The functional role of soluble proteins acquired by extracellular vesicles
暂无分享,去创建一个
P. Ciancaglini | J. Millán | N. Rosato | M. Bottini | R. Buchet | S. Mebarek | A. Ramos | H. G. Sebinelli
[1] Demao Zhang,et al. Matrix Vesicles as a Therapeutic Target for Vascular Calcification , 2022, Frontiers in Cell and Developmental Biology.
[2] T. Hope,et al. Circulating ACE2-expressing extracellular vesicles block broad strains of SARS-CoV-2 , 2022, Nature communications.
[3] Meiwan Chen,et al. The impact of protein corona on the biological behavior of targeting nanomedicines. , 2022, International journal of pharmaceutics.
[4] V. Novakovic,et al. The Central Role of Extracellular Vesicles in the Mechanisms of Thrombosis in COVID-19 Patients With Cancer and Therapeutic Strategies , 2022, Frontiers in Cell and Developmental Biology.
[5] M. Pfaffl,et al. Extracellular Vesicle Associated miRNAs Regulate Signaling Pathways Involved in COVID-19 Pneumonia and the Progression to Severe Acute Respiratory Corona Virus-2 Syndrome , 2021, Frontiers in Immunology.
[6] P. Mozdziak,et al. Small Extracellular Vesicles and COVID19—Using the “Trojan Horse” to Tackle the Giant , 2021, Cells.
[7] Á. Kittel,et al. Formation of a protein corona on the surface of extracellular vesicles in blood plasma , 2021, Journal of extracellular vesicles.
[8] S. Perlman,et al. Innate immune and inflammatory responses to SARS-CoV-2: Implications for COVID-19 , 2021, Cell Host & Microbe.
[9] G. Melli,et al. Circulating extracellular vesicles are endowed with enhanced procoagulant activity in SARS-CoV-2 infection , 2021, EBioMedicine.
[10] G. Jiang,et al. Inherited and acquired corona of coronavirus in the host: Inspiration from the biomolecular corona of nanoparticles , 2021, Nano Today.
[11] M. Brizzi,et al. Extracellular Vesicles Tune the Immune System in Renal Disease: A Focus on Systemic Lupus Erythematosus, Antiphospholipid Syndrome, Thrombotic Microangiopathy and ANCA-Vasculitis , 2021, International journal of molecular sciences.
[12] G. Randall,et al. A novel soluble ACE2 protein totally protects from lethal disease caused by SARS-CoV-2 infection , 2021, bioRxiv.
[13] J. Thachil,et al. Managing thrombosis and cardiovascular complications of COVID-19: answering the questions in COVID-19-associated coagulopathy , 2021, Expert review of respiratory medicine.
[14] G. Cappellano,et al. Circulating Exosomes Are Strongly Involved in SARS-CoV-2 Infection , 2021, Frontiers in Molecular Biosciences.
[15] Jaesung Park,et al. Single‐vesicle imaging and co‐localization analysis for tetraspanin profiling of individual extracellular vesicles , 2021, Journal of extracellular vesicles.
[16] A. Bukatin,et al. Biomechanical Properties of Blood Plasma Extracellular Vesicles Revealed by Atomic Force Microscopy , 2020, Biology.
[17] L. Martin-Jaular,et al. Extracellular vesicles containing ACE2 efficiently prevent infection by SARS‐CoV‐2 Spike protein‐containing virus , 2020, Journal of extracellular vesicles.
[18] R. Coffey,et al. Angiotensin-converting Enzyme 2–containing Small Extracellular Vesicles and Exomeres Bind the Severe Acute Respiratory Syndrome Coronavirus 2 Spike Protein , 2020, Gastroenterology.
[19] Amber L. Simpson,et al. Extracellular Vesicle and Particle Biomarkers Define Multiple Human Cancers , 2020, Cell.
[20] K. Landfester,et al. Preparation of the Protein Corona: How Washing Shapes the Proteome and Influences Cellular Uptake of Nanocarriers. , 2020, Acta biomaterialia.
[21] P. Ciancaglini,et al. Lipid composition modulates ATP hydrolysis and calcium phosphate mineral propagation by TNAP-harboring proteoliposomes. , 2020, Archives of biochemistry and biophysics.
[22] J. Gebert,et al. Inter-Laboratory Comparison of Extracellular Vesicle Isolation Based on Ultracentrifugation , 2020, Transfusion Medicine and Hemotherapy.
[23] T. Rakshit,et al. Identification of Biomarker Hyaluronan on Colon Cancer Extracellular Vesicles Using Correlative AFM and Spectroscopy. , 2020, The journal of physical chemistry letters.
[24] M. Nouri,et al. The role of extracellular vesicles in COVID-19 virus infection , 2020, Infection, Genetics and Evolution.
[25] Y. Yoshiko,et al. Emerging roles of microRNAs as extracellular vesicle cargo secreted from osteoblasts. , 2020, Journal of oral biosciences.
[26] G. Caracciolo,et al. Personalized Graphene Oxide-Protein Corona in the Human Plasma of Pancreatic Cancer Patients , 2020, Frontiers in Bioengineering and Biotechnology.
[27] Z. Percario,et al. The Role of Extracellular Vesicles as Allies of HIV, HCV and SARS Viruses , 2020, Viruses.
[28] P. Ciancaglini,et al. Matrix vesicle biomimetics harboring Annexin A5 and alkaline phosphatase bind to the native collagen matrix produced by mineralizing vascular smooth muscle cells. , 2020, Biochimica et biophysica acta. General subjects.
[29] Martin Stahl,et al. Inhibition of SARS-CoV-2 Infections in Engineered Human Tissues Using Clinical-Grade Soluble Human ACE2 , 2020, Cell.
[30] M. Gimona,et al. Differential fluorescence nanoparticle tracking analysis for enumeration of the extracellular vesicle content in mixed particulate solutions. , 2020, Methods.
[31] H. Yoshioka,et al. The matrix vesicle cargo miR-125b accumulates in the bone matrix, inhibiting bone resorption in mice , 2020, Communications Biology.
[32] P. Pagès,et al. Monitoring HSP70 exosomes in cancer patients’ follow up: a clinical prospective pilot study , 2020, Journal of extracellular vesicles.
[33] Gareth R. Williams,et al. Acoustic Immunosensing of Exosomes Using a Quartz Crystal Microbalance with Dissipation Monitoring , 2019, Analytical chemistry.
[34] P. Ciancaglini,et al. Cholesterol regulates the incorporation and catalytic activity of tissue-nonspecific alkaline phosphatase in DPPC monolayers. , 2019, Langmuir : the ACS journal of surfaces and colloids.
[35] V. Macrae,et al. Differing calcification processes in cultured vascular smooth muscle cells and osteoblasts , 2019, Experimental cell research.
[36] K. Kang,et al. Phosphatidylserine receptor-targeting therapies for the treatment of cancer , 2019, Archives of pharmacal research.
[37] S. Esener,et al. Quantitative atomic force microscopy provides new insight into matrix vesicle mineralization. , 2019, Archives of biochemistry and biophysics.
[38] R. Krittayaphong,et al. Altered profile of circulating microparticles in nonvalvular atrial fibrillation , 2019, Clinical cardiology.
[39] M. Yáñez-Mó,et al. High sensitivity detection of extracellular vesicles immune-captured from urine by conventional flow cytometry , 2019, Scientific Reports.
[40] G. Jenster,et al. Extracellular Vesicle Quantification and Characterization: Common Methods and Emerging Approaches , 2019, Bioengineering.
[41] E. Aikawa,et al. Roles and Regulation of Extracellular Vesicles in Cardiovascular Mineral Metabolism , 2018, Front. Cardiovasc. Med..
[42] Jing Xu,et al. Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines , 2018, Journal of Extracellular Vesicles.
[43] P. Ciancaglini,et al. Lipid microenvironment affects the ability of proteoliposomes harboring TNAP to induce mineralization without nucleators , 2018, Journal of Bone and Mineral Metabolism.
[44] Samer M. Al-Hakami,et al. Membrane Proteins Significantly Restrict Exosome Mobility , 2017, bioRxiv.
[45] E. Buzás,et al. Molecular interactions at the surface of extracellular vesicles , 2018, Seminars in Immunopathology.
[46] R. Koenen,et al. Initiation and Propagation of Vascular Calcification Is Regulated by a Concert of Platelet- and Smooth Muscle Cell-Derived Extracellular Vesicles , 2018, Front. Cardiovasc. Med..
[47] A. Durham,et al. Role of smooth muscle cells in vascular calcification: implications in atherosclerosis and arterial stiffness , 2018, Cardiovascular research.
[48] P. Ciancaglini,et al. Matrix vesicles from chondrocytes and osteoblasts: Their biogenesis, properties, functions and biomimetic models. , 2018, Biochimica et biophysica acta. General subjects.
[49] G. Pasquinelli,et al. Mechanisms of Arterial Calcification: The Role of Matrix Vesicles. , 2018, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery.
[50] P. Laktionov,et al. Isolation of Extracellular Vesicles: General Methodologies and Latest Trends , 2018, BioMed research international.
[51] N. Chen,et al. Matrix vesicles induce calcification of recipient vascular smooth muscle cells through multiple signaling pathways. , 2017, Kidney international.
[52] Joshua D. Hutcheson,et al. Extracellular Vesicles As Mediators of Cardiovascular Calcification , 2017, Front. Cardiovasc. Med..
[53] Krisztina V. Vukman,et al. Antibiotic-induced release of small extracellular vesicles (exosomes) with surface-associated DNA , 2017, Scientific Reports.
[54] D. Ricard,et al. Glioblastoma stem-like cells secrete the pro-angiogenic VEGF-A factor in extracellular vesicles , 2017, Journal of extracellular vesicles.
[55] E. Buzás,et al. Monocyte activation drives preservation of membrane thiols by promoting release of oxidised membrane moieties via extracellular vesicles , 2017, Free radical biology & medicine.
[56] R. Brekken,et al. Detection of phosphatidylserine-positive exosomes for the diagnosis of early-stage malignancies , 2017, British Journal of Cancer.
[57] M. Dweck,et al. End stage renal disease‐induced hypercalcemia may promote aortic valve calcification via Annexin VI enrichment of valve interstitial cell derived‐matrix vesicles , 2017, Journal of cellular physiology.
[58] C. Gerber,et al. Imaging modes of atomic force microscopy for application in molecular and cell biology. , 2017, Nature nanotechnology.
[59] P. Meikle,et al. Transitional changes in the CRP structure lead to the exposure of proinflammatory binding sites , 2017, Nature Communications.
[60] E. Noulsri,et al. Microparticles from splenectomized β-thalassemia/HbE patients play roles on procoagulant activities with thrombotic potential , 2017, Annals of Hematology.
[61] J. Lötvall,et al. Detailed Analysis of Protein Topology of Extracellular Vesicles–Evidence of Unconventional Membrane Protein Orientation , 2016, Scientific Reports.
[62] Andreas B. Dahlin,et al. Dual-Wavelength Surface Plasmon Resonance for Determining the Size and Concentration of Sub-Populations of Extracellular Vesicles. , 2016, Analytical chemistry.
[63] Yiping Cui,et al. Imaging and Intracellular Tracking of Cancer-Derived Exosomes Using Single-Molecule Localization-Based Super-Resolution Microscope. , 2016, ACS applied materials & interfaces.
[64] P. Fortin,et al. Distinct Subtypes of Microparticle-containing Immune Complexes Are Associated with Disease Activity, Damage, and Carotid Intima-media Thickness in Systemic Lupus Erythematosus , 2016, The Journal of Rheumatology.
[65] B. Boyan,et al. Selective enrichment of microRNAs in extracellular matrix vesicles produced by growth plate chondrocytes. , 2016, Bone.
[66] C. Théry,et al. Proteomic comparison defines novel markers to characterize heterogeneous populations of extracellular vesicle subtypes , 2016, Proceedings of the National Academy of Sciences.
[67] W. Landis,et al. Matrix vesicles: Are they anchored exosomes? , 2015, Bone.
[68] N. Chen,et al. Pathophysiology of Vascular Calcification , 2015, Current Osteoporosis Reports.
[69] S. Janga,et al. Differential miRNA Expression in Cells and Matrix Vesicles in Vascular Smooth Muscle Cells from Rats with Kidney Disease , 2015, PloS one.
[70] Alissa M. Weaver,et al. Directional cell movement through tissues is controlled by exosome secretion , 2015, Nature Communications.
[71] P. Ghezzi,et al. Cysteine Oxidation Targets Peroxiredoxins 1 and 2 for Exosomal Release through a Novel Mechanism of Redox-Dependent Secretion , 2015, Molecular medicine.
[72] K. Davies,et al. The TAM family: phosphatidylserine-sensing receptor tyrosine kinases gone awry in cancer , 2014, Nature Reviews Cancer.
[73] Sanjeev Palta,et al. Overview of the coagulation system , 2014, Indian journal of anaesthesia.
[74] A. Falus,et al. Emerging role of extracellular vesicles in inflammatory diseases , 2014, Nature Reviews Rheumatology.
[75] P. Robbins,et al. Regulation of immune responses by extracellular vesicles , 2014, Nature Reviews Immunology.
[76] Andrew F. Hill,et al. Minimal experimental requirements for definition of extracellular vesicles and their functions: a position statement from the International Society for Extracellular Vesicles , 2014, Journal of extracellular vesicles.
[77] S. Stanworth,et al. Levels of procoagulant microvesicles are elevated after traumatic injury and platelet microvesicles are negatively correlated with mortality , 2014, Journal of extracellular vesicles.
[78] Ian N Bruce,et al. Suppression of inflammation reduces endothelial microparticles in active systemic lupus erythematosus , 2013, Annals of the rheumatic diseases.
[79] Yvan Campos,et al. Identification and characterization of the nano‐sized vesicles released by muscle cells , 2013, FEBS letters.
[80] Imre Mäger,et al. Extracellular vesicles: biology and emerging therapeutic opportunities , 2013, Nature Reviews Drug Discovery.
[81] Nunzio Bottini,et al. Surface polyethylene glycol conformation influences the protein corona of polyethylene glycol-modified single-walled carbon nanotubes: potential implications on biological performance. , 2013, ACS nano.
[82] Roopashree Subbaiah,et al. The exposure of autoantigens by microparticles underlies the formation of potent inflammatory components: the microparticle-associated immune complexes , 2012, EMBO molecular medicine.
[83] J. Millán. The Role of Phosphatases in the Initiation of Skeletal Mineralization , 2012, Calcified Tissue International.
[84] S. Reed,et al. Membrane curvature recognition by C-reactive protein using lipoprotein mimics. , 2012, Soft matter.
[85] L. Truedsson,et al. Increased IgG on cell-derived plasma microparticles in systemic lupus erythematosus is associated with autoantibodies and complement activation. , 2012, Arthritis and rheumatism.
[86] J. Gimzewski,et al. Quantitative nanostructural and single-molecule force spectroscopy biomolecular analysis of human-saliva-derived exosomes. , 2011, Langmuir : the ACS journal of surfaces and colloids.
[87] K. Midwood,et al. Plasma and cellular fibronectin: distinct and independent functions during tissue repair , 2011, Fibrogenesis & tissue repair.
[88] M. Dadlez,et al. Proteomic characterization of biogenesis and functions of matrix vesicles released from mineralizing human osteoblast-like cells. , 2011, Journal of proteomics.
[89] H. Kubo,et al. Receptor for advanced glycation end products binds to phosphatidylserine and assists in the clearance of apoptotic cells , 2011, EMBO reports.
[90] Anikó Szalai,et al. Detection and isolation of cell-derived microparticles are compromised by protein complexes resulting from shared biophysical parameters. , 2011, Blood.
[91] John D Lambris,et al. Molecular Intercommunication between the Complement and Coagulation Systems , 2010, The Journal of Immunology.
[92] J. Schwarzbauer,et al. Assembly of fibronectin extracellular matrix. , 2010, Annual review of cell and developmental biology.
[93] N. Chen,et al. RhoA/Rho kinase (ROCK) alters fetuin-A uptake and regulates calcification in bovine vascular smooth muscle cells (BVSMC). , 2010, American journal of physiology. Renal physiology.
[94] Wen-chao Song,et al. Complement and its role in innate and adaptive immune responses , 2010, Cell Research.
[95] M. Tso,et al. Autophagy and Exosomes in the Aged Retinal Pigment Epithelium: Possible Relevance to Drusen Formation and Age-Related Macular Degeneration , 2009, PloS one.
[96] N. Chen,et al. Annexin‐Mediated Matrix Vesicle Calcification in Vascular Smooth Muscle Cells , 2008, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[97] B. Lentz,et al. A phosphatidylserine binding site in factor Va C1 domain regulates both assembly and activity of the prothrombinase complex. , 2008, Blood.
[98] Simon C Watkins,et al. Exosomes As a Short-Range Mechanism to Spread Alloantigen between Dendritic Cells during T Cell Allorecognition1 , 2008, The Journal of Immunology.
[99] Tony Yeung,et al. Membrane Phosphatidylserine Regulates Surface Charge and Protein Localization , 2008, Science.
[100] T. Kwon,et al. Rapid cell corpse clearance by stabilin-2, a membrane phosphatidylserine receptor , 2008, Cell Death and Differentiation.
[101] G. Freeman,et al. TIM-1 and TIM-4 glycoproteins bind phosphatidylserine and mediate uptake of apoptotic cells. , 2007, Immunity.
[102] Michael R. Elliott,et al. BAI1 is an engulfment receptor for apoptotic cells upstream of the ELMO/Dock180/Rac module , 2007, Nature.
[103] John D Lambris,et al. Generation of C5a in the absence of C3: a new complement activation pathway , 2006, Nature Medicine.
[104] C. Théry,et al. Accumulation of MFG-E8/lactadherin on exosomes from immature dendritic cells. , 2005, Blood cells, molecules & diseases.
[105] C. Théry,et al. ICAM-1 on exosomes from mature dendritic cells is critical for efficient naive T-cell priming. , 2005, Blood.
[106] G. Multhoff,et al. Immunostimulatory functions of membrane-bound and exported heat shock protein 70. , 2005, Exercise immunology review.
[107] Simon C Watkins,et al. Endocytosis, intracellular sorting, and processing of exosomes by dendritic cells. , 2004, Blood.
[108] P. Ghezzi,et al. Redox regulation of surface protein thiols: Identification of integrin α-4 as a molecular target by using redox proteomics , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[109] R. Hebbel,et al. Sickle blood contains tissue factor-positive microparticles derived from endothelial cells and monocytes. , 2003, Blood.
[110] Aled Clayton,et al. Antigen‐presenting cell exosomes are protected from complement‐mediated lysis by expression of CD55 and CD59 , 2003, European journal of immunology.
[111] Keiko Miwa,et al. Identification of a factor that links apoptotic cells to phagocytes , 2002, Nature.
[112] N. Aoki,et al. Secretion of a peripheral membrane protein, MFG-E8, as a complex with membrane vesicles. , 2002, European journal of biochemistry.
[113] J. Volanakis,et al. Topology and Structure of the C1q-Binding Site on C-Reactive Protein1 , 2001, The Journal of Immunology.
[114] N. Brot,et al. C-Reactive Protein Binds to Apoptotic Cells, Protects the Cells from Assembly of the Terminal Complement Components, and Sustains an Antiinflammatory Innate Immune Response , 2000, The Journal of experimental medicine.
[115] M. Vidal,et al. Exosomes released during reticulocyte maturation bind to fibronectin via integrin α4β1 , 2000 .
[116] J. Freyssinet,et al. Monocyte vesiculation is a possible mechanism for dissemination of membrane-associated procoagulant activities and adhesion molecules after stimulation by lipopolysaccharide. , 1994, Journal of immunology.
[117] J. Luzio,et al. Ectocytosis caused by sublytic autologous complement attack on human neutrophils. The sorting of endogenous plasma-membrane proteins and lipids into shed vesicles. , 1991, The Biochemical journal.
[118] T. Drake,et al. Selective cellular expression of tissue factor in human tissues. Implications for disorders of hemostasis and thrombosis. , 1989, The American journal of pathology.
[119] H. Anderson,et al. Matrix Vesicles in Atherosclerotic Calcification 1 , 1983, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.