| Vol. 6.15 – 26 April, 2021 |
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| Scientists discovered a pathway connecting VPS39-deficiency in human myoblasts to impaired autophagy, abnormal epigenetic reprogramming, dysregulation of myogenic regulators, and perturbed differentiation. [Nature Communications] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Researchers investigated two possible mechanisms of arrhythmogenesis—focal vs reentrant—arising from direct remuscularization with pluripotent stem cell-derived cardiomyocyte patches in two personalized, human ventricular computer models of post-myocardial infarction. [Cardiovascular Research] |
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| circRNA regulated cardiomyocyte apoptosis and proliferation by acting as a miR-103-3p sponge and inducing increased expression of SNRK which could bind GSK3β to regulate its phosphorylated activity. [Cell Death Discovery] |
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| Researchers suggested that the increase in glucose metabolism promotes cardiac regeneration in neonatal mouse heart. [Scientific Reports] |
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| Biomaterial-based tissue engineering approaches to repair skeletal muscle are limited due to difficulties combining 3D structural alignment and electrical conductivity. Here, scientists successfully produced aligned and electrically conductive 3D collagen scaffolds using a freeze-drying approach. [Biomaterials Science] |
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| The authors assessed the impact of Staufen1 (STAU1) expression modulation in ARMS cell lines, non-transformed skeletal muscle cells and STAU1-transgenic mice using complementary techniques. [Cellular Oncology] |
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| Scientists showed that polyamine pathway enzymes were differentially regulated in models of altered mechanical and metabolic stress, and that Amd1 and SpdSyn were, in part, regulated in a mTORC1-dependent manner. [American Journal of Physiology-Cell Physiology] |
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| A model of Ang II-induced vascular smooth muscle cell (VSMC) senescence and the renal artery of hypertensive patients were used to investigate the roles and mechanisms of circACTA2 and ILF3 in VSMC senescence. Investigators showed that circACTA2 expression was elevated in Ang II-stimulated VSMCs and in the vascular walls of hypertensive patients. [Aging] |
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| Researchers show CREB phosphorylation was required for smooth muscle cell proliferation in response to platelet-derived growth factor (PDGF). This phenotypic change required CBP and was mediated by Cyclin D1 and p27kip as a result of changes in FoxO1 activity. [Experimental Cell Research] |
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| The authors review the current knowledge of fibro-adipogenic progenitor function on muscle homeostatic integrity, regeneration, repair, and aging. They also discuss how scar-forming pathologies and disorders lead to dysregulations in their behavior and plasticity and how these stromal cells can control the onset and severity of muscle loss in disease. [Frontiers in Physiology] |
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| Arrowhead Pharmaceuticals, Inc. announced ARO-human double homeobox 4 (DUX4) as Arrowhead’s first muscle targeted investigational RNAi therapeutic candidate to utilize its proprietary Targeted RNAi Molecule (TRIMTM) platform. ARO-DUX4 is designed to target the gene that encodes human DUX4 protein as a potential treatment for patients with facioscapulohumeral muscular dystrophy . [Arrowhead Pharmaceuticals] |
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| November 15 – 19, 2021 Virtual |
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| Aspect Biosystems – Vancouver, British Columbia, Canada |
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| University of Michigan – Ann Arbor, Michigan, United States |
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| Mount Sinai Health System – New York, New York, United States |
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| Stanford University – Stanford, California, United States |
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| The University of Utah School of Medicine – Salt Lake City, Utah, United States |
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