Monolayers of confluent elongated cells are frequently considered active nematics, featuring \(\pm \frac{1}{2}\) topological defects. In extensile systems, where cells extend further along their long axis, they can accumulate at \(+\frac{1}{2}\) defects and escape from \(-\frac{1}{2}\) defects. Nevertheless, collective dynamics surrounding integer defects remain insufficiently understood. We induce diverse + 1 topological defects (asters, spirals, and targets) within neural progenitor cell monolayers using microfabricated patterns. Remarkably, cells migrate toward the cores of all + 1 defects, challenging existing theories and conventional extensile/contractile dichotomy, which predicts escape from highly bent spirals and targets. By combining experiments and a continuum theory derived from a cell-level model, we identify previously overlooked nonlinear active forces driving this unexpected accumulation toward defect cores, providing a unified framework to explain cell behavior across defect types. Our findings establish + 1 defects as probes to uncover key nonlinear features of active nematics, offering a methodology to characterize and classify cell monolayers.
