PGC-derived migrasomes couple PGC proliferation with migration

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Authors: Boqi Liu, Zheng Jiang, Wenhao Song, Zhaocheng Zhai, Yaqi Li, Weiying Zhang, Anming Meng, Li Yu
Cited by: 2
References: 57

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