Search bioRxiv⌕ Search

Biology subjects

Yu, F.-L.

Publications and source records attributed to Yu, F.-L..

2 recordsLinked to original sources

CAPTAIN: A multimodal foundation model pretrained on co-assayed single-cell RNA and protein

Proteins act as the terminal effectors of cellular function, encoding the phenotypic consequences of genomic and transcriptomic programs. Although transcriptomic profiles serve as accessible proxies, they remain incomplete surrogates for the proteomic landscape that ultimately defines cellular phenotypes. Current single-cell foundation models, however, are trained exclusively on transcriptomes, resulting in biased and partial characterizations of cellular states. To address this limitation, we introduce CAPTAIN, a multimodal foundational model pretrained on over four million single cells with concurrently measured transcriptomes and a curated repertoire of 382 surface proteins across diverse human and mouse tissues. Our results show that CAPTAIN learns unified multimodal representations by modeling cross-modality dependencies and capturing the diversity of cellular states across complex biological contexts. CAPTAIN generalizes robustly across both fine-tuning and zero-shot settings, excelling in core downstream tasks such as protein imputation and expansion, cell type annotation, and batch harmonization. Beyond improved accuracy in multi-omics integration, CAPTAIN uncovers previously inaccessible mechanisms of protein-driven intercellular dynamics, including immune interaction patterns linked to COVID-19 severity. CAPTAIN establishes a new paradigm for multimodal single-cell modeling, laying the foundation for comprehensive cellular understanding and virtual cell construction.

bioinformatics↗

The Effect of Arsenic on Mitochondrial Fatty Acid Metabolism via Inhibition of Carnitine Palmitoyltransferase 1B and Choline Kinase Beta in C2C12 Cells

Arsenic can enter the human body through environmental exposure via food, drinking water, and chemotherapy for cancer. Prolonged and excessive exposure to arsenic causes various toxic reactions, leading to diseases that significantly impact health and lifespan. Increasing evidence suggests that arsenic damages skeletal muscle tissue by reducing muscle mass and causing atrophy, thereby contributing to conditions such as respiratory and cardiovascular diseases, as well as diabetes. Fatty acid {beta}-oxidation is the most efficient mechanism for ATP production and serves as a primary energy source for tissues, including the heart and skeletal muscles. However, the metabolic mechanisms underlying arsenics effects on muscle function and pathogenesis remain incompletely understood. In this study, we investigated the role of mitochondrial fatty acid oxidation in arsenic-induced muscular damage using mouse skeletal muscle C2C12 cells. Our results demonstrated a dose-dependent inhibitory effect of sodium arsenite (0-2 {micro}M, 72 hours) on C2C12 cells proliferation, viability, and differentiation (indicated by reduction of myogenic differentiation 1 mRNA expression). Arsenic exposure disrupted mitochondria through increasing reactive oxygen species production, reducing mitochondrial membrane potential, downregulating mitochondrial fatty acid metabolism-related enzymes (carnitine palmitoyltransferase 1B and choline kinase beta mRNA), and decreasing mitochondrial DNA copy number. These findings suggest that arsenic-induced pathological changes in skeletal muscle are associated with impaired mitochondrial membrane function, disrupted fatty acid metabolism, and reduced mitochondrial DNA content in muscle cells.

cell biology↗