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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Veröffentlicht in:Experimental cell research 2017-03, Vol.352 (2), p.293-303
Hauptverfasser: Liu, Changyu, Guan, Hanfeng, Cai, Cong, Li, Feng, Xiao, Jun
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Guan, Hanfeng
Cai, Cong
Li, Feng
Xiao, Jun
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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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><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 &amp; 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 &amp; 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. 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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. 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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 &amp; 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 &amp; 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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language eng
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source MEDLINE; Elsevier ScienceDirect Journals Complete
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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