10,522 results match your criteria: "Arteriosclerosis Thrombosis and Vascular Biology[Journal]"

Background: Evidence suggests that the intrauterine environment shapes offspring cardiovascular disease risk. Although placental dysfunction may be an important pathophysiologic pathway, numerous parental and pregnancy characteristics that influence offspring blood pressure are strong confounders of the mechanistic role of the placenta in observational analyses of singletons. Therefore, we leverage twin- and sibling-based comparison designs to determine whether placental pathology is associated with offspring blood pressure at age 7 while mitigating major sources of confounding.

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Background: Smooth muscle cells (SMCs) of cardiac and neural crest origin contribute to the developing proximal aorta and are linked to disease propensity in adults.

Methods: We analyzed single-cell transcriptomes of aortic SMCs from adult mice to determine basal states and changes after disrupting TGFβ (transforming growth factor-β) signaling necessary for aortic homeostasis.

Results: A minority of Myh11 lineage-marked SMCs differentially expressed genes suggestive of embryological origin.

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Background: Coronary artery disease is the leading cause of death worldwide. It imposes an enormous symptomatic burden on patients, leaving many with residual disease despite optimal procedural therapy and up to one-thirds with debilitating angina amenable neither to procedures, nor to current pharmacological options. Semaglutide (SEM), a GLP-1 (glucagon-like peptide 1) agonist originally approved for management of diabetes, has garnered substantial attention for its capacity to attenuate cardiovascular risk.

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Decreased Adipose Lipid Turnover Associates With Cardiometabolic Risk and the Metabolic Syndrome.

Arterioscler Thromb Vasc Biol

December 2024

Department of Medicine H7, C2:94 Karolinska Institutet, Stockholm, Sweden. Department of Endocrinology, C2:94 Karolinska University Hospital, Stockholm, Sweden.

Background: Disturbed white adipose tissue function is important for cardiometabolic risk and metabolic syndrome (MetS). Whether this involves adipose lipid turnover (lipolysis and synthesis of triglycerides) is unknown and was presently investigated in subcutaneous adipose tissue, the body's largest fat depot.

Methods: In cross-sectional studies in 78 subjects, adipose lipid age, representing overall lipid turnover (mobilization and storage), and lipid storage capacity were assessed by the incorporation of atmospheric C into adipose lipids.

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Extracellular Vesicles From Preeclampsia Disrupt the Blood-Brain Barrier by Reducing CLDN5.

Arterioscler Thromb Vasc Biol

December 2024

Vascular Physiology Laboratory, Department of Basic Sciences, Universidad del Bío-Bío, Chillán, Chile (H.S., B.I., M.C., F.T., E.E.-G., J.A., C.E.).

Background: The physiopathology of life-threatening cerebrovascular complications in preeclampsia is unknown. We investigated whether disruption of the blood-brain barrier, generated using circulating small extracellular vesicles (sEVs) from women with preeclampsia or placentae cultured under hypoxic conditions, impairs the expression of tight junction proteins, such as CLDN5 (claudin-5), mediated by VEGF (vascular endothelial growth factor), and activation of KDR (VEGFR2 [VEGF receptor 2]).

Methods: We perform a preclinical mechanistic study using sEVs isolated from plasma of pregnant women with normal pregnancy (sEVs-NP; n=9), sEVs isolated from plasma of women with preeclampsia (sEVs-PE; n=9), or sEVs isolated from placentas cultured in normoxia (sEVs-Nor; n=10) or sEVs isolated from placentas cultured in hypoxia (sEVs-Hyp; n=10).

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Background: The American Heart Association recently published guidelines on how to clinically identify and categorize individuals with cardiovascular-kidney-metabolic (CKM) syndrome. The extent to which CKM syndrome prevalence and prognosis differ by sex remains unknown. This study aimed to examine the impact of sex on trends in prevalence over 30 years and the long-term prognosis of CKM syndrome in the United States.

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Looking Under the Hood at the Cytoskeletal Engine of Platelet Production.

Arterioscler Thromb Vasc Biol

December 2024

Vascular Biology Program, Boston Children's Hospital, MA (J.E.I., C.P., R.H.B.).

Blood platelets are anucleate cells essential for normal blood hemostasis. To maintain a normal platelet count of 150 000 to 400 000 per μL of blood, 10 platelets must be released each day from precursor cells called megakaryocytes. In this review, we aim to provide an overview of platelet production and evaluate the proposed mechanisms of platelet generation.

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Myocardial Hyperemia via Cardiomyocyte Catabolism of β-Hydroxybutyrate.

Arterioscler Thromb Vasc Biol

December 2024

Department of Medicine, Division of Environmental Medicine, Center for Cardiometabolic Science, University of Louisville, KY. (K.R.G., Y.N., N.C., E.B.S.-G., H.E.C., B.G.H., M.A.N.).

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DCBLD1 Modulates Angiogenesis by Regulation of the VEGFR-2 Endocytosis in Endothelial Cells.

Arterioscler Thromb Vasc Biol

December 2024

Department of Biochemistry and Molecular Biology, School of Basic Medicine, Hebei Medical University, Shijiazhuang, China. (Q.F., L.G., C.Y., X.L., Y.L., C.L., W.Z., Y.Z., W.Y., Y.M., R.W., L.L., Y.P., H.W., M.H., L.N.).

Background: Unwanted angiogenesis is involved in the progression of various malignant tumors and cardiovascular diseases, and the factors that regulate angiogenesis are potential therapeutic targets. We tested the hypothesis that DCBLD1 (discoidin, CUB, and LCCL domain-containing protein 1) is a coreceptor of VEGFR-2 (vascular endothelial growth factor receptor-2) and modulates angiogenesis in endothelial cells.

Methods: A carotid artery ligation model and retinal angiogenesis assay were used to study angiogenesis using globe knockout or endothelial cell-specific conditional knockout mice in vivo.

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Platelet-Specific Deletion of TGF-β1 Impairs Septic Thrombosis in Mice.

Arterioscler Thromb Vasc Biol

December 2024

Department of Hematology, Affiliated Hospital of Xuzhou Medical University, China. Blood Diseases Institute, Xuzhou Medical University, China. Key Laboratory of Bone Marrow Stem Cell, Xuzhou, China.

Article Synopsis
  • * The study used mouse models to analyze the effects of removing platelet-derived TGF-β1 during induced sepsis, measuring factors like survival time, platelet count, and immune cell recruitment.
  • * Results showed that TGF-β1 levels increased in the lungs during sepsis, and its deficiency improved survival and liver function, suggesting that targeting platelet-derived TGF-β1 could be a potential treatment strategy for sepsis.
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SGK1-Mediated Vascular Smooth Muscle Cell Phenotypic Transformation Promotes Thoracic Aortic Dissection Progression.

Arterioscler Thromb Vasc Biol

December 2024

Department of Cardiac Surgery, Central Hospital Affiliated to Shandong First Medical University, Jinan, China. (S.L., H.L., P.Z., Z.D., B.S., S.X., Y.N., X.T., L.Z., H.W., N.L., F.Z., W.Y.).

Background: The occurrence of thoracic aortic dissection (TAD) is closely related to the transformation of vascular smooth muscle cells (VSMCs) from a contractile to a synthetic phenotype. The role of SGK1 (serum- and glucocorticoid-regulated kinase 1) in VSMC phenotypic transformation and TAD occurrence is unclear.

Methods: Four-week-old male Sgk1 ( floxed) and Sgk1;Tagln (smooth muscle cell-specific knockout) mice were administered β-aminopropionitrile monofumarate for 4 weeks to model TAD.

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Circadian Dysfunction in the Skeletal Muscle Impairs Limb Perfusion and Muscle Regeneration in Peripheral Artery Disease.

Arterioscler Thromb Vasc Biol

December 2024

Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, IL. (P.Z., A.W.T.S., N.X.H., E.M.P., C.B.P.).

Article Synopsis
  • Peripheral artery disease (PAD) affects mobility due to reduced blood flow caused by atherosclerosis, and studies indicate that disruptions in circadian rhythms may impact vascular repair, particularly in limb ischemia situations.
  • This study explores the impact of the skeletal muscle circadian clock on adaptations to ischemic stress using a mouse model, focusing on the role of the circadian clock activator BMAL1 in muscle recovery after surgery-induced limb ischemia.
  • Findings revealed that circadian rhythm-related genes were altered in PAD patients, and the loss of BMAL1 in mice delayed muscle recovery post-ischemia, resulting in fewer regenerated muscle fibers and a decline in specific muscle fiber types.
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Long Noncoding RNA Function in Smooth Muscle Cell Plasticity and Atherosclerosis.

Arterioscler Thromb Vasc Biol

December 2024

Institute of Molecular Vascular Medicine, Klinikum rechts der Isar, Technical University Munich, Germany (L.M., F.F.).

Article Synopsis
  • * During vascular injury, signals from activated endothelial and inflammatory cells trigger SMCs to undergo phenotypic switching, allowing them to change into other cell types that contribute to atherosclerotic lesion development.
  • * Long noncoding RNAs have gained attention in atherosclerosis research for their role in regulating SMC identity, with advances in technology enabling precise study of their function and potential as therapeutic targets.
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Article Synopsis
  • Abdominal aortic aneurysm (AAA) is a major health issue with no effective medical treatments, so researchers are exploring IL-6 signaling inhibition as a potential therapy.
  • The study analyzed genetic data from large cohorts, finding strong associations between genetic variants linked to IL-6 signaling and reduced AAA risk.
  • The results suggest that targeting IL-6 signaling could be a viable approach for AAA treatment, though it may not be effective for other aneurysm types.
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Clinical and Genomic Prediction of Coronary Artery Disease Subtypes.

Arterioscler Thromb Vasc Biol

December 2024

Department of Genetics and Genomic Sciences, Icahn School of Medicine, New York, NY. (L.L., J.G.-G., H.M.W., C.J.H., P.F.O.R.).

Article Synopsis
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SR-BI Models for Spontaneous Myocardial Infarction: High Unesterified/Total Cholesterol Ratio Not the Sole Piece of the Puzzle.

Arterioscler Thromb Vasc Biol

December 2024

Division of Systems Pharmacology and Pharmacy, Leiden Academic Centre for Drug Research, Leiden University, the Netherlands. Pharmacy Leiden, the Netherlands.

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Tale of 2 Receptors.

Arterioscler Thromb Vasc Biol

November 2024

Center for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore. (D.K.S., J.M.C.).

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Disruption of PCSK9 Suppresses Inflammation and Attenuates Abdominal Aortic Aneurysm Formation.

Arterioscler Thromb Vasc Biol

November 2024

State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. (Z.P., H.C., H.R., Z.G., Q.W., J.Y., Y.Z., M.W.).

Article Synopsis
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Climate Change and Cardiovascular Disease: Who Is Vulnerable?

Arterioscler Thromb Vasc Biol

November 2024

Department of Environmental Health, Harvard T.H. Chan School of Public Health, Harvard University, Boston, MA (B.A.).

Climate change involves a shift in earth's climate indicators over extended periods of time due to human activity. Anthropogenic air pollution has resulted in trapping heat, contributing to global warming, which contributes to worsening air pollution through facilitating oxidizing of air constituents. It is becoming more evident that the effects of climate change, such as air pollution and ambient temperatures, are interconnected with each other and other environmental factors.

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Article Synopsis
  • Pharmacological inhibition of megalin in mice helps reduce atherosclerosis, but the study aimed to see if specifically deleting megalin in renal proximal tubule cells (PTCs) could have similar effects against hypercholesterolemia-induced atherosclerosis.
  • The experiments involved creating mice with and without megalin (PTC-LRP2 -/-) and inducing atherosclerosis by using a Western diet, but results showed that deleting megalin did not reduce atherosclerosis in any mice.
  • Instead, male PTC-LRP2 -/- mice exhibited severe kidney issues, including CD68+ cell infiltration and tubular atrophy, indicating that high-fat diets can lead to kidney damage independent of cholesterol levels, while female P
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Intravital Imaging of Disease Mechanisms in a Mouse Model of CCM Skin Lesions.

Arterioscler Thromb Vasc Biol

November 2024

Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Sweden (M.M.O., A.N., M.B.D., H.S., T.M., K.G.).

Background: Cerebral cavernous malformation (CCM) is a disease characterized by vascular malformations that primarily develop in the brain. These malformations are prone to leak, and their rupture or thrombotic closure can cause life-threatening hemorrhages and strokes. Mouse models have been instrumental to study the disease, but most cause premature lethality, precluding the investigation of disease mechanisms through intravital microscopy.

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Andexanet Alfa-Associated Heparin Resistance in Cardiac Surgery: Mechanism and In Vitro Perspectives.

Arterioscler Thromb Vasc Biol

November 2024

Division of Cardiothoracic Anesthesiology, Department of Anesthesiology and Critical Care, Perelman School of Medicine at the University of Pennsylvania, Philadelphia (L.K., N.K.T.).

Background: Andexanet alfa (andexanet) is the only Food and Drug Administration-approved antidote for direct FXa (factor Xa) inhibitors but has been reported to cause resistance to unfractionated heparin (UFH). This has delayed anticoagulation for procedures requiring cardiopulmonary bypass. The mechanism, andexanet and UFH dose dependence, and thrombotic risk of andexanet-associated heparin resistance are unknown.

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