| Vol. 6.33 – 27 September, 2021 |
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| Intimal hyperplasia is a common feature of vascular remodeling disorders. Accumulation of synthetic smooth muscle cell-like cells is the main underlying cause. Researchers investigated the function of PDE10A in smooth muscle cell proliferation and intimal hyperplasia both in vitro and in vivo. [Cardiovascular Research] |
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PUBLICATIONSRanked by the impact factor of the journal |
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| Scientists demonstrated that potentially novel conditional cardiomyocyte–specific miR-150 knock out in mice worsened maladaptive cardiac remodeling after myocardial infarction. [JCI Insight] |
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| Understanding biological mechanisms involved in the long-term alcohol exposure-induced cardiotoxicity is pivotal to the discovery of therapeutic strategies. Cardiomyocytes derived from human pluripotent stem cells were treated with clinically relevant doses of ethanol for various durations up to five weeks. [Stem Cell Reviews and Reports] |
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| Scientists investigated the role of lncRNAs in myocardial ischemia-reperfusion injury. Overexpression of p53 canceled the inhibitory effects of lncRNA-6395 knockdown on cardiomyocyte apoptosis, whereas knockdown of p53 counteracted the apoptotic effects of lncRNA-6395 in cardiomyocytes. [Acta Pharmacologica Sinica] |
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| Investigators defined the underlying role of histone deacetylase 4 (HDAC4) and miR-206 in the pathological process of myocardial ischemia-reperfusion injury (MIRI). Up-regulation of HDAC4 and down-regulation of miR-206 occurred in rat myocardial tissues and cardiomyocytes in MIRI. [Cell Death Discovery] |
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| Researchers showed that methyltransferase-like 3 (METTL3) was downregulated in mice ischemia-reperfusion (I/R) myocardial tissues and hypoxic/re-oxygenated (H/R) cardiomyocytes, and upregulation of METTL3 attenuated I/R and H/R-induced cell apoptosis. [Cell Biology International] |
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| Scientists examined PMI-5011 activation of AMP-activated protein kinase (AMPK) signaling using murine C2C12 muscle cell culture and skeletal muscle tissue. [Biomedicine & Pharmacotherapy] |
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| The authors investigated whether imbalanced mitochondrial dynamics affected mitochondrial function and bioenergetic efficiency in skeletal muscle cells of megaconial congenital muscular dystrophy. [Scientific Reports] |
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| Scientists identified several regulatory regions that control DSTN expression including a SMC-selective enhancer that was activated by the MRTF/SRF, Notch/RBPJ, and SMAD transcription factors. [American Journal of Physiology-Heart and Circulatory Physiology] |
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| Researchers explored the effects of β2-adrenergic stimulation by isoproterenol on vascular smooth muscle cells (VSMC) calcification. Experiments were performed in primary human aortic VSMCs treated with isoproterenol during control or high phosphate conditions. [Pflugers Archiv-European Journal of Physiology] |
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| Scientists highlight the current understanding of the cellular processes that coordinate muscle regeneration, and the roles of muscle resident cells, including immune cells, fibroadipogenic progenitors, and muscle satellite cells in the pathophysiologic regulation of rotator cuff muscles following injury. [Journal of Orthopaedic Research] |
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| Sarepta Therapeutics, Inc. announced that following positive interactions with the US FDA, the Company plans to initiate Part B of the MOMENTUM study, in the fourth quarter. MOMENTUM is a global trial investigating the use of SRP-5051, the Company’s next-generation peptide-conjugated phosphorodiamidate morpholino oligomer to treat patients with Duchenne muscular dystrophy who are amenable to exon 51 skipping. [Sarepta Therapeutics, Inc.] |
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| October 4 – 6, 2021 Virtual |
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| Harvard Medical School – Boston, Massachusetts, United States |
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| Queen’s University Belfast – Belfast, Ireland |
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| Sanford Burnham Prebys Medical Discovery Institute – San Diego, California, United States |
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| European Centre Study Diabetes – Strasbourg, France |
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| Stanford University – La Jolla, California, United States |
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