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1. Full Text Neuropilin-1 mediates PDGF stimulation of vascular smooth muscle cell migration and signalling via p130Cas
by Pellet-Many, Caroline and Frankel, Paul and Evans, Ian M and Herzog, Birger and Jünemann-Ramírez, Manfred and Zachary, Ian C
Biochemical journal, ISSN 0264-6021, 05/2011, Volume 435, Issue 3, pp. 609 - 618
Platelet-derived growth factor (PDGF) | Glycosylation | Neuropilin-1 (NRP1) | Chemotaxis | p130 | Vascular endothelial growth factor (VEGF) | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Neuropilin-1 - genetics | Adenoviridae | Endothelial Cells | Neuropilin-1 - metabolism | Humans | Cells, Cultured | Crk-Associated Substrate Protein - metabolism | Muscle, Smooth, Vascular - cytology | Platelet-Derived Growth Factor - genetics | Crk-Associated Substrate Protein - genetics | Platelet-Derived Growth Factor - metabolism | Signal Transduction - physiology | Mutation | Myocytes, Smooth Muscle - cytology | Myocytes, Smooth Muscle - metabolism | Cell Movement | Index Medicus | HAoSMC, human aortic smooth muscle cell | Ad.NRP1ΔC, adenovirus expressing neuropilin-1 mutant lacking the intracellular domain | Cas, Crk-associated substrate | Ad.NRP1S612A, adenovirus expressing S612A mutant neuropilin-1 | PAE cell, porcine aortic endothelial cell | NRP1, neuropilin-1 | VEGFR2, VEGF receptor 2 | PDGFR, PDGF receptor | ERK, extracellular-signal-regulated kinase | NRP1 cell, PAE cell expressing NRP1 | HCASMC, human coronary artery smooth muscle cell | HCAEC, human coronary artery endothelial cell | HUVEC, human umbilical vein endothelial cell | chemotaxis | CS, chondroitin sulfate | GAPDH, glyceraldehyde-3-phosphate dehydrogenase | VSMC, vascular smooth muscle cell | FBS, fetal bovine serum | Ad.NRP1WT, adenovirus expressing wild-type neuropilin 1 | GAG, glycosaminoglycan | VEGF, vascular endothelial growth factor | glycosylation | vascular endothelial growth factor (VEGF) | p130Cas | platelet-derived growth factor (PDGF) | siRNA, small interfering RNA | HS, heparan sulfate | neuropilin-1 (NRP1) | PAE | Ad.GFP, adenovirus expressing green fluorescent protein | PDGF, platelet-derived growth factor
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2. Full Text An Unexpected Role of Semaphorin3A–Neuropilin-1 Signaling in Lymphatic Vessel Maturation and Valve Formation
by Jurisic, Giorgia and Maby-El Hajjami, Hélène and Karaman, Sinem and Ochsenbein, Alexandra M and Alitalo, Annamari and Siddiqui, Shoib S and Ochoa Pereira, Carlos and Petrova, Tatiana V and Detmar, Michael
Circulation research, ISSN 0009-7330, 08/2012, Volume 111, Issue 4, pp. 426 - 436
development | lymphatic valve | neuropilin-1 | lymphatic vessels | peri | microarrays | semaphorin 3A | Cardiac & Cardiovascular Systems | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Vertebrates: cardiovascular system | Neuropilin-1 - genetics | Antibodies, Neutralizing - administration & dosage | Oligonucleotide Array Sequence Analysis | Neuropilin-1 - metabolism | Humans | Vascular Endothelial Growth Factor A - metabolism | Semaphorin-3A - metabolism | Lymphatic Vessels - metabolism | Lymphangiogenesis | Myocytes, Smooth Muscle - metabolism | Neuropilin-1 - immunology | Semaphorin-3A - genetics | Lymphatic Vessels - embryology | Signal Transduction | Endothelial Cells - metabolism | Mice, Inbred C57BL | Pericytes - metabolism | Cells, Cultured | Gene Expression Profiling - methods | Cell Separation - methods | Gestational Age | Cell Lineage | Animals | Lymphatic Vessels - pathology | Mice | Cell Movement | Index Medicus | Neuropilin-1 | Lymphatic vessels | pericytes | Semaphorin 3A
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3. Full Text Neuropilin-1 facilitates SARS-CoV-2 cell entry and infectivity
by Cantuti-Castelvetri, Ludovico and Ojha, Ravi and Pedro, Liliana D and Djannatian, Minou and Franz, Jonas and Kuivanen, Suvi and van der Meer, Franziska and Kallio, Katri and Kaya, Tugberk and Anastasina, Maria and Smura, Teemu and Levanov, Lev and Szirovicza, Leonora and Tobi, Allan and Kallio-Kokko, Hannimari and Osterlund, Pamela and Joensuu, Merja and Meunier, Frederic A and Butcher, Sarah J and Winkler, Martin Sebastian and Mollenhauer, Brit and Helenius, Ari and Gokce, Ozgun and Teesalu, Tambet and Hepojoki, Jussi and Vapalahti, Olli and Stadelmann, Christine and Balistreri, Giuseppe and Simons, Mikael
Science (American Association for the Advancement of Science), ISSN 0036-8075, 11/2020, Volume 370, Issue 6518, pp. 856 - 860
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neuropilin-1 - genetics | Neuropilin-2 - metabolism | Pandemics | Neuropilin-1 - metabolism | Humans | Male | Olfactory Mucosa - metabolism | Virus Internalization | COVID-19 | Neuropilin-1 - chemistry | Peptidyl-Dipeptidase A - genetics | SARS-CoV-2 | Betacoronavirus - physiology | HEK293 Cells | Peptidyl-Dipeptidase A - metabolism | Serine Endopeptidases - genetics | Protein Domains | Female | Lung - metabolism | Host Microbial Interactions | Antibodies, Monoclonal - immunology | Neuropilin-1 - immunology | Caco-2 Cells | Peptide Fragments - metabolism | Spike Glycoprotein, Coronavirus - metabolism | Mice, Inbred C57BL | Olfactory Mucosa - virology | Angiotensin-Converting Enzyme 2 | Animals | Coronavirus Infections - virology | Protein Binding | Mice | Serine Endopeptidases - metabolism | Mutation | Respiratory Mucosa - metabolism | Betacoronavirus - genetics | Pneumonia, Viral - virology | Spike Glycoprotein, Coronavirus - chemistry | Metal Nanoparticles | Viral antibodies | Antiviral agents | Analysis | Severe acute respiratory syndrome | Antibodies | Coronaviruses | Health aspects | Tropism | Cell culture | Epithelial cells | Viral diseases | Blocking antibodies | Neuropilin | Viruses | Infections | Tissues | Angiotensin-converting enzyme 2--ACE2 | Cell surface | Cofactors | Proteins | Receptors | Peptidyl-dipeptidase A | Infectivity | Nose | Furin | Cleavage | Autopsies | Spike protein | Epithelium | Substrates | Severe acute respiratory syndrome coronavirus 2 | Disease transmission | Respiratory diseases | Angiotensin | Monoclonal antibodies | Olfactory epithelium | Cell migration | Viral infections | Index Medicus
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4. Full Text Neuropilin-1 is a host factor for SARS-CoV-2 infection
by Daly, James L and Simonetti, Boris and Klein, Katja and Chen, Kai-En and Williamson, Maia Kavanagh and Antón-Plágaro, Carlos and Shoemark, Deborah K and Simón-Gracia, Lorena and Bauer, Michael and Hollandi, Reka and Greber, Urs F and Horvath, Peter and Sessions, Richard B and Helenius, Ari and Hiscox, Julian A and Teesalu, Tambet and Matthews, David A and Davidson, Andrew D and Collins, Brett M and Cullen, Peter J and Yamauchi, Yohei
Science (American Association for the Advancement of Science), ISSN 0036-8075, 11/2020, Volume 370, Issue 6518, pp. 861 - 865
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neuropilin-1 - genetics | Pandemics | Neuropilin-1 - metabolism | Humans | Crystallography, X-Ray | Neuropilin-1 - antagonists & inhibitors | Virus Internalization | COVID-19 | Neuropilin-1 - chemistry | Peptidyl-Dipeptidase A - genetics | SARS-CoV-2 | RNA Interference | Betacoronavirus - physiology | Peptidyl-Dipeptidase A - metabolism | Protein Interaction Domains and Motifs | Antibodies, Monoclonal - immunology | Furin - metabolism | Caco-2 Cells | Peptide Fragments - metabolism | Mutagenesis, Site-Directed | Spike Glycoprotein, Coronavirus - genetics | Spike Glycoprotein, Coronavirus - metabolism | Amino Acid Motifs | Angiotensin-Converting Enzyme 2 | Peptide Fragments - chemistry | Coronavirus Infections - virology | Protein Binding | Antibodies, Monoclonal - metabolism | HeLa Cells | Pneumonia, Viral - virology | Spike Glycoprotein, Coronavirus - chemistry | Coronaviruses | Proteases | Health aspects | Biopolymers | Severe acute respiratory syndrome | Tropism | Cell culture | Epithelial cells | Proteinase | Viral diseases | Neuropilin | Viruses | Infections | Crystallography | Angiotensin-converting enzyme 2--ACE2 | Cell surface | X-ray crystallography | Proteins | Receptors | Peptidyl-dipeptidase A | Protease | Infectivity | Cell adhesion | Furin | Cleavage | Polypeptides | Spike protein | RNA-mediated interference | Glycoproteins | Epithelium | Substrates | Severe acute respiratory syndrome coronavirus 2 | Disease transmission | Respiratory diseases | Angiotensin | Monoclonal antibodies | Olfactory epithelium | Cell migration | Viral infections | Index Medicus
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5. Full Text Impeding Macrophage Entry into Hypoxic Tumor Areas by Sema3A/Nrp1 Signaling Blockade Inhibits Angiogenesis and Restores Antitumor Immunity
by Casazza, Andrea and Laoui, Damya and Wenes, Mathias and Rizzolio, Sabrina and Bassani, Nicklas and Mambretti, Marco and Deschoemaeker, Sofie and Van Ginderachter, Jo A and Tamagnone, Luca and Mazzone, Massimiliano
Cancer cell, ISSN 1535-6108, 12/2013, Volume 24, Issue 6, pp. 695 - 709
Oncology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Macrophages - physiology | Neuropilin-1 - genetics | Neuropilin-1 - antagonists & inhibitors | Mice, Knockout | Cell Hypoxia | Neoplasms, Experimental - pathology | Neuropilin-1 - physiology | Animals | Semaphorin-3A - physiology | Neoplasms, Experimental - immunology | Macrophages - drug effects | Neovascularization, Pathologic - prevention & control | Signal Transduction - physiology | Mice | Semaphorin-3A - antagonists & inhibitors | Neoplasms, Experimental - blood supply | Development and progression | Endothelial growth factors | Macrophages | Tumors | Index Medicus
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6. Full Text Neuropilin-1 mediates neutrophil elastase uptake and cross-presentation in breast cancer cells
by Kerros, Celine and Tripathi, Satyendra C and Zha, Dongxing and Mehrens, Jennifer M and Sergeeva, Anna and Philips, Anne V and Qiao, Na and Peters, Haley L and Katayama, Hiroyuki and Sukhumalchandra, Pariya and Ruisaard, Kathryn E and Perakis, Alexander A and St John, Lisa S and Lu, Sijie and Mittendorf, Elizabeth A and Clise-Dwyer, Karen and Herrmann, Amanda C and Alatrash, Gheath and Toniatti, Carlo and Hanash, Samir M and Ma, Qing and Molldrem, Jeffrey J
The Journal of biological chemistry, ISSN 0021-9258, 06/2017, Volume 292, Issue 24, pp. 10295 - 10305
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Leukocyte Elastase - metabolism | Neuropilin-1 - genetics | Antibodies, Blocking - metabolism | Breast Neoplasms - immunology | Neuropilin-1 - metabolism | Absorption, Physiological | Humans | Neoplasm Proteins - antagonists & inhibitors | Neoplasm Proteins - metabolism | Neuropilin-1 - antagonists & inhibitors | Breast Neoplasms - metabolism | Neuropilin-1 - chemistry | RNA Interference | Female | Protein Interaction Domains and Motifs | Neoplasm Proteins - genetics | Peptide Fragments - genetics | Recombinant Proteins - metabolism | T-Lymphocytes, Cytotoxic - immunology | Peptide Fragments - metabolism | Solubility | Recombinant Proteins - chemistry | Neoplasm Proteins - chemistry | Amino Acid Motifs | Peptide Fragments - chemistry | Leukocyte Elastase - chemistry | T-Lymphocytes, Cytotoxic - metabolism | Breast Neoplasms - pathology | CRISPR-Cas Systems | Cell Line, Tumor | Cross-Priming | Ligands | Kinetics | Leukocyte Elastase - immunology | Index Medicus | antigen presentation | cross-presentation | receptor internalization | neutrophil elastase | immunotherapy | neuropilin-1 | breast cancer | serine protease | Cell Biology
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7. Full Text Neuropilin 1 deficiency on CD4+Foxp3+ regulatory T cells impairs mouse melanoma growth
by Hansen, Wiebke and Hutzler, Marina and Abel, Simone and Alter, Christina and Stockmann, Christian and Kliche, Stefanie and Albert, Juliane and Sparwasser, Tim and Sakaguchi, Shimon and Westendorf, Astrid M and Schadendorf, Dirk and Buer, Jan and Helfrich, Iris
The Journal of experimental medicine, ISSN 0022-1007, 10/2012, Volume 209, Issue 11, pp. 2001 - 2016
Immunology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Forkhead Transcription Factors - immunology | Immunohistochemistry | Neuropilin-1 - genetics | T-Lymphocytes, Regulatory - metabolism | Vascular Endothelial Growth Factor A - deficiency | Tumor Escape - genetics | Humans | Gene Expression Regulation, Neoplastic | Melanoma, Experimental - metabolism | Vascular Endothelial Growth Factor A - genetics | Cell Movement - genetics | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | Cell Movement - immunology | Lymphocyte Activation - immunology | Flow Cytometry | Melanoma, Experimental - immunology | Forkhead Transcription Factors - metabolism | CD8-Positive T-Lymphocytes - metabolism | Tumor Burden - genetics | Neuropilin-1 - immunology | Tumor Escape - immunology | Skin Neoplasms - immunology | Mice, Inbred C57BL | CD4-Positive T-Lymphocytes - metabolism | Mice, Transgenic | Vascular Endothelial Growth Factor A - immunology | Reverse Transcriptase Polymerase Chain Reaction | Mice, Knockout | Skin Neoplasms - metabolism | Animals | Melanoma, Experimental - genetics | Skin Neoplasms - genetics | Cell Line, Tumor | Mice | CD8-Positive T-Lymphocytes - immunology | Neuropilin-1 - deficiency | Tumor Burden - immunology | Index Medicus
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8. Full Text Neuropilin-1 distinguishes natural and inducible regulatory T cells among regulatory T cell subsets in vivo
by Yadav, Mahesh and Louvet, Cedric and Davini, Dan and Gardner, James M and Martinez-Llordella, Marc and Bailey-Bucktrout, Samantha and Anthony, Bryan A and Sverdrup, Francis M and Head, Richard and Kuster, Daniel J and Ruminski, Peter and Weiss, David and Von Schack, David and Bluestone, Jeffrey A
The Journal of experimental medicine, ISSN 0022-1007, 09/2012, Volume 209, Issue 10, pp. 1713 - 1722
Immunology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Autoimmunity | Neuropilin-1 - genetics | T-Lymphocyte Subsets - immunology | T-Lymphocytes, Regulatory - metabolism | Myelin Basic Protein - metabolism | Receptors, Antigen, T-Cell - metabolism | Neuropilin-1 - metabolism | Mice, Inbred C57BL | Gene Expression Regulation | Lymphoid Tissue - metabolism | Male | Mice, Transgenic | Lymphoid Tissue - immunology | T-Lymphocytes, Regulatory - immunology | Myelin Basic Protein - genetics | Lymphocyte Activation - genetics | Animals | T-Lymphocyte Subsets - metabolism | Mice, Inbred NOD | Mice | Receptors, Antigen, T-Cell - genetics | Index Medicus | Brief Definitive Report
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9. Full Text Neuropilin 1 is expressed on thymus-derived natural regulatory T cells, but not mucosa- generated induced Foxp3(+) T reg cells
by Weiss, Jonathan M and Bilate, Angelina M and Gobert, Michael and Ding, Yi and de Lafaille, Maria A. Curotto and Parkhurst, Christopher N and Xiong, Huizhong and Dolpady, Jayashree and Frey, Alan B and Ruocco, Maria Grazia and Yang, Yi and Floess, Stefan and Huehn, Jochen and Oh, Soyoung and Li, Ming O and Niec, Rachel E and Rudensky, Alexander Y and Dustin, Michael L and Littman, Dan R and Lafaille, Juan J
The Journal of experimental medicine, ISSN 0022-1007, 09/2012, Volume 209, Issue 10, pp. 1723 - 1742
Immunology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Neuropilin-1 - genetics | T-Lymphocytes, Regulatory - metabolism | Neuropilin-1 - metabolism | Intestines - metabolism | Intestines - immunology | T-Lymphocytes, Regulatory - immunology | Inflammation - metabolism | Lymphocyte Activation - immunology | Forkhead Transcription Factors - metabolism | Lymphocytes, Tumor-Infiltrating - metabolism | Cell Membrane - metabolism | Thymus Gland - metabolism | Mice, Transgenic | Inflammation - immunology | Mucous Membrane - metabolism | Gene Expression Regulation - drug effects | Cell Lineage | Transforming Growth Factor beta - pharmacology | Animals | Intestines - microbiology | Mucous Membrane - immunology | Thymus Gland - immunology | Mice | Metagenome - immunology | Lymphocytes, Tumor-Infiltrating - immunology | Index Medicus
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