β-Arrestin 1 Couples Thrombin to the Rapid Activation of the Akt Pathway
: In a variety of cell types including chinese hamster embryonic fibroblasts (IIC9 cells), α‐thrombin is a potent mitogen. Thrombin irreversibly activates Par 1, a member of the seven membrane‐spanning superfamily of G protein‐coupled receptors (GPCRs). This, in turn, activates several heterotrimeri...
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Veröffentlicht in: | Annals of the New York Academy of Sciences 2002-11, Vol.973 (1), p.138-141 |
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description | : In a variety of cell types including chinese hamster embryonic fibroblasts (IIC9 cells), α‐thrombin is a potent mitogen. Thrombin irreversibly activates Par 1, a member of the seven membrane‐spanning superfamily of G protein‐coupled receptors (GPCRs). This, in turn, activates several heterotrimeric G proteins and induces signaling pathways that are critical for cell cycle reentry and proliferation. In IIC9 cells, α‐thrombin activates the phosphatidylinositol‐3‐OH kinase (PI 3‐Kinase)/Akt pathway, which is essential for G1 cell cycle progression. At present the mechanism for activation and regulation of the PI 3‐kinase/Akt pathway is not fully understood. My preliminary data demonstrates a role for β‐arrestin 1 in the regulation of α‐thrombin‐induced Akt activity. In addition to their importance in receptor down‐regulation, β‐arrestins are now known to scaffold proteins involved in stimulating specific signaling pathways. My preliminary data show that ≺‐thrombin activates a rapid Akt activity in a β‐arrestin 1‐dependent manner in IIC9 cells. |
doi_str_mv | 10.1111/j.1749-6632.2002.tb04622.x |
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Thrombin irreversibly activates Par 1, a member of the seven membrane‐spanning superfamily of G protein‐coupled receptors (GPCRs). This, in turn, activates several heterotrimeric G proteins and induces signaling pathways that are critical for cell cycle reentry and proliferation. In IIC9 cells, α‐thrombin activates the phosphatidylinositol‐3‐OH kinase (PI 3‐Kinase)/Akt pathway, which is essential for G1 cell cycle progression. At present the mechanism for activation and regulation of the PI 3‐kinase/Akt pathway is not fully understood. My preliminary data demonstrates a role for β‐arrestin 1 in the regulation of α‐thrombin‐induced Akt activity. In addition to their importance in receptor down‐regulation, β‐arrestins are now known to scaffold proteins involved in stimulating specific signaling pathways. My preliminary data show that ≺‐thrombin activates a rapid Akt activity in a β‐arrestin 1‐dependent manner in IIC9 cells.</description><subject>Akt pathway</subject><subject>Animals</subject><subject>Arrestins - physiology</subject><subject>beta-Arrestin 1</subject><subject>beta-Arrestins</subject><subject>Cell Line</subject><subject>Humans</subject><subject>Kinetics</subject><subject>MAP Kinase Signaling System - physiology</subject><subject>Protein Transport</subject><subject>Protein-Serine-Threonine Kinases</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Proto-Oncogene Proteins c-akt</subject><subject>Thrombin - physiology</subject><subject>α-thrombin</subject><subject>β-arrestin 1</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkEtOwzAQhi0EouVxBRSxYJcwfjS22aBQQVuEAEEFYmU5iaOmpE2xXWivxUE4EymtYM1sRhr_8431IXSMIcJNnY4jzJkM45iSiACQyKfAYkKixRZq_z5tozYA56GQhLbQnnNjAEwE47uohQkTHdGBNhp8fYaJtcb5chrgoFvPZ5VxwXBk60najHwd-JEJHvSszIMk8-W79mU9DeriZ568-uBe-9GHXh6gnUJXzhxu-j4aXl0Ou_3w5q436CY3YcZAipAaAwXjgsZSUyJTQXKhDRBGMsIxcEZknuoY57kscJFCzCTTAgspgMvU0H10ssbObP02b_6tJqXLTFXpqannTnHCOUigTfBsHcxs7Zw1hZrZcqLtUmFQK49qrFay1EqWWnlUG49q0Swfba7M04nJ_1Y34prA-TrwUVZm-Q-0un1JHjEVDSFcE0rnzeKXoO2rijnlHfV821Pi6eL6EfcvVJd-A_2ykPo</recordid><startdate>200211</startdate><enddate>200211</enddate><creator>GOEL, REEMA</creator><creator>BALDASSARE, JOSEPH J.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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></search><sort><creationdate>200211</creationdate><title>β-Arrestin 1 Couples Thrombin to the Rapid Activation of the Akt Pathway</title><author>GOEL, REEMA ; BALDASSARE, JOSEPH J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4098-3ee0f478369a329b82d8ae0242c27107429dba61dd9f1fb06494a81898079be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Akt pathway</topic><topic>Animals</topic><topic>Arrestins - physiology</topic><topic>beta-Arrestin 1</topic><topic>beta-Arrestins</topic><topic>Cell Line</topic><topic>Humans</topic><topic>Kinetics</topic><topic>MAP Kinase Signaling System - physiology</topic><topic>Protein Transport</topic><topic>Protein-Serine-Threonine Kinases</topic><topic>Protein-Tyrosine Kinases - metabolism</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Proto-Oncogene Proteins c-akt</topic><topic>Thrombin - physiology</topic><topic>α-thrombin</topic><topic>β-arrestin 1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GOEL, REEMA</creatorcontrib><creatorcontrib>BALDASSARE, JOSEPH J.</creatorcontrib><collection>Istex</collection><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><jtitle>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GOEL, REEMA</au><au>BALDASSARE, JOSEPH J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>β-Arrestin 1 Couples Thrombin to the Rapid Activation of the Akt Pathway</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>2002-11</date><risdate>2002</risdate><volume>973</volume><issue>1</issue><spage>138</spage><epage>141</epage><pages>138-141</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><abstract>: In a variety of cell types including chinese hamster embryonic fibroblasts (IIC9 cells), α‐thrombin is a potent mitogen. Thrombin irreversibly activates Par 1, a member of the seven membrane‐spanning superfamily of G protein‐coupled receptors (GPCRs). This, in turn, activates several heterotrimeric G proteins and induces signaling pathways that are critical for cell cycle reentry and proliferation. In IIC9 cells, α‐thrombin activates the phosphatidylinositol‐3‐OH kinase (PI 3‐Kinase)/Akt pathway, which is essential for G1 cell cycle progression. At present the mechanism for activation and regulation of the PI 3‐kinase/Akt pathway is not fully understood. My preliminary data demonstrates a role for β‐arrestin 1 in the regulation of α‐thrombin‐induced Akt activity. In addition to their importance in receptor down‐regulation, β‐arrestins are now known to scaffold proteins involved in stimulating specific signaling pathways. My preliminary data show that ≺‐thrombin activates a rapid Akt activity in a β‐arrestin 1‐dependent manner in IIC9 cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12485850</pmid><doi>10.1111/j.1749-6632.2002.tb04622.x</doi><tpages>4</tpages></addata></record> |
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subjects | Akt pathway Animals Arrestins - physiology beta-Arrestin 1 beta-Arrestins Cell Line Humans Kinetics MAP Kinase Signaling System - physiology Protein Transport Protein-Serine-Threonine Kinases Protein-Tyrosine Kinases - metabolism Proto-Oncogene Proteins - metabolism Proto-Oncogene Proteins c-akt Thrombin - physiology α-thrombin β-arrestin 1 |
title | β-Arrestin 1 Couples Thrombin to the Rapid Activation of the Akt Pathway |
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