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

Organotin(IV) Dithiocarbamate Compounds Targeting A549 Lung Cancer Cells via Mitochondria-Mediated Apoptosis

This study demonstrates that the newly synthesized organotin(IV) dithiocarbamate DioSn-2 exhibits potent and selective cytotoxicity against A549 lung cancer cells by inducing mitochondria-mediated apoptosis through oxidative stress and caspase-9 activation, positioning it as a promising alternative to cisplatin.

Abd Aziz, N. A., Awang, N., Kamaludin, N. F., Hamid, A., Anuar, N. N. M., Chan, K. M., Zainirizal, N. Z.2026-03-27
📄 cell biology

A general role for GGA adaptors in the modulation of AP-1-dependent trafficking

By combining CRISPR-Cas9 gene editing with live-cell imaging and proximity labeling, this study reveals that GGAs localize to distinct Golgi and peripheral compartments where they independently recruit clathrin and regulate AP-1-dependent trafficking by preventing premature AP-1 binding to its cargo, thereby modulating bi-directional transport between the Golgi and endosomes.

Stockhammer, A., Klemt, A., Daberkow, A. D., Mijatovic, J., Benz, L. S., Freund, C., Kuropka, B., Bottanelli, F.2026-03-26
📄 cell biology

Regulation of microtubule abundance and minus end dynamics by Katanin, CAMSAPs, WDR47 and kinesin-13

This study demonstrates that the interplay between the severing enzyme katanin, minus-end stabilizers CAMSAPs and WDR47, and the depolymerase kinesin-13 fine-tunes microtubule minus-end stability and abundance through a concentration-dependent balance of amplification and disassembly.

Rai, D., Radul, E., Hua, S., Spoelstra, M. F. M., Katrukha, E. A., Stecker, K. E., Jiang, K., Akhmanova, A.2026-03-26
📄 cell biology

Brieflow: An Integrated Computational Pipeline for High-Throughput Analysis of Optical Pooled Screening Data

The paper introduces Brieflow, an integrated computational pipeline for high-throughput analysis of optical pooled screening data, coupled with the MozzareLLM framework for LLM-driven biological interpretation, to overcome existing analytical challenges and uncover novel biological modules such as core mitochondrial sub-programs.

Di Bernardo, M., Kern, R., Dia, A. K. C., Mallar, A., Choi, S. J., Nutter-Upham, A., Lourido, S., Blainey, P., Cheeseman (…)2026-03-25
📄 cell biology

Comprehensive Characterization of the Human Neural Stem Cell Line HNSC.100 as a Versatile Model for Neurobiological Research

This paper provides a comprehensive characterization of the immortalized human neural stem cell line HNSC.100, validating its expression of key markers, its ability to differentiate into major neural cell types, and its genetic manipulability, while offering extensive RNA expression data and a curated list of neural disorder-related genes to establish it as a versatile and robust model for neurobiological research.

Jeruzalska, E., Ketteler, C., Stuetzenberger, E., Burczyk, S., Moeller, L., Niessing, D.2026-03-25
📄 cell biology

STING-STAT3-SOX18 Axis Drives EndMT and Epigenetic Reprogramming in SAVI Lung Fibrosis

This study reveals that gain-of-function STING1 mutations in SAVI patients drive pulmonary fibrosis by triggering a non-canonical cGAS-STING-STAT3 signaling axis that induces endothelial-to-mesenchymal transition through SLUG activation and epigenetic silencing of SOX18, independent of TGF-beta.

Yang, D., Chen, G., Gaurav, S., de Jesus, A. A., Mehta, A. K., McNinch, C., Miranda, A. X., Wei, J., Kedei, N., Hernande (…)2026-03-24