Cell biology is the study of life at its most fundamental unit: the cell. This field explores how these microscopic building blocks function, communicate, and replicate to sustain living organisms, from the simplest bacteria to complex human tissues. By understanding the machinery inside a cell, scientists unlock secrets about growth, disease, and the very nature of existence itself.

At Gist.Science, we track every new preprint uploaded to bioRxiv within this dynamic category. Our team processes each submission to provide both accessible plain-language explanations and detailed technical summaries, ensuring you can grasp complex discoveries without getting lost in dense jargon. Below are the latest papers in cell biology, offering a fresh look at the inner workings of life as they are shared with the world.

📄 cell biology

Lipid transfer by ORP3 is required for the regulation of PI4P and PI(4,5)P2 at the plasma membrane in mitosis

The lipid transfer protein ORP3 regulates PI4P and PI(4,5)P2 levels at the plasma membrane during mitosis by transferring PI4P from the membrane to the ER via VAPA-mediated recruitment, a process essential for proper spindle geometry, cytokinesis, and the prevention of genetic instability.

Vertueux, A., Verraes, A., Ouaddi, C., Siegfried, H., Pellier, E., Proux-Gillardeaux, V., Walch, L., Heuze, M., Jackson (…)2026-05-12
📄 cell biology

ISWI remodeler facilitates cBAF genomic binding to drive cell fate transition

This study demonstrates that the ISWI chromatin remodeler, through its Snf2h and Snf2l subunits, is essential for cell fate transitions in muscle and adipose tissues by mediating the recruitment of the cBAF complex and CTCF to lineage-determining transcription factor binding sites, a process critical for de novo chromatin organization during differentiation.

Park, Y.-K., Lee, J.-E., Skoultchi, A. I., Picketts, D. J., Peng, W., Ge, K.2026-05-12
📄 cell biology

Quantitative analysis of fibroblast migration reveals migratory states characterized by force generation, cell shape and motion

By combining live-cell imaging, traction force microscopy, and Hidden Markov Modeling, this study reveals that fibroblast migration is organized into discrete mechanical states characterized by specific couplings of force generation, cell shape, and motion, which persist even when cytoskeletal organization is disrupted.

Davis, E. M., Hockenberry, M. A., Truscott, H. H., Shaul, N. J., Bear, J. E., Elston, T. C.2026-05-11
📄 cell biology

Liver sinusoidal endothelial cells integrate metabolic and immune signals for MAPK-dependent BMP6 regulation and hepcidin induction

This study reveals that liver sinusoidal endothelial cells integrate diverse inflammatory, metabolic, and oxidative stress signals via MAPK-dependent pathways to upregulate BMP6, which, in concert with hepatocyte secreted factors, drives hepcidin induction and subsequent hypoferremia to maintain iron homeostasis.

Qiu, R., Cucinelli, S., Mertens, C., Colucci, S., Altamura, S., Hentze, M. W., Muckenthaler, M. U.2026-05-11
📄 cell biology

Septin crosstalk with microtubules and actin is regulated by a GSK3-dependent phosphoswitch

This study reveals that glycogen synthase kinase 3 (GSK3) regulates septin 9 (SEPT9) distribution between actin and microtubule cytoskeletons through a phosphorylation-dependent switch, thereby controlling neuronal polarization and linking cytoskeletal dynamics to broader cellular signaling pathways.

Alam, M. N. A., Holt, T. C., Schaefer, A. W., Mayca-Pozo, F., Reghunathan, S., Butts, S. M., Bhakt, P., Kesisova, I. A. (…)2026-05-09
📄 cell biology

Selective Elimination of TP53 Mutant Cells by Transcript-Activated Chromatin Shredding

This study introduces a novel therapeutic strategy that utilizes RNA-guided CRISPR-Cas12a2 to selectively eliminate cancer cells harboring TP53 mutations by detecting tumor-specific transcripts to trigger trans-chromatin cleavage and cell death, thereby offering a solution for targeting previously undruggable mutations.

Zeng, J., Cheng, Z., Chen, H., Thompson, J., Crosby, K. T., Hang, H., Ngo, W., Xia, C., Rosas-Rivera, D., Kang, M. H., M (…)2026-05-09