In vivo study reveals enhanced wound repair in zebrafish lacking Rhbdl2 via Rac2-driven macrophage migration, suggesting a target for controlling tissue regeneration.
Wound repair requires tight control of immune cell behavior, yet the mechanisms that restrain immune-driven wound repair responses remain poorly defined. Here, we demonstrate that rhomboid intramembrane serine protease Rhbdl2 influences wound repair in zebrafish. We generated rhbdl2 mutants using CRISPR-Cas9 and found that, although Rhbdl2 is dispensable for normal development, its loss triggers enhanced wound repair following injury. This regenerative phenotype is accompanied by increased macrophage migration speed and accumulation at the wound site, as well as elevated early apoptosis and cell proliferation. Proteomic analyses reveal increased Rac2 protein levels in rhbdl2 mutants, which was previously identified as a regulator of leukocyte motility. Functionally, Rac2 morpholino-mediated knockdown in rhbdl2 mutant larvae suppresses the elevated macrophage recruitment and enhanced tissue repair phenotype. Together, these findings identify Rhbdl2 as a modulator of macrophage recruitment to the wound site during tissue repair, with implications for inflammatory disease, fibrosis, and tumor-immune interactions.
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Gourkanti et al. (2026) studied this question.
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