Yibin Wang's research while affiliated with Duke-NUS Medical School and other places

Publications (9)

Article
Full-text available
BACKGROUND Cardiac fibrosis is a common pathological feature associated with adverse clinical outcome in postinjury remodeling and has no effective therapy. Using an unbiased transcriptome analysis, we identified FMO2 (flavin-containing monooxygenase 2) as a top-ranked gene dynamically expressed following myocardial infarction (MI) in hearts across...
Article
Background: Heart failure (HF) is a highly heterogeneous disorder characterized by the interactions of multiple genetic and environmental factors as well as the interaction of different cell types in the heart. Although reductionistic approaches have successfully identified many genes involved in HF, heritability studies suggest that many genes hav...
Article
Post-transcriptional regulation plays a key role in transcriptome reprogramming during cardiac pathogenesis. In previous studies, we have identified that cardiac enriched RNA-binding protein, RBFox1 plays key role in cardiac hypertrophy through mRNA alternative splicing regulation in nuclei. However, RBFox1 gene also generates a cytosolic isoform (...
Article
Heart failure with preserved ejection fraction (HFpEF) is an emerging form of heart failure worldwide with no effective therapies in contrast with heart failure with reserved ejection fraction (HFrEF). To simulate multiple risk-factors associated with HFpEF in clinic, we developed a HFpEF mouse model by introducing cardiac hypertrophy with transver...
Article
Background Human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have emerged as a promising tool for disease modeling and drug development. However, hiPSC-CMs remain functionally immature, which hinders their utility as a model of human cardiomyocytes. Objective To improve the electrophysiological maturation of hiPSC-CMs. Method...
Article
The central dogma of molecular biology illustrates the importance of messenger RNAs as critical mediators between genetic information encoded at the DNA level and proteomes/metabolomes at the cellular and organ levels. Although the total number of protein-producing (coding) genes in the mammalian genome is approximately 20,000, it is evident that t...
Article
The maturation of stem cell derived cardiomyocytes (iCMs) is incomplete relative to the fully matured adult myocytes. Lack of maturation represents a major limitation to the applications of iCMs as heart disease models or heart failure therapies. Current attempts to promote iCMs maturation, such as prolonged culture, mechanical stretching and elect...
Article
Background: Cardiovascular disease is the leading cause of death in the world with a dearth of effective therapies. Heart undergoes a complex differentiation and maturation process throughout embryonic and post-natal stages. Intense efforts have been made in the study of cardiomyocyte differentiation, maturation and pathological remodeling. With th...

Citations

... Figure 4B further support that under the background of normal mice, the process of Pg-induced elevated plasma TMAO levels depends more on the oxidation of TMA in the liver rather than the generation of TMA in the intestine. Pg, Fn, and Sm groups exhibited a downregulation in FMO2 gene expression compared to the control group, which potentially indicates a general stress response of the liver to oral pathogenic bacterial infection (Ni et al., 2022). In vitro TMAO exacerbates lipid accumulation, inflammation, and fibrosis in the liver (Vallianou et al., 2019;Carpino et al., 2020). ...
... In such preparations, the preservation of electrical coupling between cells means that electrophysiological recordings reflect the summation of a wider pool of currents which influence the measured membrane potential 26,27 . Additionally, experiments on isolated iPSC-CMs typically involve prolonged periods of culture as single cells 10,22,27 . This is known to promote electrophysiological remodelling in isolated adult CMs and may therefore contribute to the heterogeneity exhibited by isolated iPSC-CMs 28-30 . ...
... Dysregulated mechanistic target of rapamycin (mTOR) and insulin-like growth factor 1 (IGF1) signaling, impaired nutrient sensing, and autophagy are implicated in the pathogenesis of progeroid syndromes, laminopathies, as well as aging in the general population. Genetic and pharmacological inhibition of the mTOR signaling pathways, as well as intermittent fasting and restriction of branched-chain amino acids, are shown to increase life span, including in a mouse model of progeria, and reduce age-related diseases [39][40][41][42][43] . The genome is not only affected by the mutations but also by various endogenous, such as reactive oxygen species, and exogenous, such as ultraviolet light, resulting in various forms of DNA damage, most notably doublestranded DNA breaks (DSBs). ...
... Numerous prior studies have investigated the mRNA and miRNA as integral players in the cardiovascular system's physiological and pathophysiological processes (84,85). It is necessary to investigate further the relationship between SFⅡ helicases (such as Dicer and RHAU) and miRNA and mRNA in mixed primary cardiomyopathies, including DCM. ...
... 185 The RNA splicing regulator RBFOX1 (RNA-binding Fox-1 homolog 1) markedly increases in expression during cardiomyocyte maturation 180,186 and is another potential activator of cardiomyocyte maturation. 187 MicroRNA (miRNA)-based mRNA silencing is another mechanism that modulates gene expression in cardiomyocyte maturation. For example, miR-1, a miRNA enriched in mature cardiomyocytes, facilitated electrophysiological maturation in stem cell-derived cardiomyocytes in vitro. ...