Lipoxin A4 suppresses osteoclastogenesis in RAW264.7 cells and prevents ovariectomy-induced bone loss
Lipoxin A4 (LXA4; 5S, 6R, 15Strihydroxy- 7,9,13-trans-11-eicosatetraenoic acid) is a metabolic product of arachidonic acid under the action of lipoxidase. This lipid molecule plays important roles in several biological functions, especially inflammatory processes. In vivo, LXA4 regulates the inflamm...
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description | Lipoxin A4 (LXA4; 5S, 6R, 15Strihydroxy- 7,9,13-trans-11-eicosatetraenoic acid) is a metabolic product of arachidonic acid under the action of lipoxidase. This lipid molecule plays important roles in several biological functions, especially inflammatory processes. In vivo, LXA4 regulates the inflammatory response through several signaling pathways. Its mechanism suggests that it might have an effect on osteoclastogenesis and bone loss. Using both in vitro and in vivo studies, it was here observed that LXA4 could significantly inhibit the formation and function of osteoclasts and these effects could be blocked by Boc-2, the specific inhibitor of FPR2/ALX (the receptor of LXA4). Meanwhile, LXA4 reduce the amount of ovariectomy-induced bone loss. These protective effects was found to be associated with inhibition of nuclear factor-κB (NF-κB), activator protein-1 (AP-1), PI3K-AKT, and p-38, ERK, and JNK in MAPKs. The expression of the receptor activator of the NF-κB ligand RANKL:osteoprotegerin ratio and serum levels of TNF-α, IL-1β, and IL-6 were decreased by LXA4. Moreover, LXA4 prevented the production of reactive oxygen species (ROS), the expression of osteoclast-specific genes, including tartrate-resistant acid phosphatase (TRAP), cathepsin K (CK), matrix metalloproteinase (MMP)-9, RANK, and osteoclastic related transcription factors of c-Fos, NFATc1 could also be significantly inhibited by LXA4 in a dose-dependent manner. Studies have demonstrated that LXA4 can inhibit the formation and function of osteoclasts through modulation of several pathways both upstream and downstream of RANKL signaling and FPR2/ALX was
involved in the procedures. This shows that LXA4 may be used as a new strategy for the treatment of osteoclast-related diseases.
•Lipoxin A4 can significantly inhibit the formation and function of osteoclasts.•Several pathways both upstream and downstream of RANKL signaling can be inhibit by Lipoxin A4.•Lipoxin A4 can alleviate ovariectomy-induced bone loss effectively. |
doi_str_mv | 10.1016/j.yexcr.2017.02.018 |
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involved in the procedures. This shows that LXA4 may be used as a new strategy for the treatment of osteoclast-related diseases.
•Lipoxin A4 can significantly inhibit the formation and function of osteoclasts.•Several pathways both upstream and downstream of RANKL signaling can be inhibit by Lipoxin A4.•Lipoxin A4 can alleviate ovariectomy-induced bone loss effectively.</description><identifier>ISSN: 0014-4827</identifier><identifier>EISSN: 1090-2422</identifier><identifier>DOI: 10.1016/j.yexcr.2017.02.018</identifier><identifier>PMID: 28209487</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; ACID PHOSPHATASE ; Animals ; ARACHIDONIC ACID ; BIOLOGICAL FUNCTIONS ; Bone Resorption - metabolism ; Bone Resorption - prevention & control ; Cathepsin K - genetics ; Cathepsin K - metabolism ; CATHEPSINS ; Cell Line ; DISEASES ; DOSES ; Female ; GENES ; Humans ; IN VITRO ; IN VIVO ; INFLAMMATION ; INHIBITION ; LIGANDS ; LIPIDS ; Lipoxin A4 ; Lipoxins - pharmacology ; Lipoxins - therapeutic use ; MAP Kinase Signaling System ; MATRICES ; Matrix Metalloproteinase 9 - genetics ; Matrix Metalloproteinase 9 - metabolism ; Mice ; Mice, Inbred C57BL ; MODULATION ; MOLECULES ; NF-kappa B - metabolism ; NF-κB ; Osteoclast ; Osteoclasts - drug effects ; Osteoclasts - metabolism ; Osteoporosis, Postmenopausal - etiology ; Osteoporosis, Postmenopausal - metabolism ; Osteoporosis, Postmenopausal - prevention & control ; Ovariectomy - adverse effects ; OXYGEN ; Phosphatidylinositol 3-Kinases - metabolism ; PHOSPHORUS 38 ; Proto-Oncogene Proteins c-akt - metabolism ; RANK ; RANK Ligand - metabolism ; Reactive Oxygen Species - metabolism ; RECEPTORS ; SIGNALS ; SKELETON ; Tartrate-Resistant Acid Phosphatase - genetics ; Tartrate-Resistant Acid Phosphatase - metabolism ; TARTRATES ; TRANSCRIPTION ; TRANSCRIPTION FACTORS ; TRAPS</subject><ispartof>Experimental cell research, 2017-03, Vol.352 (2), p.293-303</ispartof><rights>2017</rights><rights>Copyright © 2017. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-a8459fd83fdedeadb19c7c22b1272398526d9abf47c5b21e62867fe447e6458e3</citedby><cites>FETCH-LOGICAL-c387t-a8459fd83fdedeadb19c7c22b1272398526d9abf47c5b21e62867fe447e6458e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014482717300630$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28209487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/22649839$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Changyu</creatorcontrib><creatorcontrib>Guan, Hanfeng</creatorcontrib><creatorcontrib>Cai, Cong</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Xiao, Jun</creatorcontrib><title>Lipoxin A4 suppresses osteoclastogenesis in RAW264.7 cells and prevents ovariectomy-induced bone loss</title><title>Experimental cell research</title><addtitle>Exp Cell Res</addtitle><description>Lipoxin A4 (LXA4; 5S, 6R, 15Strihydroxy- 7,9,13-trans-11-eicosatetraenoic acid) is a metabolic product of arachidonic acid under the action of lipoxidase. This lipid molecule plays important roles in several biological functions, especially inflammatory processes. In vivo, LXA4 regulates the inflammatory response through several signaling pathways. Its mechanism suggests that it might have an effect on osteoclastogenesis and bone loss. Using both in vitro and in vivo studies, it was here observed that LXA4 could significantly inhibit the formation and function of osteoclasts and these effects could be blocked by Boc-2, the specific inhibitor of FPR2/ALX (the receptor of LXA4). Meanwhile, LXA4 reduce the amount of ovariectomy-induced bone loss. These protective effects was found to be associated with inhibition of nuclear factor-κB (NF-κB), activator protein-1 (AP-1), PI3K-AKT, and p-38, ERK, and JNK in MAPKs. The expression of the receptor activator of the NF-κB ligand RANKL:osteoprotegerin ratio and serum levels of TNF-α, IL-1β, and IL-6 were decreased by LXA4. Moreover, LXA4 prevented the production of reactive oxygen species (ROS), the expression of osteoclast-specific genes, including tartrate-resistant acid phosphatase (TRAP), cathepsin K (CK), matrix metalloproteinase (MMP)-9, RANK, and osteoclastic related transcription factors of c-Fos, NFATc1 could also be significantly inhibited by LXA4 in a dose-dependent manner. Studies have demonstrated that LXA4 can inhibit the formation and function of osteoclasts through modulation of several pathways both upstream and downstream of RANKL signaling and FPR2/ALX was
involved in the procedures. This shows that LXA4 may be used as a new strategy for the treatment of osteoclast-related diseases.
•Lipoxin A4 can significantly inhibit the formation and function of osteoclasts.•Several pathways both upstream and downstream of RANKL signaling can be inhibit by Lipoxin A4.•Lipoxin A4 can alleviate ovariectomy-induced bone loss effectively.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>ACID PHOSPHATASE</subject><subject>Animals</subject><subject>ARACHIDONIC ACID</subject><subject>BIOLOGICAL FUNCTIONS</subject><subject>Bone Resorption - metabolism</subject><subject>Bone Resorption - prevention & control</subject><subject>Cathepsin K - genetics</subject><subject>Cathepsin K - metabolism</subject><subject>CATHEPSINS</subject><subject>Cell Line</subject><subject>DISEASES</subject><subject>DOSES</subject><subject>Female</subject><subject>GENES</subject><subject>Humans</subject><subject>IN VITRO</subject><subject>IN VIVO</subject><subject>INFLAMMATION</subject><subject>INHIBITION</subject><subject>LIGANDS</subject><subject>LIPIDS</subject><subject>Lipoxin A4</subject><subject>Lipoxins - pharmacology</subject><subject>Lipoxins - therapeutic use</subject><subject>MAP Kinase Signaling System</subject><subject>MATRICES</subject><subject>Matrix Metalloproteinase 9 - genetics</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>MODULATION</subject><subject>MOLECULES</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB</subject><subject>Osteoclast</subject><subject>Osteoclasts - drug effects</subject><subject>Osteoclasts - metabolism</subject><subject>Osteoporosis, Postmenopausal - etiology</subject><subject>Osteoporosis, Postmenopausal - metabolism</subject><subject>Osteoporosis, Postmenopausal - prevention & control</subject><subject>Ovariectomy - adverse effects</subject><subject>OXYGEN</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>PHOSPHORUS 38</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>RANK</subject><subject>RANK Ligand - metabolism</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>RECEPTORS</subject><subject>SIGNALS</subject><subject>SKELETON</subject><subject>Tartrate-Resistant Acid Phosphatase - genetics</subject><subject>Tartrate-Resistant Acid Phosphatase - metabolism</subject><subject>TARTRATES</subject><subject>TRANSCRIPTION</subject><subject>TRANSCRIPTION FACTORS</subject><subject>TRAPS</subject><issn>0014-4827</issn><issn>1090-2422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v1DAQxS0EotvCJ0BCkbhwSbAdx38OHFZVoUgrVapAHC3HnoBXWTvYyar77euwhWNPc_m9mTfvIfSO4IZgwj_tmxM82NRQTESDaYOJfIE2BCtcU0bpS7TBmLCaSSou0GXOe4yxlIS_RhdUUqyYFBsEOz_FBx-qLavyMk0JcoZcxTxDtKPJc_wFAbLPVWHutz8pZ42oLIxjrkxwVREcIcxFcTTJg53j4VT74BYLrupjgGqMOb9BrwYzZnj7NK_Qjy83369v693d12_X211tWynm2kjWqcHJdnDgwLieKCsspT2hgrZKdpQ7ZfqBCdv1lACnkosBGBPAWSehvUIfznuLf6-z9TPY3zaGUIxpWrwr2apCfTxTU4p_FsizPvi8vmQCxCVrIrlSvJOYFLQ9ozaVNxIMekr-YNJJE6zXFvRe_21Bry1oTHVpoajePx1Y-gO4_5p_sRfg8xmAEsbRQ1q9QiiZ-bRaddE_e-ARbSuZ8Q</recordid><startdate>20170315</startdate><enddate>20170315</enddate><creator>Liu, Changyu</creator><creator>Guan, Hanfeng</creator><creator>Cai, Cong</creator><creator>Li, Feng</creator><creator>Xiao, Jun</creator><general>Elsevier 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>OTOTI</scope></search><sort><creationdate>20170315</creationdate><title>Lipoxin A4 suppresses osteoclastogenesis in RAW264.7 cells and prevents ovariectomy-induced bone loss</title><author>Liu, Changyu ; Guan, Hanfeng ; Cai, Cong ; Li, Feng ; Xiao, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-a8459fd83fdedeadb19c7c22b1272398526d9abf47c5b21e62867fe447e6458e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>ACID PHOSPHATASE</topic><topic>Animals</topic><topic>ARACHIDONIC ACID</topic><topic>BIOLOGICAL FUNCTIONS</topic><topic>Bone Resorption - metabolism</topic><topic>Bone Resorption - prevention & control</topic><topic>Cathepsin K - genetics</topic><topic>Cathepsin K - metabolism</topic><topic>CATHEPSINS</topic><topic>Cell Line</topic><topic>DISEASES</topic><topic>DOSES</topic><topic>Female</topic><topic>GENES</topic><topic>Humans</topic><topic>IN VITRO</topic><topic>IN VIVO</topic><topic>INFLAMMATION</topic><topic>INHIBITION</topic><topic>LIGANDS</topic><topic>LIPIDS</topic><topic>Lipoxin A4</topic><topic>Lipoxins - pharmacology</topic><topic>Lipoxins - therapeutic use</topic><topic>MAP Kinase Signaling System</topic><topic>MATRICES</topic><topic>Matrix Metalloproteinase 9 - genetics</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>MODULATION</topic><topic>MOLECULES</topic><topic>NF-kappa B - metabolism</topic><topic>NF-κB</topic><topic>Osteoclast</topic><topic>Osteoclasts - drug effects</topic><topic>Osteoclasts - metabolism</topic><topic>Osteoporosis, Postmenopausal - etiology</topic><topic>Osteoporosis, Postmenopausal - metabolism</topic><topic>Osteoporosis, Postmenopausal - prevention & control</topic><topic>Ovariectomy - adverse effects</topic><topic>OXYGEN</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>PHOSPHORUS 38</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>RANK</topic><topic>RANK Ligand - metabolism</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>RECEPTORS</topic><topic>SIGNALS</topic><topic>SKELETON</topic><topic>Tartrate-Resistant Acid Phosphatase - genetics</topic><topic>Tartrate-Resistant Acid Phosphatase - metabolism</topic><topic>TARTRATES</topic><topic>TRANSCRIPTION</topic><topic>TRANSCRIPTION FACTORS</topic><topic>TRAPS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Changyu</creatorcontrib><creatorcontrib>Guan, Hanfeng</creatorcontrib><creatorcontrib>Cai, Cong</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Xiao, Jun</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>OSTI.GOV</collection><jtitle>Experimental cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Changyu</au><au>Guan, Hanfeng</au><au>Cai, Cong</au><au>Li, Feng</au><au>Xiao, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lipoxin A4 suppresses osteoclastogenesis in RAW264.7 cells and prevents ovariectomy-induced bone loss</atitle><jtitle>Experimental cell research</jtitle><addtitle>Exp Cell Res</addtitle><date>2017-03-15</date><risdate>2017</risdate><volume>352</volume><issue>2</issue><spage>293</spage><epage>303</epage><pages>293-303</pages><issn>0014-4827</issn><eissn>1090-2422</eissn><abstract>Lipoxin A4 (LXA4; 5S, 6R, 15Strihydroxy- 7,9,13-trans-11-eicosatetraenoic acid) is a metabolic product of arachidonic acid under the action of lipoxidase. This lipid molecule plays important roles in several biological functions, especially inflammatory processes. In vivo, LXA4 regulates the inflammatory response through several signaling pathways. Its mechanism suggests that it might have an effect on osteoclastogenesis and bone loss. Using both in vitro and in vivo studies, it was here observed that LXA4 could significantly inhibit the formation and function of osteoclasts and these effects could be blocked by Boc-2, the specific inhibitor of FPR2/ALX (the receptor of LXA4). Meanwhile, LXA4 reduce the amount of ovariectomy-induced bone loss. These protective effects was found to be associated with inhibition of nuclear factor-κB (NF-κB), activator protein-1 (AP-1), PI3K-AKT, and p-38, ERK, and JNK in MAPKs. The expression of the receptor activator of the NF-κB ligand RANKL:osteoprotegerin ratio and serum levels of TNF-α, IL-1β, and IL-6 were decreased by LXA4. Moreover, LXA4 prevented the production of reactive oxygen species (ROS), the expression of osteoclast-specific genes, including tartrate-resistant acid phosphatase (TRAP), cathepsin K (CK), matrix metalloproteinase (MMP)-9, RANK, and osteoclastic related transcription factors of c-Fos, NFATc1 could also be significantly inhibited by LXA4 in a dose-dependent manner. Studies have demonstrated that LXA4 can inhibit the formation and function of osteoclasts through modulation of several pathways both upstream and downstream of RANKL signaling and FPR2/ALX was
involved in the procedures. This shows that LXA4 may be used as a new strategy for the treatment of osteoclast-related diseases.
•Lipoxin A4 can significantly inhibit the formation and function of osteoclasts.•Several pathways both upstream and downstream of RANKL signaling can be inhibit by Lipoxin A4.•Lipoxin A4 can alleviate ovariectomy-induced bone loss effectively.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28209487</pmid><doi>10.1016/j.yexcr.2017.02.018</doi><tpages>11</tpages></addata></record> |
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subjects | 60 APPLIED LIFE SCIENCES ACID PHOSPHATASE Animals ARACHIDONIC ACID BIOLOGICAL FUNCTIONS Bone Resorption - metabolism Bone Resorption - prevention & control Cathepsin K - genetics Cathepsin K - metabolism CATHEPSINS Cell Line DISEASES DOSES Female GENES Humans IN VITRO IN VIVO INFLAMMATION INHIBITION LIGANDS LIPIDS Lipoxin A4 Lipoxins - pharmacology Lipoxins - therapeutic use MAP Kinase Signaling System MATRICES Matrix Metalloproteinase 9 - genetics Matrix Metalloproteinase 9 - metabolism Mice Mice, Inbred C57BL MODULATION MOLECULES NF-kappa B - metabolism NF-κB Osteoclast Osteoclasts - drug effects Osteoclasts - metabolism Osteoporosis, Postmenopausal - etiology Osteoporosis, Postmenopausal - metabolism Osteoporosis, Postmenopausal - prevention & control Ovariectomy - adverse effects OXYGEN Phosphatidylinositol 3-Kinases - metabolism PHOSPHORUS 38 Proto-Oncogene Proteins c-akt - metabolism RANK RANK Ligand - metabolism Reactive Oxygen Species - metabolism RECEPTORS SIGNALS SKELETON Tartrate-Resistant Acid Phosphatase - genetics Tartrate-Resistant Acid Phosphatase - metabolism TARTRATES TRANSCRIPTION TRANSCRIPTION FACTORS TRAPS |
title | Lipoxin A4 suppresses osteoclastogenesis in RAW264.7 cells and prevents ovariectomy-induced bone loss |
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