Research (Wash D C). 2025 Dec 22;8:1050. doi: 10.34133/research.1050. eCollection 2025.
ABSTRACT
Early mammalian embryos undergo crucial cell divisions despite lacking fully functional centrosomes, presenting a paradox of how mitotic fidelity is maintained. This commentary discusses a seminal study by Hernandez et al. that overturns the microtubule-centric model of early embryonic mitosis by revealing 2 essential, complementary F-actin networks. First, a formin-dependent nuclear F-actin network, cross-linked by anillin, positions prophase chromosomes and then drives their centripetal congregation upon nuclear envelope breakdown via a novel depolymerization-based contraction mechanism. Second, a branched, Arp2/3-dependent peri-spindle actin shell acts as a physical brake to restrain spindle elongation. Using advanced live imaging and targeted perturbations in mouse and human embryos, the study demonstrates that these actin assemblies collectively ensure accurate chromosome segregation by compensating for weak centrosomal activity. These findings redefine the mechanical landscape of early embryonic cell division, with profound implications for understanding the origins of aneuploidy and advancing reproductive medicine.
PMID:41438950 | PMC:PMC12719554 | DOI:10.34133/research.1050