bims-evecad Biomed News
on Extracellular vesicles and cardiovascular disease
Issue of 2026–08–23
three papers selected by
Cliff Dominy



  1. J Extracell Biol. 2026 Aug;5(8): e70179
      Takayasu arteritis (TAK) is a large-vessel vasculitis that can lead to aneurysmal dilation, yet reliable circulating biomarkers for vascular remodelling remain lacking. Extracellular vesicles (EVs) carry miRNAs implicated in vascular biology, but their relevance to TAK has not been fully explored. Circulating EVs were isolated from serum of 54 patients with TAK and healthy controls (HC), characterized, and profiled for miRNA content. Effects on endothelial cells (ECs) and monocytes were examined in vitro, and the diagnostic performance of EV-associated miR-223-3p for aortic dilation was assessed by ROC analysis. Circulating EVs from patients with TAK exhibited a distinct miRNA profile compared with HC. HC-EVs reduced the transcript abundance of ICAM-1 and VCAM-1 in ECs, an effect attenuated in TAK-EVs and accompanied by enhanced monocyte adhesion. EV-derived miR-223-3p was upregulated in TAK but selectively downregulated in patients with aortic dilation. EV-associated miR-223-3p discriminated aortic dilation with an AUC of 0.748, exceeding that of CRP and ESR. Flow cytometric profiling revealed a reduction in platelet-derived EVs in patients with aortic dilation. Reduced EV-associated miR-223-3p is associated with aortic dilation in TAK and may serve as a candidate biomarker as an adjunct to imaging-based assessment, warranting prospective validation in larger cohorts.
    Keywords:  MicroRNA‐223‐3p; Takayasu arteritis; extracellular vesicles; platelet‐derived EVs; vascular remodelling
    DOI:  https://doi.org/10.1002/jex2.70179
  2. Front Cell Dev Biol. 2026 ;14 1844243
      Atherosclerosis is a progressive inflammatory vascular disease, and its acute clinical consequences-myocardial infarction and ischemic stroke-are the principal cause of cardiovascular mortality globally. Plaque rupture, driven by dysregulated immune activity within the plaque microenvironment, is the immediate precipitant of acute cardiovascular events. Single-cell RNA sequencing, spatial transcriptomics, and high-resolution mechanobiology have shown that atherosclerotic plaques are spatially organised structures in which functionally divergent cell populations occupy the fibrous cap, necrotic core, shoulder region, and neovascularisation zone-a heterogeneity organised by two regulatory axes: mechanotransduction and vesicular trafficking. This review elucidates how the mechano-vesicular dual-axis shapes the plaque immune microenvironment and drives the transition from stable to vulnerable plaque phenotype, and assesses the translational potential of the framework for precision diagnostics and therapeutics. We here formally propose the Mechano-Vesicular Dual-Axis (MVDA) model as a unifying conceptual framework for plaque immune microenvironment organisation, defined by three constitutive elements: (i) a mechanotransduction axis converting hemodynamic and matrix-stiffness cues into intracellular signaling; (ii) a vesicular trafficking axis propagating mechanically-encoded information across cells; and (iii) bidirectional coupling through shared signaling nodes (KLF2/4, YAP/TAZ, NF-κB, PI3K/Akt/mTOR). To our knowledge, this is the first explicit integration of these two regulatory axes into a single testable framework for plaque spatial biology. Oscillatory shear stress and progressive matrix stiffening reprogramme endothelial cells, macrophages, and vascular smooth muscle cells through mechanosensors including Piezo1, integrins, and YAP/TAZ, driving pro-inflammatory gene programmes and spatially directed immune cell migration. Extracellular vesicles (EVs) generated under distinct mechanical stimuli carry bioactive cargo-including miR-155, miR-146a, oxidised phospholipids, and damage-associated molecular patterns-that establishes paracrine and long-range intercellular communication networks propagating mechanical activation signals. The two axes are connected through shared signaling nodes (KLF2/4 as an upstream flow-sensitive gate; YAP/TAZ and NF-κB as parallel effectors; PI3K/Akt/mTOR as vesicular output controllers). Dysregulation manifests as elevated pro-inflammatory EV output, macrophage and T cell accumulation at the shoulder region, impaired efferocytosis, and progressive fibrous cap thinning, marking the mechanistic transition toward the vulnerable plaque phenotype. The MVDA model suggests a move from systemic pharmacological intervention toward spatially precise targeting of mechanically high-risk microregions. Translational candidates include Piezo1 antagonists, YAP/TAZ inhibitors delivered via biomimetic nanoparticles, engineered M2 macrophage-derived EVs, and circulating EV-encapsulated miRNA panels as non-invasive biomarkers of plaque vulnerability. The MVDA model's mechano-immune scaffold is substantially supported by human data; its vesicular reverse-coupling claims remain forward-looking and await in vivo genetic validation. Addressing methodological challenges-real-time mechanical signal quantification, standardised EV tracking, and the murine-to-human translational gap-will be central to the next phase of work.
    Keywords:  Piezo1; YAP/TAZ; atherosclerosis; efferocytosis; extracellular vesicles; immune microenvironment; mechanotransduction; plaque spatial architecture
    DOI:  https://doi.org/10.3389/fcell.2026.1844243
  3. Transl Stroke Res. 2026 Aug 21. pii: 98. [Epub ahead of print]17(5):
      Sphingolipids critically regulate microvascular integrity and function, but the role of glycosphingolipids in endothelial survival and angiogenesis remains poorly defined. Herein, we experimentally deactivated or activated UDP-glucose ceramide glucosyltransferase (UGCG), which converts ceramide to glucosylceramide, by the pharmacological inhibitor D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP), siRNA-mediated knockdown or the pharmacological activator L-PDMP. Sphingolipid and glycosphingolipid profiles were examined by liquid chromatography-tandem-mass spectrometry. Effects on endothelial survival, proliferation, transwell migration, extracellular vesicle (EV) release and tube formation were assessed in human cerebral microvascular endothelial cells (hCMEC/D3). In vitro, pharmacological UGCG deactivation near-completely suppressed hexosylceramide levels and at high dose increased ceramide and sphingosine-1-phosphate (S1P), a known pro-angiogenic sphingolipid, while UGCG knockdown moderately decreased mostly short (C16, C18) hexosylceramides. UGCG activation increased hexosylceramide without significantly altering ceramide and S1P. Pharmacological UGCG deactivation increased endothelial tube formation, a marker of angiogenesis, but at high dose decreased endothelial survival, whereas UGCG knockdown and UGCG activation reduced endothelial tube formation and migration or proliferation, respectively. Pharmacological UGCG deactivation and activation, but not UGCG knockdown increased endothelial release of EVs with anti-angiogenic activity. In mice exposed to transient middle cerebral artery occlusion, pharmacological UGCG deactivation and activation reduced the length and branch density of small-sized (< 4 µm) and intermediate (4-5.4 µm) cerebral microvessels in the reperfused striatum as revealed by 3D light-sheet microscopy, indicative of microvascular endothelial degeneration. Our results suggest that pharmacological UGCG deactivation promotes angiogenesis in vitro probably via S1P elevation. In vivo, UGCG deactivation failed to stabilize microvascular network integrity post-ischemia/reperfusion, presumably due to ceramide-associated cell stress.
    Keywords:  Exosomes; Glycosphingolipids; Ischemic stroke; Light-sheet microscopy; Microvascular remodeling; Middle cerebral artery occlusion
    DOI:  https://doi.org/10.1007/s12975-026-01488-9