Myristoleic acid inhibits osteoclast formation and bone resorption by suppressing the RANKL activation of Src and Pyk2

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• 作者：Jun-Oh Kwon ; Won Jong Jin ; Bongjun Kim ; Hong-Hee Kim ; ^{hhbkim@snu.ac.kr" class="auth_mail" title="E-mail the corresponding author} ; Zang Hee Lee ; ^{zang1959@snu.ac.kr" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Myristoleic acid ; Osteoclast ; Myristoylation ; Src ; Pyk2
• 刊名：European Journal of Pharmacology
• 出版年：2015
• 出版时间：5 December 2015
• 年：2015
• 卷：768
• 期：Complete
• 页码：189-198
• 全文大小：8676 K

文摘

Cytoskeletal changes in osteoclasts such as formation of actin ring is required for bone-resorbing activity. The tyrosine kinase Src is a key player in massive cytoskeletal change of osteoclasts, thereby in bone destruction. In order for Src to be activated, trafficking to the inner plasma membrane via myristoylation is of importance. A previous study reported that myristoleic acid derived from myristic acid, inhibited N-myristoyl-transferase, an essential enzyme for myristoylation process. This prompted us to investigate whether myristoleic acid could affect osteoclastogenesis. Indeed, we observed that myristoleic acid inhibited RANKL-induced osteoclast formation in vitro, especially, at later stages of differentiation. Myristoleic acid attenuated the tyrosine phosphorylation of c-Src and Pyk2, which associates with Src, by RANKL. When myristoleic acid was co-administered with soluble RANKL into mice, RANKL-induced bone loss was substantially prevented. Bone dissection clearly revealed that the number of multinucleated osteoclasts was significantly diminished by myristoleic acid. On the other hand, myristoleic acid treatment had little or no influence on early osteoclast differentiation markers, such as c-Fos and NFATc1, and proteins related to cytoskeletal rearrangement, including DC-STAMP, integrin αv and integrin β3 in vitro. Taken together, our data suggest that myristoleic acid is capable of blocking the formation of large multinucleated osteoclasts and bone resorption likely through suppressing activation of Src and Pyk2.