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2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand, induces rapid actin polymerization in HL-60 cells differentiated into macrophage-like cells
Delta9-Tetrahydrocannabinol, a major psychoactive constituent of marijuana, interacts with specific receptors, i.e. the cannabinoid receptors, thereby eliciting a variety of pharmacological responses. To date, two types of cannabinoid receptors have been identified: the CB1 receptor, which is abunda...
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Published in: | Biochemical journal 2005-03, Vol.386 (Pt 3), p.583-589 |
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description | Delta9-Tetrahydrocannabinol, a major psychoactive constituent of marijuana, interacts with specific receptors, i.e. the cannabinoid receptors, thereby eliciting a variety of pharmacological responses. To date, two types of cannabinoid receptors have been identified: the CB1 receptor, which is abundantly expressed in the nervous system, and the CB2 receptor, which is predominantly expressed in the immune system. Previously, we investigated in detail the structure-activity relationship of various cannabinoid receptor ligands and found that 2-AG (2-arachidonoylglycerol) is the most efficacious agonist. We have proposed that 2-AG is the true natural ligand for both the CB1 and CB2 receptors. Despite the potential physiological importance of 2-AG, not much information is available concerning its biological activities towards mammalian tissues and cells. In the present study, we examined the effect of 2-AG on morphology as well as the actin filament system in differentiated HL-60 cells, which express the CB2 receptor. We found that 2-AG induces rapid morphological changes such as the extension of pseudopods. We also found that it provokes a rapid actin polymerization in these cells. Actin polymerization induced by 2-AG was abolished when cells were treated with SR144528, a CB2 receptor antagonist, and pertussis toxin, suggesting that the response was mediated by the CB2 receptor and G(i/o). A phosphoinositide 3-kinase, Rho family small G-proteins and a tyrosine kinase were also suggested to be involved. Reorganization of the actin filament system is known to be indispensable for a variety of cellular events; it is possible that 2-AG plays physiologically essential roles in various inflammatory cells and immune-competent cells by inducing a rapid actin rearrangement. |
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To date, two types of cannabinoid receptors have been identified: the CB1 receptor, which is abundantly expressed in the nervous system, and the CB2 receptor, which is predominantly expressed in the immune system. Previously, we investigated in detail the structure-activity relationship of various cannabinoid receptor ligands and found that 2-AG (2-arachidonoylglycerol) is the most efficacious agonist. We have proposed that 2-AG is the true natural ligand for both the CB1 and CB2 receptors. Despite the potential physiological importance of 2-AG, not much information is available concerning its biological activities towards mammalian tissues and cells. In the present study, we examined the effect of 2-AG on morphology as well as the actin filament system in differentiated HL-60 cells, which express the CB2 receptor. We found that 2-AG induces rapid morphological changes such as the extension of pseudopods. We also found that it provokes a rapid actin polymerization in these cells. Actin polymerization induced by 2-AG was abolished when cells were treated with SR144528, a CB2 receptor antagonist, and pertussis toxin, suggesting that the response was mediated by the CB2 receptor and G(i/o). A phosphoinositide 3-kinase, Rho family small G-proteins and a tyrosine kinase were also suggested to be involved. 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To date, two types of cannabinoid receptors have been identified: the CB1 receptor, which is abundantly expressed in the nervous system, and the CB2 receptor, which is predominantly expressed in the immune system. Previously, we investigated in detail the structure-activity relationship of various cannabinoid receptor ligands and found that 2-AG (2-arachidonoylglycerol) is the most efficacious agonist. We have proposed that 2-AG is the true natural ligand for both the CB1 and CB2 receptors. Despite the potential physiological importance of 2-AG, not much information is available concerning its biological activities towards mammalian tissues and cells. In the present study, we examined the effect of 2-AG on morphology as well as the actin filament system in differentiated HL-60 cells, which express the CB2 receptor. We found that 2-AG induces rapid morphological changes such as the extension of pseudopods. We also found that it provokes a rapid actin polymerization in these cells. Actin polymerization induced by 2-AG was abolished when cells were treated with SR144528, a CB2 receptor antagonist, and pertussis toxin, suggesting that the response was mediated by the CB2 receptor and G(i/o). A phosphoinositide 3-kinase, Rho family small G-proteins and a tyrosine kinase were also suggested to be involved. Reorganization of the actin filament system is known to be indispensable for a variety of cellular events; it is possible that 2-AG plays physiologically essential roles in various inflammatory cells and immune-competent cells by inducing a rapid actin rearrangement.</description><subject>Actins - chemistry</subject><subject>Actins - metabolism</subject><subject>ADP Ribose Transferases - metabolism</subject><subject>ADP Ribose Transferases - pharmacology</subject><subject>Arachidonic Acids - chemistry</subject><subject>Arachidonic Acids - metabolism</subject><subject>Arachidonic Acids - pharmacology</subject><subject>Biopolymers - chemistry</subject><subject>Biopolymers - metabolism</subject><subject>Botulinum Toxins - metabolism</subject><subject>Botulinum Toxins - pharmacology</subject><subject>Cannabinoid Receptor Agonists</subject><subject>Cannabinoid Receptor Antagonists</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Shape - drug effects</subject><subject>Endocannabinoids</subject><subject>Glycerides - chemistry</subject><subject>Glycerides - metabolism</subject><subject>Glycerides - pharmacology</subject><subject>HL-60 Cells</subject><subject>Humans</subject><subject>Ligands</subject><subject>Macrophages - cytology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>Peptides, Cyclic</subject><subject>Protein Structure, Quaternary - drug effects</subject><subject>Receptors, Cannabinoid - metabolism</subject><subject>Time Factors</subject><issn>0264-6021</issn><issn>1470-8728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpVkUFv1DAQhS0Eokvhwg9APnGomuJxnKxzQYIKaNFKXOAczdqTrMGxg51F2v4YfiuudkXh5JHep-c38xh7CeIKhJJv3n-WQiiAtn7EVqDWotJrqR-zlZCtqloh4Yw9y_m7EKCEEk_ZGTSqacu8Yr9lhQnNztkY4sGP_mAoRX_JMXAKNo4U4j5zgyHg1oXoLE9kaF5i4t6NGOwld8HuDWWecC4ymsUFPkd_mCi5O1xcDAXhN5sShRvyPnPrhoEShcXhQraoS-QTmhTnHY5UefeDjuRz9mRAn-nF6T1n3z5--Hp9U22-fLq9frepjBLrpbIChG1qsKAVdAJNB7qzg2lr1LZRdgDRobSdJo1KW1MPNdYdNIDYtXK7rc_Z26PvvN9OZE2JltD3c3ITpkMf0fX_K8Ht-jH-6gFqpde6GLw-GaT4c0956SeX71fAQOWAvSyHb4RUBbw4gmXbnBMNfz8B0d_X2T_UWeBX_8Z6QE_91X8ADXyemg</recordid><startdate>20050315</startdate><enddate>20050315</enddate><creator>Gokoh, Maiko</creator><creator>Kishimoto, Seishi</creator><creator>Oka, Saori</creator><creator>Mori, Masahiro</creator><creator>Waku, Keizo</creator><creator>Ishima, Yoshio</creator><creator>Sugiura, Takayuki</creator><general>Portland Press Ltd</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>7T5</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20050315</creationdate><title>2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand, induces rapid actin polymerization in HL-60 cells differentiated into macrophage-like cells</title><author>Gokoh, Maiko ; Kishimoto, Seishi ; Oka, Saori ; Mori, Masahiro ; Waku, Keizo ; Ishima, Yoshio ; Sugiura, Takayuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-d010d531d184190ac9189dfc63a8d54df109a2d98e8a48dc3f3a39151aa962bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Actins - chemistry</topic><topic>Actins - metabolism</topic><topic>ADP Ribose Transferases - metabolism</topic><topic>ADP Ribose Transferases - pharmacology</topic><topic>Arachidonic Acids - chemistry</topic><topic>Arachidonic Acids - metabolism</topic><topic>Arachidonic Acids - pharmacology</topic><topic>Biopolymers - chemistry</topic><topic>Biopolymers - metabolism</topic><topic>Botulinum Toxins - metabolism</topic><topic>Botulinum Toxins - pharmacology</topic><topic>Cannabinoid Receptor Agonists</topic><topic>Cannabinoid Receptor Antagonists</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Shape - drug effects</topic><topic>Endocannabinoids</topic><topic>Glycerides - chemistry</topic><topic>Glycerides - metabolism</topic><topic>Glycerides - pharmacology</topic><topic>HL-60 Cells</topic><topic>Humans</topic><topic>Ligands</topic><topic>Macrophages - cytology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - metabolism</topic><topic>Peptides, Cyclic</topic><topic>Protein Structure, Quaternary - drug effects</topic><topic>Receptors, Cannabinoid - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gokoh, Maiko</creatorcontrib><creatorcontrib>Kishimoto, Seishi</creatorcontrib><creatorcontrib>Oka, Saori</creatorcontrib><creatorcontrib>Mori, Masahiro</creatorcontrib><creatorcontrib>Waku, Keizo</creatorcontrib><creatorcontrib>Ishima, Yoshio</creatorcontrib><creatorcontrib>Sugiura, Takayuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gokoh, Maiko</au><au>Kishimoto, Seishi</au><au>Oka, Saori</au><au>Mori, Masahiro</au><au>Waku, Keizo</au><au>Ishima, Yoshio</au><au>Sugiura, Takayuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand, induces rapid actin polymerization in HL-60 cells differentiated into macrophage-like cells</atitle><jtitle>Biochemical journal</jtitle><addtitle>Biochem J</addtitle><date>2005-03-15</date><risdate>2005</risdate><volume>386</volume><issue>Pt 3</issue><spage>583</spage><epage>589</epage><pages>583-589</pages><issn>0264-6021</issn><eissn>1470-8728</eissn><abstract>Delta9-Tetrahydrocannabinol, a major psychoactive constituent of marijuana, interacts with specific receptors, i.e. the cannabinoid receptors, thereby eliciting a variety of pharmacological responses. To date, two types of cannabinoid receptors have been identified: the CB1 receptor, which is abundantly expressed in the nervous system, and the CB2 receptor, which is predominantly expressed in the immune system. Previously, we investigated in detail the structure-activity relationship of various cannabinoid receptor ligands and found that 2-AG (2-arachidonoylglycerol) is the most efficacious agonist. We have proposed that 2-AG is the true natural ligand for both the CB1 and CB2 receptors. Despite the potential physiological importance of 2-AG, not much information is available concerning its biological activities towards mammalian tissues and cells. In the present study, we examined the effect of 2-AG on morphology as well as the actin filament system in differentiated HL-60 cells, which express the CB2 receptor. We found that 2-AG induces rapid morphological changes such as the extension of pseudopods. We also found that it provokes a rapid actin polymerization in these cells. Actin polymerization induced by 2-AG was abolished when cells were treated with SR144528, a CB2 receptor antagonist, and pertussis toxin, suggesting that the response was mediated by the CB2 receptor and G(i/o). A phosphoinositide 3-kinase, Rho family small G-proteins and a tyrosine kinase were also suggested to be involved. Reorganization of the actin filament system is known to be indispensable for a variety of cellular events; it is possible that 2-AG plays physiologically essential roles in various inflammatory cells and immune-competent cells by inducing a rapid actin rearrangement.</abstract><cop>England</cop><pub>Portland Press Ltd</pub><pmid>15456404</pmid><doi>10.1042/BJ20041163</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - chemistry Actins - metabolism ADP Ribose Transferases - metabolism ADP Ribose Transferases - pharmacology Arachidonic Acids - chemistry Arachidonic Acids - metabolism Arachidonic Acids - pharmacology Biopolymers - chemistry Biopolymers - metabolism Botulinum Toxins - metabolism Botulinum Toxins - pharmacology Cannabinoid Receptor Agonists Cannabinoid Receptor Antagonists Cell Differentiation - drug effects Cell Shape - drug effects Endocannabinoids Glycerides - chemistry Glycerides - metabolism Glycerides - pharmacology HL-60 Cells Humans Ligands Macrophages - cytology Macrophages - drug effects Macrophages - metabolism Peptides, Cyclic Protein Structure, Quaternary - drug effects Receptors, Cannabinoid - metabolism Time Factors |
title | 2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand, induces rapid actin polymerization in HL-60 cells differentiated into macrophage-like cells |
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