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Liu, Y.

Publications and source records attributed to Liu, Y..

At least 667 records · Page 37Linked to original sources

scMomer: A modality-aware pretraining framework for single-cell multi-omics modeling under missing modality conditions

Foundation models offer new opportunities to capture cellular behavior from large-scale single-cell data. However, their development has been greatly constrained due to the limited availability of multi-omics profiles. Consequently, most models are designed for a single modality (e.g. scRNA-seq, or scATAC-seq, etc.), restricting their ability to capture the diversity of heterogeneous biological systems. Here, we introduce scMomer, a modality-aware pretraining framework designed for multi-modal representation learning under missing modality conditions. scMomer adopts a three-stage pretraining strategy that learns unimodal cell representations, models joint representations from multi-omics data, and distills multi-modal knowledge to enable multi-omics-like representations from unimodal input. Its modality-specific architecture and three-stage pretraining strategy enable effective learning under missing modality conditions and help capture cellular heterogeneity. Through extensive experiments, scMomer generates biologically meaningful embeddings and outperforms state-of-the-art unimodal approaches across diverse gene-level and cell-level downstream tasks, including cross-modality translation, gene function prediction, cell annotation, drug response prediction, and perturbation prediction. Overall, these results demonstrate that scMomer serves as a robust, generalizable, and scalable foundation for single-cell multi-modal analysis under missing modality conditions.

bioinformatics↗

A conserved distal element in the mouse Csf1r locus contributes to transcription in hematopoietic and trophoblast cells.

Expression of the Csf1r gene in mice is restricted to cells of the mononuclear phagocyte system and placental trophoblasts. A conserved element (Csf1r upstream regulatory element A, CUREA) in the mouse Csf1r locus contains transcription start sites utilised by trophoblasts and osteoclasts and an enhancer essential for expression of multicopy transgenic reporters in most tissue macrophages. Here we describe the impact of deletion of CUREA in the mouse genome, on the background of a knock-in Csf1r-FusionRed reporter. By contrast to the essential function in transgene expression, CUREA deletion had no effect on expression of FusionRed or differentiation of blood monocytes or tissue resident macrophages. The deletion reduced Csf1r mRNA in hematopoietic stem cells and committed myeloid progenitors (MPP3) leading to a subtle differentiation delay and also had a significant impact on microglial phenotype in the brain and the differentiation of osteoclasts. The expression of FusionRed in placenta confirmed expression of CSF1R in trophoblasts. 5RACE analysis demonstrated that the effect of CUREA deletion on Csf1r transcription in placenta was overcome by the use of cryptic upstream transcription start sites. We conclude that CUREA is a regulatory element controlling Csf1r transcription. The function overlaps with other enhancers identified in the locus and is therefore partly redundant. Key PointsO_LIA regulatory element (CUREA) in the mouse Csf1r locus has both promoter and enhancer activity. C_LIO_LIGerm-line deletion of CUREA impacts differentiation of marrow progenitors, microglia, osteoclasts and placental trophoblasts. C_LI

cell biology↗

Hedyotis Diffusae Herba Mitigates Rotenone-Induced Neurotoxicity via Akt Pathway in SH-SY5Y Cells

Hedyotis Diffusae Herba (HDH), known in traditional Chinese medicine for its heat-clearing and detoxifying properties, has been widely used to manage inflammation-related conditions. However, its neuroprotective potential and mechanism in the context of Parkinsons disease (PD) remain unclear.Network pharmacology and molecular docking were applied to predict the interactions between HDH components and PD-associated targets. Molecular dynamics simulations assessed the binding stability of major compounds to core targets. Rotenone-induced SH-SY5Y cell injury served as an in vitro PD model to evaluate HDHs biological effects. Cell viability, reactive oxygen species (ROS), IL-6 secretion, and Akt phosphorylation were assessed by CCK-8 assay, ROS detection kit, ELISA, and western blot, respectively. MK2206, an Akt inhibitor, was used to validate pathway involvement.Seven bioactive compounds were identified in HDH, among which stigmasterol and quercetin exhibited strong binding affinities with AKT1, IL-6, and JUN. Simulations confirmed stable interactions. HDH significantly increased cell viability and decreased intracellular ROS and IL-6 levels in rotenone-treated SH-SY5Y cells. Akt phosphorylation was restored by HDH, and the effect was blocked by MK2206, indicating Akt pathway participation.HDH exerts neuroprotective effects against rotenone-induced toxicity via antioxidant and anti-inflammatory activities and Akt pathway activation. These findings provide mechanistic insight and pharmacological support for HDH as a potential candidate in complementary therapy for PD.

cell biology↗

Distinguishing cortical indexes of arousal and awareness in sleeping patients with unresponsive wakefulness syndrome

Consciousness is assumed to be defined by two components: awareness and arousal. However, compared with awareness, the cortical index for arousal remains lacking in clues. Since patients with unresponsive wakefulness syndrome (UWS) are supposed to have no awareness but arousal, sleep-wake cycle in patients with UWS may reflect pure arousal fluctuations, and then could highlight the cortical indexes for arousal. This study recorded nighttime polysomnography in patients with UWS, patients with minimally conscious state and healthy controls. The EEG signal showed that spectral slope could index arousal, fluctuating among sleep stages in all three groups. Both spectral entropy and Lempel-Ziv complexity indexed awareness, showing a significant difference between conscious and unconscious states. These findings provide fundamental evidence for the two-component hypothesis of consciousness.

neuroscience↗

Iterative delivery of mRNA by MEFI

Conventional therapeutic mRNA delivery systems are inherently single-use, limiting expression potency, duration, and penetration across biological barriers. To address this, we engineered the mRNA Exporting and Ferrying Implement (MEFI), a platform that enables iterative cell-to-cell transfer of cargo mRNA, allowing a single mRNA molecule to be utilized multiple times across various cells. MEFI encodes a fusion protein that assembles virus-like particles (VLPs) and encapsulates both itself and cargo mRNA into these VLPs, orchestrating reproduction of VLPs from targeted cells and continuous intercellular spreading. MEFI significantly amplified cargo protein expression in the transfected cell populations ([~]20-fold) and in organs ([~]500-fold in lung) from mice administered systemically. Notably, through intramuscular injection of naked plasmids, MEFI promoted robust ([~]20-fold) and durable ([~]2-month) cargo expression, interorgan mRNA transfer, and successful crossing of the blood-brain barrier. Moreover, modified MEFI demonstrated cell-type-specific targeting, mediating the elimination of antigen-expressing cells. Collectively, MEFI establishes a modular platform for enhancing mRNA delivery, leveraging the concept of iterative delivery of mRNA. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=138 SRC="FIGDIR/small/667827v2_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@14522c2org.highwire.dtl.DTLVardef@1ecfa7dorg.highwire.dtl.DTLVardef@1314347org.highwire.dtl.DTLVardef@1380cc7_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗

Efficient spatial gene expression profiling using split-probe ligation and rolling circle amplification

Spatial transcriptomics has transformed our understanding of gene regulation by enabling high-resolution mapping of RNA molecules within their native cellular and tissue environments. This is typically accomplished by capturing or imaging RNA in situ, thereby preserving spatial context. Here, we introduce an in situ RNA imaging method based on split-probe ligation and rolling circle amplification (RCA) for profiling spatial gene expression. In this approach, split-probes hybridize to adjacent regions of a target RNA fragment and are then enzymatically ligated to form circular DNA templates, which are subsequently amplified via RCA to boost signal. We demonstrate that this method enables robust in situ RNA detection and genotyping in both tissue sections and whole-mount tissue samples. By coupling this technique with in situ sequencing, we mapped the spatial expression patterns of 82 genes in the kidneys of healthy and diabetic male and female mice. This analysis revealed distinct localization of Aqp4 in proximal tubules and principal cells of the collecting ducts, and uncovered sex-specific transcriptomic alterations in diabetic kidneys with spatial resolution. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=80 SRC="FIGDIR/small/668044v1_ufig1.gif" ALT="Figure 1"> View larger version (44K): org.highwire.dtl.DTLVardef@c8efaborg.highwire.dtl.DTLVardef@1eef010org.highwire.dtl.DTLVardef@1d2bbd7org.highwire.dtl.DTLVardef@2a482b_HPS_FORMAT_FIGEXP M_FIG C_FIG

biochemistry↗

Interpretable spatial multi-omics data integration and dimension reduction with SpaMV

Spatial multi-omics technologies have revolutionized our understanding of biological systems by providing spatially resolved molecular profiles from multiple perspectives. Existing spatial multi-omics integration methods often assume that data from different modalities share a common underlying distribution, aiming to project them into a single unified latent space. This assumption, however, can obscure the unique insights offered by each modality, thereby limiting the full potential of multi-omics analyses. To address this limitation, we present the Spatial Multi-View (SpaMV) representation learning algorithm, which captures both the shared information across modalities and the distinct, modality-specific information, enabling a more comprehensive and interpretable representation of spatial multi-omics data. Through extensive evaluation on both simulated and real-world datasets, SpaMV demonstrates superior spatial domain clustering performance and provides users with more interpretable dimension reduction for downstream analysis. Moreover, SpaMV effectively annotates cell types within clusters of a mouse thymus dataset, highlighting its effectiveness in interpretable dimensionality reduction.

bioinformatics↗

Discovery of chromatin-based determinants of azacytidine and decitabine anti-cancer activity

The DNA-incorporating nucleoside analogs azacytidine (AZA) and decitabine (DEC) have clinical efficacy in blood cancers, yet the precise mechanism by which these agents kill cancer cells has remained unresolved - specifically, whether their anti-tumor activity arises from conventional DNA damage or DNA hypomethylation via DNA methyltransferase 1 (DNMT1) inhibition. This incomplete mechanistic understanding has limited their broader therapeutic application, particularly in solid tumors, where early clinical trials showed limited efficacy. Here, through the assessment of drug sensitivity in over 600 human cancer models and comparison to a non-DNA-damaging DNMT1 inhibitor (GSK-3685032), we establish DNA hypomethylation, rather than DNA damage, as the primary killing mechanism of AZA and DEC across diverse cancer types. In further support of an epigenetic killing mechanism, CRISPR drug modifier screens identified a core set of chromatin regulators, most notably the histone deubiquitinase USP48, as AZA and DEC protective factors. We show that USP48 is recruited to newly hypomethylated CpG islands and deubiquitinates non-canonical histones, establishing USP48 as a key molecular link between the two components of epigenetic gene regulation: DNA methylation and chromatin modification. Furthermore, loss of USP48, which occurs naturally through biallelic deletions in human cancers, sensitized both hematologic and solid tumors to DNMT1 inhibition in vitro and in vivo. Our findings elucidate the epigenetic mechanism of action of AZA and DEC and identify a homeostatic link between DNA methylation and chromatin state, revealing new therapeutic opportunities for DNMT1 inhibitors in solid tumors.

cancer biology↗

RNA reinforces condensate nucleation on chromatin to amplify oncogenic transcription

Aberrant chromatin-associated condensates have emerged as drivers of transcriptional dysregulation in cancer. Although extensive studies have elucidated intrinsic protein sequence features governing their formation, how extrinsic factors within the chromatin environment modulate their assembly and pathogenic function remains poorly understood. Gain-of-function mutations in the histone acetylation reader ENL, found in pediatric leukemia and Wilms tumor, drive oncogenesis by inducing condensate formation at highly selective genomic loci. Here, we uncover a critical role for locally produced gene transcripts in reinforcing the nucleation, chromatin engagement, and oncogenic activity of ENL mutant condensates. Mutant ENL binds RNA in part through a conserved basic patch within its YEATS domain, and this interaction enhances condensate formation both in vitro and across diverse cellular contexts. Using a chemically inducible condensate displacement and re-nucleation system, we show that blocking ENL-RNA interactions or transcription impairs condensate reformation at endogenous targets. RNA interactions preferentially enhance mutant ENL occupancy at top-bound, condensate-permissive loci, leading to increased transcriptional bursting and robust gene activation at the single-cell and single-allele level. In mouse models, disrupting ENL-RNA interactions reduces condensate formation and oncogenic transcription in hematopoietic stem and progenitor cells, thereby suppressing ENL mutant-driven leukemogenesis. Together, these findings demonstrate that locally produced RNA transcripts can promote locus-specific nucleation of pathogenic condensates on chromatin, which in turn drive persistent and hyperactive transcription of oncogenic targets and lead to tumorigenesis.

molecular biology↗

Profiling and Functional Analysis of Urinary Exosomal MicroRNAs in Pregnant Women with Systemic Lupus Erythematosus

BackgroundPregnancy in Systemic Lupus Erythematosus (pSLE) is high-risk, necessitating non-invasive biomarkers for monitoring and predicting complications. Urinary exosomes, containing miRNAs, offer a promising source reflecting systemic and renal states, yet their profile in late gestation pSLE is less studied. ObjectiveThis study aimed to investigate the profile of urinary exosomal miRNAs in pregnant women with SLE during late gestation compared to healthy pregnant controls and to explore their potential biological roles and pathways. MethodsUrinary exosomes were isolated from 6 pSLE patients and 5 controls. Exosomes were characterized, and miRNAs were sequenced. Bioinformatics analyses, including target gene prediction and functional enrichment (GO, KEGG), were performed. ResultsExosomes were successfully isolated. Sequencing identified 29 significantly downregulated miRNAs in pSLE exosomes. Enrichment analysis of these miRNAs and their target genes indicated involvement in metabolic and immune pathways, virus infection, and cellular senescence. Target genes also enriched in protein stability and transport, and high-level analysis showed broader roles in metabolic, immune, and cellular maintenance/stress processes. Targets of top differentially expressed miRNAs linked to mRNA regulation, AMPK, and senescence pathways. ConclusionOur findings demonstrate that urinary exosomal miRNAs are significantly altered in pregnant women with SLE during late gestation. The functional enrichment analysis suggests their target genes are involved in critical biological processes relevant to pSLE pathophysiology and pregnancy complications, including metabolism, immunity, viral response, senescence, and cellular maintenance. This highlights the potential of urinary exosomal miRNAs as non-invasive biomarkers for monitoring and predicting risks in this high-risk population.

immunology↗

Histone Acetylation Differentially Modulates CTCF-CTCF Loops and Intra-TAD Interactions

The cohesin complex structures the interphase genome by extruding loops and organizing topologically associating domains (TADs). While cohesin engages chromatin in context- dependent modes, the regulatory influence of chromatin state on these interactions remains unclear. Here, we show that histone hyperacetylation, induced by the histone deacetylase inhibitor trichostatin A (TSA), preferentially disrupts short-range interactions within TADs but spares CTCF-anchored loops, despite reduced cohesin occupancy at these sites. These findings point to two functionally distinct cohesin populations: a TSA- sensitive pool within TADs, likely representing extruding, non-topologically bound cohesin, and a TSA-resistant population at CTCF-CTCF anchors that maintains loops through topological entrapment. Using a semi-in vitro system with TEV-cleavable RAD21, we show that TSA-resistant cohesin at CTCF sites becomes TSA-sensitive after proteolytic cleavage that opens the cohesin ring, showing that it is the topological engagement with DNA that makes cohesin, and CTCF-CTCF loops, TSA-resistant. Notably, we also detect TSA-sensitive cohesin at CTCF sites, suggesting the presence of transient, non-encircling cohesin that either precedes conversion to the stable form or is halted by pre-existing encircling cohesin. Together, our results suggest that cohesin exists in distinct biochemical states: an extruding form found within TADs and at CTCF sites, that is sensitive to hyperacetylation, and a topologically bound form specifically at CTCF-CTCF loops that is insensitive. The former may allow dynamic changes in chromatin loops, while latter ensures robustness of CTCF-anchored loops in response to chromatin state changes.

genomics↗

Determine Protein Interaction Affinity without Purification Reveals a Two-enzyme Co-recognition of SUMOylation Substrate using Quantitative FRET (qFRET) Technology

Protein-protein interaction is the most fundamental process in life, and the quantification and manipulation of protein interaction activation or inhibition are critical for a comprehensive understanding of physiological processes and the development of new medicines that modulate protein-protein interactions. Due to its essential roles in physiology and pathology, many methodologies and technologies have been developed to determine the interaction events and parameters of interaction affinity. However, due to the nature of these methodologies, interactive partner needs to be purified, and large quantities of proteins are needed. This significantly limits quantitatively understanding of protein interaction and its application in therapeutics development. Recently, a quantitative FRET(qFRET) method was developed to determine purified protein-protein interaction affinity for purified proteins in vitro. Here, for the first time, we report the development of a high-throughput approach to determining the protein interaction affinity between two un-purified proteins using a quantitative FRET assay(qFRET). Two proteins, SUMO E2 conjugating enzyme, Ubc9, and RanGap1c, were first employed for the methodology development. We then determined the interaction affinities of Ubc9 and PIAS1 with influenza A virus NS1 protein without purifying two interactive partners. We found that both enzymes have high affinities to interaction affinity to the NS1, and this provides a kinetics explanation for the SUMOylation two-enzyme co-recognition mechanism to achieve high substrate specificity in vivo. The protein interaction affinity determination without purification provides several advantages over the current methods, including high accuracy, no tedious protein purification process, and high-throughput assay. The novel approach, so-called High-throughput determination of protein interaction affinity, KD, without purification using quantitative FRET assay, and scientific discoveries, representing a significant advancement in technology and scientific discovery, holds great potential for large-scale protein-protein interaction affinity determinations in vitro and in vivo. TeaserA novel qFRET technology for protein interaction affinity determination without protein purification for two-enzyme recognition.

bioengineering↗

Human hippocampal ripples prioritise model-based learning

Humans often learn optimally, inferring the value of options they have never directly experienced by leveraging internal models of the world, a process known as model-based learning. Yet how the brain decides which unexperienced options to update first remains unclear. Here we recorded intracranial EEG from 34 epilepsy patients performing a reinforcement-learning task that required using task structure to infer the value of unvisited (non-local) paths. After each reward, brief hippocampal "ripple" events signalled which indirect experience was most valuable, thereby encoding that paths priority. Longer ripples carried the strongest priority signals, allowing the brain to update high-value, unvisited options first and thereby optimise learning. Ripple events also coincided with selective cortical reactivation of these high-priority paths, consistent with prioritised replay. Crucially, when hippocampal ripples were precisely synchronised with activity in the lateral frontopolar cortex (LFPC), individuals showed greater model-based learning: stronger ripple-LFPC coupling predicted more effective use of task structure and more accurate learning of non-local values. Our findings establish hippocampal ripple-centred prefrontal coordination as a fundamental mechanism that prioritises valuable experiences for model-based learning, explaining how the human brain learns so efficiently.

neuroscience↗

Molecular noise modulates transitions in the cell-fate differentiation landscape

Waddingtons epigenetic landscape has become one of biologys cornerstone metaphors, widely used both conceptually and computationally. Cell types are often associated with the stable stationary points or valleys of this landscape. In previous work, we showed that the molecular noise dominating sub-cellular dynamics can distort and profoundly reshape this landscape. In non-equilibrium systems, an equally profound question arises: to what extent does noise alter the transition paths between valleys in such dynamic landscapes. We tackle this question using a set of illustrative exemplars, and show that noise gives rise to paths that differ substantially from the canonical least-action paths calculated under deterministic dynamics. We dissect the dynamics of these exemplars and determine the reactive density and transition currents, which show us, respectively, where and how transitions occur for different realisations of stochastic dynamics. Our analysis unambiguously demonstrates that reaction paths for stochastic dynamics diverge non-trivially from their deterministic least-action paths or simple barrier crossing models.

developmental biology↗

Intracellular auto-circularizing RNA using human tRNA splicing elements

Circular RNAs (circRNAs), a type of covalently closed RNA, have emerged as crucial regulatory factors in gene expression and development across various organisms. Understanding their formation and functional mechanisms holds potential for therapeutic applications, including novel RNA vaccines against diseases such as COVID-19. However, practical challenges still exist in the preparation of circRNAs. In this study, we explored the influence of human tRNA splicing elements on circRNAs formation and identified effective sequences for intracellular auto-circularization. We developed a generic auto-circularizing RNA (acRNA) framework template, optimized various key components of circRNAs formation, and proposed a more efficient and precise intracellular auto-circularization method. This study provides novel insights into the production mechanism of circRNA and establishes a simple and effective method for intracellular auto-circularization.

cell biology↗

MSF-CPMP: A Novel Multi-Source Feature Fusion Model for Prediction of Cyclic Peptide Membrane Permeability

Cyclic peptides are becoming attractive molecules for drug discovery because of their properties with inherent stability and structural diversity. However, the high potential of cyclic peptide drugs is challenged by the limited membrane permeability cross cell membrane. To predict cyclic peptide membrane permeability (CPMP), an increased number of computational models or tools are designed and used. But these existing algorithms or models do not appropriately capture feature diversity of cyclic peptides. In this study, we introduce a novel multi-source feature fusion model called MSF-CPMP, which aims to increase the accuracy of predicted CPMP. The MSF-CPMP model incorporates three features extracted from SMILES sequences, graph-based molecular structures, and physicochemical properties of cyclic peptides. By benchmarking with other machine learning and deep learning-based methods, MSF-CPMP achieved the highest levels of the evaluation metrics such as accuracy of 0.9062 and AUROC of 0.9546, and further validated MSF-CPMP robustness in learning capabilities and efficacy of its multi-source fusion. Our result demonstrates that MSF-CPMP outperforms other methods in predicting CPMP, that provides also exemplifies the power of advanced deep learning methods in tackling complex biological challenges, offering contributions to computational biology and clinical treatment. Code is available at https://github.com/wanglabhku/MSF-CPMP Author summaryWe have recognized that cyclic peptides are one type of main macro-molecular drugs useful for treatment of human diseases. However, the structural diversity of cyclic peptides results in limited permeability across cell membranes which is challenging drug research or industrial development. Previously some computational models or tools including machine learning or deep learning ones tried to solve this problem, but they still are not efficient. There are urgent requirement for more effective methodologies. Thus, we introduce a novel multi-source feature fusion model called MSF-CPMP. Our aim is to enhance accuracy and efficiency of predicted CPMP. We carried out evaluation of performance metrics by comparative analysis between MSF-CPMP and other machine learning or deep learning methods. Our result demonstrates that MSF-CPMP outperforms other models in predicting CPMP. We further validated MSF-CPMP robustness in learning capabilities and efficacy of its multi-source feature fusion. In the future we would further improve our methods that can integrate broader biomedicine and biomedical information and provide guide for drug diversity in clinically treating complex human diseases.

bioinformatics↗

DNAH14 deficiency impairs sperm motility by reducing flagellar beat amplitude

Male infertility affects approximately 15-20% of couples worldwide, with asthenozoospermia accounting for 19% of cases. Nevertheless, the genetic basis of many asthenozoospermia cases remains poorly understood. In this study, we generated Dnah14 knockout mice, which displayed subfertility due to impaired sperm motility despite normal sperm morphology. Comprehensive kinematic analysis revealed that Dnah14-deficient spermatozoa exhibited reduced flagellar beat amplitude but increased beat frequency, while other dynein components remained unaffected. Notably, increasing sperm concentration during in vitro fertilization (IVF) experiments partially rescued the fertilization defects caused by Dnah14 deletion, suggesting a compensatory mechanism for this specific form of asthenozoospermia. Our results establish DNAH14 as a critical regulator of sperm motility and propose a potential therapeutic strategy for affected individuals.

developmental biology↗

A critical contribution of cardiac myofibroblasts in right ventricular failure and the role of UCP2 SNPs in the predisposition to RV decompensation in pulmonary arterial hypertension

The mechanism of transition from compensated (cRV) to decompensated right ventricle (dRV) in pulmonary arterial hypertension (PAH) is unknown. We explored the role of RV cardiac myofibroblasts (cMFB) on this transition utilizing a rat model and 3 cohorts of 81 patients which included clinical data, RV tissues and blood. We hypothesized that the loss of UCP2, critical for mitochondrial calcium (mCa++) regulation and cardiac fibroblasts (cFB) differentiation, is associated with dRV in rats and humans; and that a loss-of-function UCP2 SNP (rs659366) may predict dRV in human PAH. We separated rat cRV from dRV based on catheterization and echocardiographic criteria and found a significant increase in cMFB in dRV. In isolated hearts, RV contractility was lower in dRV but not in isolated cardiomyocyte (CM), pointing to a non-CM cause. Mitochondrial respiration was lower in dRV cMFB than in control and cRV cFB. mCa++ was progressively decreased from normal to cRV to dRV c(M)FB, and the same was true for c(M)FB (but not CM) UCP2 levels. Human PAH, but not secondary pulmonary hypertension, dRVs had more cMFB and less UCP2 than control and cRVs. Decreased UCP2 (protein and mRNA) levels and the presence of heterozygous/homozygous UCP2 SNP were associated with worse RV performance (TAPSE, cardiac index), even among patients with similar mean pulmonary arterial pressure. Our data point to a change of cell identity (cFB to cMFB) in the RV as a driver of RV decompensation. UCP2 SNPs are promising biomarkers for early cRV transition to dRV in PAH.

molecular biology↗