PGC-derived migrasomes couple PGC proliferation with migration
Abstract
The coordination of cell migration and proliferation is essential for embryogenesis and tissue homeostasis. However, the classical gradient signaling model is insufficient to explain how stable mitogenic signaling is maintained within migratory cells. Here, we reveal that primordial germ cells (PGCs) in zebrafish employ migrasomes—vesicular organelles formed during migration—to couple their proliferation with migration, ensuring germline expansion. Migrasomes, generated at retraction fibers via tspan7-dependent biogenesis, deliver the growth factor GDF3 specifically to neighboring PGCs through contact-dependent interactions. GDF3 activates the TGF-β receptor acvr1ba, driving proliferation in a spatiotemporally restricted manner. This homocrine signaling mechanism allows migrating PGCs to autonomously sustain proliferation, circumventing signal dilution in embryonic environments. This work uncovers migrasomes as a bridge linking migration and proliferation, with implications for understanding collective cell behaviors in development and disease. This study reveals migrating zebrafish primordial germ cells use migrasomes as mobile carriers to transport growth signals between neighbours, coupling cell migration with proliferation to ensure robust population expansion during their journey.
Fields of Study & Subjects
Developmental Biology and Gene Regulation
Neurogenesis and neuroplasticity mechanisms
Microtubule and mitosis dynamics
Publication details
- Journal / source
- Nature Communications
- Publisher
- Springer Science and Business Media LLC
- Volume
- 17
- Issue
- 1
- Publication date
- 10 April 2026
- Language
- EN