KCNK1 inhibits osteoclastogenesis by blocking the Ca2+ oscillation and JNK-NFATc1 signaling axis
KCNK1 (K(+) channel, subfamily K, member 1) is a member of the inwardly rectifying K(+) channel family, which drives the membrane potential towards the K(+) balance potential. Here, we investigated its functional relevance during osteoclast differentiation. KCNK1 was significantly induced during ost...
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Veröffentlicht in: | Journal of cell science 2015-09, Vol.128 (18), p.3411-3419 |
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container_title | Journal of cell science |
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creator | Yeon, Jeong-Tae Kim, Kwang-Jin Chun, Sang Woo Lee, Hae In Lim, Ji Yeon Son, Young-Jin Kim, Seong Hwan Choi, Sik-Won |
description | KCNK1 (K(+) channel, subfamily K, member 1) is a member of the inwardly rectifying K(+) channel family, which drives the membrane potential towards the K(+) balance potential. Here, we investigated its functional relevance during osteoclast differentiation. KCNK1 was significantly induced during osteoclast differentiation, but its functional overexpression significantly inhibited osteoclast differentiation induced by RANKL (also known as TNFSF11), which was accompanied by the attenuation of the RANKL-induced Ca(2+) oscillation, JNK activation and NFATc1 expression. In contrast, KCNK1 knockdown enhanced the RANKL-induced osteoclast differentiation, JNK activation and NFATc1 expression. In conclusion, we suggest that KCNK1 is a negative regulator of osteoclast differentiation; the increase of K(+) influx by its functional blockade might inhibit osteoclast differentiation by inhibiting Ca(2+) oscillation and the JNK-NFATc1 signaling axis. Together with the increased attention on the pharmacological possibilities of using channel inhibition in the treatment of osteoclast-related disorders, further understanding of the functional roles and mechanisms of K(+) channels underlying osteoclast-related diseases could be helpful in developing relevant therapeutic strategies. |
doi_str_mv | 10.1242/jcs.170738 |
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Here, we investigated its functional relevance during osteoclast differentiation. KCNK1 was significantly induced during osteoclast differentiation, but its functional overexpression significantly inhibited osteoclast differentiation induced by RANKL (also known as TNFSF11), which was accompanied by the attenuation of the RANKL-induced Ca(2+) oscillation, JNK activation and NFATc1 expression. In contrast, KCNK1 knockdown enhanced the RANKL-induced osteoclast differentiation, JNK activation and NFATc1 expression. In conclusion, we suggest that KCNK1 is a negative regulator of osteoclast differentiation; the increase of K(+) influx by its functional blockade might inhibit osteoclast differentiation by inhibiting Ca(2+) oscillation and the JNK-NFATc1 signaling axis. Together with the increased attention on the pharmacological possibilities of using channel inhibition in the treatment of osteoclast-related disorders, further understanding of the functional roles and mechanisms of K(+) channels underlying osteoclast-related diseases could be helpful in developing relevant therapeutic strategies.</description><identifier>ISSN: 0021-9533</identifier><identifier>EISSN: 1477-9137</identifier><identifier>DOI: 10.1242/jcs.170738</identifier><identifier>PMID: 26208638</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Calcium Signaling ; Cell Differentiation ; Cells, Cultured ; Down-Regulation ; Gene Knockdown Techniques ; MAP Kinase Signaling System ; Mice ; NFATC Transcription Factors - metabolism ; Osteoclasts - cytology ; Osteoclasts - metabolism ; Potassium Channels, Tandem Pore Domain - genetics ; Potassium Channels, Tandem Pore Domain - metabolism ; RANK Ligand - metabolism</subject><ispartof>Journal of cell science, 2015-09, Vol.128 (18), p.3411-3419</ispartof><rights>2015. 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Here, we investigated its functional relevance during osteoclast differentiation. KCNK1 was significantly induced during osteoclast differentiation, but its functional overexpression significantly inhibited osteoclast differentiation induced by RANKL (also known as TNFSF11), which was accompanied by the attenuation of the RANKL-induced Ca(2+) oscillation, JNK activation and NFATc1 expression. In contrast, KCNK1 knockdown enhanced the RANKL-induced osteoclast differentiation, JNK activation and NFATc1 expression. In conclusion, we suggest that KCNK1 is a negative regulator of osteoclast differentiation; the increase of K(+) influx by its functional blockade might inhibit osteoclast differentiation by inhibiting Ca(2+) oscillation and the JNK-NFATc1 signaling axis. Together with the increased attention on the pharmacological possibilities of using channel inhibition in the treatment of osteoclast-related disorders, further understanding of the functional roles and mechanisms of K(+) channels underlying osteoclast-related diseases could be helpful in developing relevant therapeutic strategies.</description><subject>Animals</subject><subject>Calcium Signaling</subject><subject>Cell Differentiation</subject><subject>Cells, Cultured</subject><subject>Down-Regulation</subject><subject>Gene Knockdown Techniques</subject><subject>MAP Kinase Signaling System</subject><subject>Mice</subject><subject>NFATC Transcription Factors - metabolism</subject><subject>Osteoclasts - cytology</subject><subject>Osteoclasts - metabolism</subject><subject>Potassium Channels, Tandem Pore Domain - genetics</subject><subject>Potassium Channels, Tandem Pore Domain - metabolism</subject><subject>RANK Ligand - metabolism</subject><issn>0021-9533</issn><issn>1477-9137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EoqWw8AOQRySU4jsnsT1WEeWjVVnKHGzHaV3SpNSJRP89QZSZ6Zbn3ve5I-Qa2BgwxvuNDWMQTHB5QoYQCxEp4OKUDBlDiFTC-YBchLBhjAlU4pwMMEUmUy6H5H2WLWZAfb32xreBNqF1ja10aJuVq13wgZoDNVVjP3y9ou3a0UzjXc9ZX1W69U1NdV3Ql8UsWkwnSws0-FWtqx9af_lwSc5KXQV3dZwj8jZ9WGZP0fz18TmbzKMdiLiNeBIzjVhw2Ru6FDVjqUYtAbFkxijF0VojBVgopRNJnJSKCVUk_Sk2lYyPyO1v7m7ffHYutPnWB-t6x9o1XchBAvQbHPj_qACeoEz70hG5OaKd2boi3-39Vu8P-d8D-TfN9W7l</recordid><startdate>20150915</startdate><enddate>20150915</enddate><creator>Yeon, Jeong-Tae</creator><creator>Kim, Kwang-Jin</creator><creator>Chun, Sang Woo</creator><creator>Lee, Hae In</creator><creator>Lim, Ji Yeon</creator><creator>Son, Young-Jin</creator><creator>Kim, Seong Hwan</creator><creator>Choi, Sik-Won</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7QP</scope></search><sort><creationdate>20150915</creationdate><title>KCNK1 inhibits osteoclastogenesis by blocking the Ca2+ oscillation and JNK-NFATc1 signaling axis</title><author>Yeon, Jeong-Tae ; Kim, Kwang-Jin ; Chun, Sang Woo ; Lee, Hae In ; Lim, Ji Yeon ; Son, Young-Jin ; Kim, Seong Hwan ; Choi, Sik-Won</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p174t-3540a22d38297e62a006a2a8122f0bb9932ccb871c1f8e7545f9079d5262c6803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Calcium Signaling</topic><topic>Cell Differentiation</topic><topic>Cells, Cultured</topic><topic>Down-Regulation</topic><topic>Gene Knockdown Techniques</topic><topic>MAP Kinase Signaling System</topic><topic>Mice</topic><topic>NFATC Transcription Factors - metabolism</topic><topic>Osteoclasts - cytology</topic><topic>Osteoclasts - metabolism</topic><topic>Potassium Channels, Tandem Pore Domain - genetics</topic><topic>Potassium Channels, Tandem Pore Domain - metabolism</topic><topic>RANK Ligand - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yeon, Jeong-Tae</creatorcontrib><creatorcontrib>Kim, Kwang-Jin</creatorcontrib><creatorcontrib>Chun, Sang Woo</creatorcontrib><creatorcontrib>Lee, Hae In</creatorcontrib><creatorcontrib>Lim, Ji Yeon</creatorcontrib><creatorcontrib>Son, Young-Jin</creatorcontrib><creatorcontrib>Kim, Seong Hwan</creatorcontrib><creatorcontrib>Choi, Sik-Won</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Calcium & Calcified Tissue Abstracts</collection><jtitle>Journal of cell science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yeon, Jeong-Tae</au><au>Kim, Kwang-Jin</au><au>Chun, Sang Woo</au><au>Lee, Hae In</au><au>Lim, Ji Yeon</au><au>Son, Young-Jin</au><au>Kim, Seong Hwan</au><au>Choi, Sik-Won</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>KCNK1 inhibits osteoclastogenesis by blocking the Ca2+ oscillation and JNK-NFATc1 signaling axis</atitle><jtitle>Journal of cell science</jtitle><addtitle>J Cell Sci</addtitle><date>2015-09-15</date><risdate>2015</risdate><volume>128</volume><issue>18</issue><spage>3411</spage><epage>3419</epage><pages>3411-3419</pages><issn>0021-9533</issn><eissn>1477-9137</eissn><abstract>KCNK1 (K(+) channel, subfamily K, member 1) is a member of the inwardly rectifying K(+) channel family, which drives the membrane potential towards the K(+) balance potential. Here, we investigated its functional relevance during osteoclast differentiation. KCNK1 was significantly induced during osteoclast differentiation, but its functional overexpression significantly inhibited osteoclast differentiation induced by RANKL (also known as TNFSF11), which was accompanied by the attenuation of the RANKL-induced Ca(2+) oscillation, JNK activation and NFATc1 expression. In contrast, KCNK1 knockdown enhanced the RANKL-induced osteoclast differentiation, JNK activation and NFATc1 expression. In conclusion, we suggest that KCNK1 is a negative regulator of osteoclast differentiation; the increase of K(+) influx by its functional blockade might inhibit osteoclast differentiation by inhibiting Ca(2+) oscillation and the JNK-NFATc1 signaling axis. Together with the increased attention on the pharmacological possibilities of using channel inhibition in the treatment of osteoclast-related disorders, further understanding of the functional roles and mechanisms of K(+) channels underlying osteoclast-related diseases could be helpful in developing relevant therapeutic strategies.</abstract><cop>England</cop><pmid>26208638</pmid><doi>10.1242/jcs.170738</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Calcium Signaling Cell Differentiation Cells, Cultured Down-Regulation Gene Knockdown Techniques MAP Kinase Signaling System Mice NFATC Transcription Factors - metabolism Osteoclasts - cytology Osteoclasts - metabolism Potassium Channels, Tandem Pore Domain - genetics Potassium Channels, Tandem Pore Domain - metabolism RANK Ligand - metabolism |
title | KCNK1 inhibits osteoclastogenesis by blocking the Ca2+ oscillation and JNK-NFATc1 signaling axis |
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