Wimmer KS, Baur C, Kübler M, Arnholdt C, Kumaraswami K, Heim F, Elbs K, Rohrmoser MR, Merkus D, Deindl E (2026)
Publication Type: Journal article
Publication year: 2026
Book Volume: 15
Journal Issue: 8
Despite the identification of several mediators of arteriogenesis, the growth of natural bypass, the role of lymphocytes, particularly T cells, in this process remains poorly defined. Among these, γδ T cells, which express alternative T cell receptors, have emerged as a key immune component. This study examined the roles of αβ and γδ T cells in arteriogenesis using a murine hindlimb model. While the absence of αβ T cells did not affect arteriogenesis, γδ T cell depletion markedly reduced vascular cell proliferation and perfusion recovery. Early phase analyses revealed impaired mast cell activation, whereas platelet-neutrophil aggregates and neutrophil extravasation were unaffected. In the later proliferative phase, γδ T cell depletion hindered perivascular M2-like (MRC1+) macrophage accumulation. Flow cytometric analysis of whole blood in wildtype mice revealed a temporal shift in γδ T cell populations from a CD27+/CD39- phenotype, commonly associated with pro-inflammatory functions and IFNγ production, to CD39+ phenotypes, which have been linked to anti-inflammatory properties and IL-10 production. In rescue experiments, administration of IFNγ to γδ T cell-depleted mice restored mast cell activation, whereas IL-10 treatment reestablished M2-like (MRC1+) macrophage accumulation. These findings collectively identify γδ T cells as critical regulators of both early and late phases of arteriogenesis through coordinated inflammatory and regenerative mechanisms.
APA:
Wimmer, K.S., Baur, C., Kübler, M., Arnholdt, C., Kumaraswami, K., Heim, F.,... Deindl, E. (2026). Small Subset, Big Impact: Regulatory Function of γδ T Cells in Arteriogenesis. Cells, 15(8). https://doi.org/10.3390/cells15080709
MLA:
Wimmer, Kira Sofie, et al. "Small Subset, Big Impact: Regulatory Function of γδ T Cells in Arteriogenesis." Cells 15.8 (2026).
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