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
Hauptverfasser: Yeon, Jeong-Tae, Kim, Kwang-Jin, Chun, Sang Woo, Lee, Hae In, Lim, Ji Yeon, Son, Young-Jin, Kim, Seong Hwan, Choi, Sik-Won
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container_end_page 3419
container_issue 18
container_start_page 3411
container_title Journal of cell science
container_volume 128
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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source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection; Company of Biologists
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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