Peripheral artery disease is a common manifestation of atherosclerosis, characterized by insufficient tissue perfusion and chronic ischemia. Arteriogenesis and angiogenesis are essential endogenous mechanisms to restore blood flow and limit ischemic injury. The metalloprotease ADAMTS13, known for cleaving ultra-large von Willebrand factor, has been implicated in thrombotic and inflammatory regulation. However, its role in ischemic vascular remodeling remains unclear. Using a murine hind limb ischemia model, we investigated the effect of ADAMTS13 deficiency on arteriogenesis and angiogenesis by comparing male ADAMTS13^−/− and wild-type control mice. Perfusion recovery, vascular cell proliferation, immune cell infiltration, and thrombotic activity were evaluated using laser Doppler measurements, immunohistochemical analysis of adductor and gastrocnemius muscle tissues, and in vivo microscopy. ADAMTS13 deficiency did not impair perfusion recovery, collateral artery growth, or capillarization. While platelet adhesion was slightly increased in ADAMTS13^−/− mice, no thrombotic occlusions were observed. Inflammatory responses, including macrophage and neutrophil infiltration as well as macrophage polarization, were largely unaffected. Despite previous in vitro evidence indicating an angiogenic role for ADAMTS13, its absence did not compromise angiogenesis in vivo. Our findings suggest that ADAMTS13 does not play a critical role in ischemia-related angiogenesis and arteriogenesis under sterile conditions and may be relevant only in contexts involving acute and sufficiently strong thromboinflammatory stimuli.

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.

Arteriogenesis, the growth of pre-existing collateral arteries in response to arterial occlusion, is critically regulated by perivascular immune cells. While innate immune contributions are well-established, the role of B lymphocytes remains poorly understood. We investigated the impact of B cell deficiency on arteriogenesis using B cell-deficient J_HT mice in a murine hindlimb model of femoral artery ligation (FAL). Laser-Doppler perfusion imaging, immunofluorescence staining, Giemsa staining, flow cytometry, and differential blood counts were performed at defined time points after FAL. B cell-deficient mice exhibited significantly impaired perfusion recovery on days 3 and 7 post-FAL, accompanied by reduced collateral artery diameter growth and diminished vascular cell proliferation. Early immune analysis revealed elevated platelet–neutrophil aggregate (PNA) formation and increased perivascular mast cell degranulation in B cell-deficient mice despite unchanged circulating cell counts. On day 7, perivascular M2-like macrophage numbers were selectively reduced. Furthermore, B cell deficiency disrupted the temporal reprogramming of γδ T cell subsets, impairing the shift from pro-inflammatory IFN-γ-associated to anti-inflammatory IL-10-associated subpopulations. These findings demonstrate for the first time that B cells are essential coordinators of the sequential innate and regenerative immune response driving productive collateral artery growth, positioning them as potential targets for therapeutic arteriogenesis strategies.