Cell Biosci:全反式维甲酸抑制异二聚体骨形态发生蛋白2/7刺激的破骨细胞生成和再吸收活性

2018-09-10 MedSci MedSci原创

骨再生异二聚体骨形态发生蛋白2/7(BMP2/7)增强破骨细胞生成,而全反式视黄酸(ATRA)则会抑制破骨细胞生成。然而,ATRA对生理和/或BMP2/7诱导的破骨细胞生成的影响仍不清楚。在本研究中,我们旨在探究BMP2/7和ATRA联合治疗对破骨细胞生成和再吸收活性的影响。 在鼠前破骨细胞系RAW264.7或小鼠骨髓衍生的巨噬细胞(BMM)培养物中加入全反式视黄酸(1μM)±BMP2/7(

骨再生异二聚体骨形态发生蛋白2/7(BMP2/7)增强破骨细胞生成,而全反式视黄酸(ATRA)则会抑制破骨细胞生成。然而,ATRA对生理和/或BMP2/7诱导的破骨细胞生成的影响仍不清楚。在本研究中,我们旨在探究BMP2/7和ATRA联合治疗对破骨细胞生成和再吸收活性的影响。

在鼠前破骨细胞系RAW264.7或小鼠骨髓衍生的巨噬细胞(BMM)培养物中加入全反式视黄酸(1μM)±BMP2/7(5或50ng / ml)。分析破骨细胞标志物基因表达,破骨细胞生成和再吸收活性。

结果显示,BMP2/7强有力地增强破骨细胞相关基因的表达,破骨细胞的生成和再吸收活性。有趣的是,不论是否存在BMP2/7,ATRA都可完全抑制破骨细胞的形成。视黄酸受体(RAR)的泛拮抗剂和RARα、β或γ的拮抗剂未能逆转ATRA对破骨细胞生成的抑制作用。ATRA科强烈抑制Rank和Nfatc1的表达。全反式视黄酸可能通过RANKL-RANK通路抑制BMP2/7诱导的破骨细胞生成和再吸收活性。

研究认为,ATRA和BMP2/7的联合使用是治疗过度活跃的破骨细胞诱导的骨丢失的新方法,例如炎症诱导的严重骨质疏松症和由癌转移至骨引起的骨丧失。

原始出处:

Wenjuan Bi, Yi Liu, et al., All-trans retinoic-acid inhibits heterodimeric bone morphogenetic protein 2/7-stimulated osteoclastogenesis, and resorption activity. Cell Biosci. 2018; 8: 48.

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    2019-05-19 sunylz
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  5. 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status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1495074, encodeId=7f4214950e4f9, content=<a href='/topic/show?id=3c0b10182102' target=_blank style='color:#2F92EE;'>#骨细胞#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=137, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=101821, encryptionId=3c0b10182102, topicName=骨细胞)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=723c9147696, createdName=jj000004, createdTime=Wed Sep 12 07:59:00 CST 2018, time=2018-09-12, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1588946, encodeId=1af6158894665, content=<a href='/topic/show?id=c4512931961' target=_blank style='color:#2F92EE;'>#全反式维甲酸#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=158, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=29319, encryptionId=c4512931961, topicName=全反式维甲酸)], attachment=null, authenticateStatus=null, 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    2018-12-29 维他命
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