Cardiac-specific TrkB knockout in mice exacerbated heart failure progression and blunted adaptive responses to exercise by decreasing cellular energetics via the Yin Yang 1/PGC-1α pathway.
Myocardial BDNF plays a critical role in regulating cellular energetics in the cardiac stress response through the Yin Yang 1/PGC-1α pathway.
AIMS: Brain-derived neurotrophic factor (BDNF) is markedly decreased in heart failure patients. Both BDNF and its receptor, tropomyosin-related kinase receptor (TrkB), are expressed in cardiomyocytes; however, the role of myocardial BDNF signalling in cardiac pathophysiology is poorly understood. Here, we investigated the role of BDNF/TrkB signalling in cardiac stress response to exercise and pathological stress. METHODS AND RESULTS: We found that myocardial BDNF expression was increased in mice with swimming exercise but decreased in a mouse heart failure model and human failing hearts. Cardiac-specific TrkB knockout (cTrkB KO) mice displayed a blunted adaptive cardiac response to exercise, with attenuated upregulation of transcription factor networks controlling mitochondrial biogenesis/metabolism, including peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC-1α). In response to pathological stress (transaortic constriction, TAC), cTrkB KO mice showed an exacerbated heart failure progression. The downregulation of PGC-1α in cTrkB KO mice exposed to exercise or TAC resulted in decreased cardiac energetics. We further unravelled that BDNF induces PGC-1α upregulation and bioenergetics through a novel signalling pathway, the pleiotropic transcription factor Yin Yang 1. CONCLUSION: Taken together, our findings suggest that myocardial BDNF plays a critical role in regulating cellular energetics in the cardiac stress response.
Yang et al. (Wed,) conducted a other in Heart failure. Cardiac-specific TrkB knockout vs. Wild-type controls was evaluated on Cardiac adaptive response to exercise and pathological stress. Cardiac-specific TrkB knockout in mice exacerbated heart failure progression and blunted adaptive responses to exercise by decreasing cellular energetics via the Yin Yang 1/PGC-1α pathway.