Peroxisome proliferator-activated receptor gamma coactivator 1 alpha protects cardiomyocytes from hypertrophy by suppressing calcineurin-nuclear factor of activated T cells c4 signaling pathway

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• 作者：Xue-Ping Liu^a ; Hui Gao^a ; ^b ; Xiao-Yang Huang^a ; Yan-Fang Chen^c ; Xiao-Jun Feng^a ; Yan-Hong He^a ; Zhuo-Ming Li^a ; ^{lizhm5@mail.sysu.edu.cn" class="auth_mail" title="E-mail the corresponding author} ; Pei-Qing Liu^a ; ^{liupq@mail.sysu.edu.cn" class="auth_mail" title="E-mail the corresponding author}
• 关键词：ANF ; atrial natriuretic factor ; BNP ; brain natriuretic peptide ; co-IP ; coimmunoprecipitation ; EMSA ; electrophoretic mobility shift assays ; 尾-MHC ; myosin heavy chain 尾 ; NFATc4 ; nuclear factor of activated T cells c4 ; PE ; phenylephrine ; PGC-1伪 ; peroxisome proliferator&ndash ; activated receptor gamma coactivator 1 alpha
• 刊名：Translational Research
• 出版年：2015
• 出版时间：November 2015
• 年：2015
• 卷：166
• 期：5
• 页码：459-473.e3
• 全文大小：3186 K

文摘

Peroxisome proliferator–activated receptor gamma coactivator 1 alpha (PGC-1伪) is a crucial coregulator interacting with multiple transcriptional factors in the regulation of cardiac hypertrophy. The present study revealed that PGC-1伪 protected cardiomyocytes from hypertrophy by suppressing calcineurin-nuclear factor of activated T cells c4 (NFATc4) signaling pathway. Overexpression of PGC-1伪 by adenovirus infection prevented the increased protein and messenger RNA expression of NFATc4 in phenylephrine (PE)-treated hypertrophic cardiomyocytes, whereas knockdown of PGC-1伪 by RNA silencing augmented the expression of NFATc4. An interaction between PGC-1伪 and NFATc4 was observed in both the cytoplasm and nucleus of neonatal rat cardiomyocytes. Adenovirus PGC-1伪 prevented the nuclear import of NFATc4 and increased its phosphorylation level of NFATc4, probably through repressing the expression and activity of calcineurin and interfering with the interaction between calcineurin and NFATc4. On the contrary, PGC-1伪 silencing aggravated PE-induced calcineurin activation, NFATc4 dephosphorylation, and nuclear translocation. Moreover, the binding activity and transcription activity of NFATc4 to DNA promoter of brain natriuretic peptide were abrogated by PGC-1伪 overexpression but were enhanced by PGC-1伪 knockdown. The effect of PGC-1伪 on suppressing the calcinuerin-NFATc4 signaling pathway might at least partially contribute to the protective effect of PGC-1伪 on cardiomyocyte hypertrophy. These findings provide novel insights into the role of PGC-1伪 in regulation of cardiac hypertrophy.