only a minor, transient role in the G-protein-coupled mechanism of Ca 2+ sensitization. Ca 2+ sensitization by the Rho/Rho-kinase pathway contributes to the tonic phase of agonist-induced contraction in smooth muscle,
and abnormally increased activation of myosin II by this mechanism is thought to play a role in diseases such as high blood
pressure and cancer cell metastasis. |
doi_str_mv | 10.1111/j.1469-7793.2000.t01-2-00177.x |
format | article |
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the Ca 2+ sensitivity of myosin regulatory light chain (RLC) phosphorylation. The major mechanism of Ca 2+ sensitization of smooth muscle contraction and non-muscle cell motility is through inhibition of the smooth muscle myosin
phosphatase (MLCP) that dephosphorylates the RLC in smooth muscle and non-muscle. The active, GTP-bound form of the small
GTPase RhoA activates a serine/threonine kinase, Rho-kinase, that phosphorylates the regulatory subunit of MLCP and inhibits
phosphatase activity. G-protein-coupled release of arachidonic acid may also contribute to inhibition of MLCP acting, at least
in part, through the Rho/Rho-kinase pathway. Protein kinase C(s) activated by phorbol esters and diacylglycerol can also inhibit
MLCP by phosphorylating and thereby activating CPI-17, an inhibitor of its catalytic subunit; this mechanism is independent
of the Rho/Rho-kinase pathway and plays only a minor, transient role in the G-protein-coupled mechanism of Ca 2+ sensitization. Ca 2+ sensitization by the Rho/Rho-kinase pathway contributes to the tonic phase of agonist-induced contraction in smooth muscle,
and abnormally increased activation of myosin II by this mechanism is thought to play a role in diseases such as high blood
pressure and cancer cell metastasis.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1111/j.1469-7793.2000.t01-2-00177.x</identifier><identifier>PMID: 10639096</identifier><language>eng</language><publisher>Oxford, UK: The Physiological Society</publisher><subject>Animals ; GTP-Binding Proteins - physiology ; Humans ; Intracellular Signaling Peptides and Proteins ; Muscle, Smooth - enzymology ; Muscle, Smooth - physiology ; Myosins - physiology ; Phosphoprotein Phosphatases - physiology ; Protein Conformation ; Protein-Serine-Threonine Kinases - physiology ; rho-Associated Kinases ; Signal Transduction - physiology ; Topical Review</subject><ispartof>The Journal of physiology, 2000-01, Vol.522 (2), p.177-185</ispartof><rights>2000 The Journal of Physiology © 2000 The Physiological Society</rights><rights>The Physiological Society 2000 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5917-53609451c3b71b273bb44b13567beb6e2c04709fd6cde80c6b7bc4d787f420273</citedby><cites>FETCH-LOGICAL-c5917-53609451c3b71b273bb44b13567beb6e2c04709fd6cde80c6b7bc4d787f420273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2269761/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2269761/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10639096$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Somlyo, Andrew P.</creatorcontrib><creatorcontrib>Somlyo, Avril V.</creatorcontrib><title>Signal transduction by G-proteins, Rho-kinase and protein phosphatase to smooth muscle and non-muscle myosin II</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>We here review mechanisms that can regulate the activity of myosin II, in smooth muscle and non-muscle cells, by modulating
the Ca 2+ sensitivity of myosin regulatory light chain (RLC) phosphorylation. The major mechanism of Ca 2+ sensitization of smooth muscle contraction and non-muscle cell motility is through inhibition of the smooth muscle myosin
phosphatase (MLCP) that dephosphorylates the RLC in smooth muscle and non-muscle. The active, GTP-bound form of the small
GTPase RhoA activates a serine/threonine kinase, Rho-kinase, that phosphorylates the regulatory subunit of MLCP and inhibits
phosphatase activity. G-protein-coupled release of arachidonic acid may also contribute to inhibition of MLCP acting, at least
in part, through the Rho/Rho-kinase pathway. Protein kinase C(s) activated by phorbol esters and diacylglycerol can also inhibit
MLCP by phosphorylating and thereby activating CPI-17, an inhibitor of its catalytic subunit; this mechanism is independent
of the Rho/Rho-kinase pathway and plays only a minor, transient role in the G-protein-coupled mechanism of Ca 2+ sensitization. Ca 2+ sensitization by the Rho/Rho-kinase pathway contributes to the tonic phase of agonist-induced contraction in smooth muscle,
and abnormally increased activation of myosin II by this mechanism is thought to play a role in diseases such as high blood
pressure and cancer cell metastasis.</description><subject>Animals</subject><subject>GTP-Binding Proteins - physiology</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins</subject><subject>Muscle, Smooth - enzymology</subject><subject>Muscle, Smooth - physiology</subject><subject>Myosins - physiology</subject><subject>Phosphoprotein Phosphatases - physiology</subject><subject>Protein Conformation</subject><subject>Protein-Serine-Threonine Kinases - physiology</subject><subject>rho-Associated Kinases</subject><subject>Signal Transduction - physiology</subject><subject>Topical Review</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqVkcFu1DAQhi0EotvCK6CcygUH20ns9QUJKloWVQLR9jyKHe_GS2KncUKbt8chq7Ycm4tjzz_f2PoQOqUkpfH7uE9pziUWQmYpI4SkA6GYYUKoEOn9C7R6KL9EK0IYw5ko6BE6DmEfQxmR8jU6ooRnkki-Qv7K7lzZJENfulCNerDeJWpKLnDX-8FYFz4kv2qPf1tXBpOUrkoOhaSrfejqcpjPB5-E1vuhTtox6GYJOu_wYdtOPsSWzeYNerUtm2DeHtYTdHP-9frsG778cbE5-3yJdSGpwEXGicwLqjMlqGIiUyrPFc0KLpRR3DBNckHktuK6MmuiuRJK55VYi23OSMyfoE8LtxtVayptXHxhA11v27KfwJcW_q84W8PO_wHGuBScRsDpAdD729GEAVobtGma0hk_BhBkHSfl68dJuvch9Gb7MIQSmJ3BHmYpMEuB2RlEZ8DgnzO4j4B3T6_6pH2RFANflsCdbcz0TDxcf_8ZfyLk_QKp7a6-s72Brp6C9cFra4YJCsZi05z8C3K6uE4</recordid><startdate>20000115</startdate><enddate>20000115</enddate><creator>Somlyo, Andrew P.</creator><creator>Somlyo, Avril V.</creator><general>The Physiological Society</general><general>Blackwell Science Ltd</general><general>Blackwell Science Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20000115</creationdate><title>Signal transduction by G-proteins, Rho-kinase and protein phosphatase to smooth muscle and non-muscle myosin II</title><author>Somlyo, Andrew P. ; Somlyo, Avril V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5917-53609451c3b71b273bb44b13567beb6e2c04709fd6cde80c6b7bc4d787f420273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>GTP-Binding Proteins - physiology</topic><topic>Humans</topic><topic>Intracellular Signaling Peptides and Proteins</topic><topic>Muscle, Smooth - enzymology</topic><topic>Muscle, Smooth - physiology</topic><topic>Myosins - physiology</topic><topic>Phosphoprotein Phosphatases - physiology</topic><topic>Protein Conformation</topic><topic>Protein-Serine-Threonine Kinases - physiology</topic><topic>rho-Associated Kinases</topic><topic>Signal Transduction - physiology</topic><topic>Topical Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Somlyo, Andrew P.</creatorcontrib><creatorcontrib>Somlyo, Avril V.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Somlyo, Andrew P.</au><au>Somlyo, Avril V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Signal transduction by G-proteins, Rho-kinase and protein phosphatase to smooth muscle and non-muscle myosin II</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2000-01-15</date><risdate>2000</risdate><volume>522</volume><issue>2</issue><spage>177</spage><epage>185</epage><pages>177-185</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>We here review mechanisms that can regulate the activity of myosin II, in smooth muscle and non-muscle cells, by modulating
the Ca 2+ sensitivity of myosin regulatory light chain (RLC) phosphorylation. The major mechanism of Ca 2+ sensitization of smooth muscle contraction and non-muscle cell motility is through inhibition of the smooth muscle myosin
phosphatase (MLCP) that dephosphorylates the RLC in smooth muscle and non-muscle. The active, GTP-bound form of the small
GTPase RhoA activates a serine/threonine kinase, Rho-kinase, that phosphorylates the regulatory subunit of MLCP and inhibits
phosphatase activity. G-protein-coupled release of arachidonic acid may also contribute to inhibition of MLCP acting, at least
in part, through the Rho/Rho-kinase pathway. Protein kinase C(s) activated by phorbol esters and diacylglycerol can also inhibit
MLCP by phosphorylating and thereby activating CPI-17, an inhibitor of its catalytic subunit; this mechanism is independent
of the Rho/Rho-kinase pathway and plays only a minor, transient role in the G-protein-coupled mechanism of Ca 2+ sensitization. Ca 2+ sensitization by the Rho/Rho-kinase pathway contributes to the tonic phase of agonist-induced contraction in smooth muscle,
and abnormally increased activation of myosin II by this mechanism is thought to play a role in diseases such as high blood
pressure and cancer cell metastasis.</abstract><cop>Oxford, UK</cop><pub>The Physiological Society</pub><pmid>10639096</pmid><doi>10.1111/j.1469-7793.2000.t01-2-00177.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals GTP-Binding Proteins - physiology Humans Intracellular Signaling Peptides and Proteins Muscle, Smooth - enzymology Muscle, Smooth - physiology Myosins - physiology Phosphoprotein Phosphatases - physiology Protein Conformation Protein-Serine-Threonine Kinases - physiology rho-Associated Kinases Signal Transduction - physiology Topical Review |
title | Signal transduction by G-proteins, Rho-kinase and protein phosphatase to smooth muscle and non-muscle myosin II |
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