Journal
BRITISH JOURNAL OF PHARMACOLOGY
Volume 176, Issue 14, Pages 2465-2481Publisher
WILEY
DOI: 10.1111/bph.14674
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Funding
- China Overseas Scholarship Council [201708230063, 201706285111, 201603170211]
- Natural Science Fund of China [81870300]
- Victorian Government's Operational Infrastructure Support Program
- National Health and Medical Research Council [1043026, 1081710]
- National Health and Medical Research Council of Australia [1081710] Funding Source: NHMRC
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Background and Purpose Expression of the pro-fibrotic galectin-3 and the pro-apoptotic BIM is elevated in diseased heart or after beta-adrenoceptor stimulation, but the underlying mechanisms are unclear. This question was addressed in the present study. Experimental Approach Wild-type mice and mice with cardiac transgenic expression of beta(2)-adrenoceptors, mammalian sterile-20 like kinase 1 (Mst1) or dominant-negative Mst1, and non-specific galectin-3 knockout mice were used. Effects of the beta-adrenoceptor agonist isoprenaline or beta-adrenoceptor antagonists were studied. Rat cardiomyoblasts (H9c2) were used for mechanistic exploration. Biochemical assays were performed. Key Results Isoprenaline treatment up-regulated expression of galectin-3 and BIM, and this was inhibited by non-selective or selective beta-adrenoceptor antagonists (by 60-70%). Cardiac expression of galectin-3 and BIM was increased in beta(2)-adrenoceptor transgenic mice. Isoprenaline-induced up-regulation of galectin-3 and BIM was attenuated by Mst1 inactivation, but isoprenaline-induced galectin-3 expression was exaggerated by transgenic Mst1 activation. Pharmacological or genetic activation of beta-adrenoceptors induced Mst1 expression and yes-associated protein (YAP) phosphorylation. YAP hyper-phosphorylation was also evident in Mst1 transgenic hearts with up-regulated expression of galectin-3 (40-fold) and BIM as well as up-regulation of many YAP-target genes by RNA sequencing. In H9c2 cells, isoprenaline induced YAP phosphorylation and expression of galectin-3 and BIM, effects simulated by forskolin but abolished by PKA inhibitors, and YAP knockdown induced expression of galectin-3 and BIM. Conclusions and Implications Stimulation of cardiac beta-adrenoceptors activated the Mst1/Hippo pathway leading to YAP hyper-phosphorylation with enhanced expression of galectin-3 and BIM. This signalling pathway would have therapeutic potential. Linked Articles This article is part of a themed section on Adrenoceptors-New Roles for Old Players. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.14/issuetoc
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