Michael L. Dustin

ORCID: 0000-0003-4983-6389
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About
Contact & Profiles
Research Areas
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • Cell Adhesion Molecules Research
  • CAR-T cell therapy research
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Immunotherapy and Biomarkers
  • Immune Response and Inflammation
  • Immune cells in cancer
  • Cellular Mechanics and Interactions
  • Lipid Membrane Structure and Behavior
  • Single-cell and spatial transcriptomics
  • HIV Research and Treatment
  • Chemokine receptors and signaling
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Nanofabrication and Lithography Techniques
  • Cytomegalovirus and herpesvirus research
  • Atherosclerosis and Cardiovascular Diseases
  • Advanced Fluorescence Microscopy Techniques
  • RNA Interference and Gene Delivery
  • Pancreatic and Hepatic Oncology Research
  • interferon and immune responses
  • Immunodeficiency and Autoimmune Disorders
  • Cell Image Analysis Techniques
  • Diabetes and associated disorders

University of Oxford
2016-2025

Nuffield Orthopaedic Centre
2015-2025

Chinese Academy of Medical Sciences & Peking Union Medical College
2025

New York University
2013-2024

Kennedy Center
2015-2024

Institute of Rheumatology
2015-2024

RELX Group (United States)
2023-2024

Science Oxford
2023

University of California, San Francisco
1988-2023

University of Freiburg
2023

The specialized junction between a T lymphocyte and an antigen-presenting cell, the immunological synapse, consists of central cluster cell receptors surrounded by ring adhesion molecules. Immunological synapse formation is now shown to be active dynamic mechanism that allows cells distinguish potential antigenic ligands. Initially, receptor ligands were engaged in outermost nascent synapse. Transport these complexes into was dependent on receptor–ligand interaction kinetics. Finally, stable...

10.1126/science.285.5425.221 article EN Science 1999-07-09

Abstract ICAM-1 is a cell surface glycoprotein originally defined by monoclonal antibody (MAb) that inhibits phorbol ester-stimulated leukocyte aggregation. Staining of frozen sections and immunofluorescence flow cytometry showed intercellular adhesion molecule-1 (ICAM-1) expressed on non-hematopoietic cells such as vascular endothelial cells, thymic epithelial certain other fibroblasts, hematopoietic tissue macrophages, mitogen-stimulated T lymphocyte blasts, germinal center dendritic in...

10.4049/jimmunol.137.1.245 article EN The Journal of Immunology 1986-07-01

Homotypic adhesion by phorbol ester-stimulated lymphocytes requires LFA-1 and Mg+2 does not involve like-like interactions between molecules on adjacent cells. The latter finding suggested that a second molecule, distinct from LFA-1, also participates in LFA-1-dependent adhesion. identification of such molecule was the object this investigation. After immunization with LFA-1-deficient EBV-transformed lymphoblastoid cells, MAb obtained inhibits aggregation LFA-1+ EBV lines. This defines novel...

10.4049/jimmunol.137.4.1270 article EN The Journal of Immunology 1986-08-15

Intercellular adhesion molecule-1 (ICAM-1) on the surface of cultured umbilical vein and saphenous endothelial cells was upregulated between 2.5- 40-fold by rIL-1, rTNF, LPS rIFN gamma corresponding to up 5 X 10(6) sites/cell. Endothelial cell ICAM-1 a single band 90 kD in SDS-PAGE. Purified reconstituted into liposomes bound plastic an excellent substrate for both JY B lymphoblastoid T lymphoblast adhesion. Adhesion planar membranes blocked completely monoclonal antibodies lymphocyte...

10.1083/jcb.107.1.321 article EN The Journal of Cell Biology 1988-07-01
Andrea Cossarizza Hyun‐Dong Chang Andreas Radbruch Andreas Acs Dieter Adam and 95 more Sabine Adam‐Klages William W. Agace Nima Aghaeepour Mübeccel Akdiş Matthieu Allez Larissa Nogueira Almeida Giorgia Alvisi Graham Anderson Immanuel Andrä Francesco Annunziato Achille Anselmo Petra Bächer Cosima T. Baldari Sudipto Bari Vincenzo Barnaba Joana Barros‐Martins Luca Battistini Wolfgang Bauer Sabine Baumgart Nicole Baumgarth Dirk Baumjohann Bianka Baying Mary Bebawy Burkhard Becher Wolfgang Beisker Vladimı́r Beneš Rudi Beyaert Alfonso Blanco Dominic A. Boardman Christian Bogdan Jessica G Borger Giovanna Borsellino Philip E. Boulais Jolene A. Bradford Dirk Brenner Ryan R. Brinkman Anna E. S. Brooks Dirk H. Busch Martin Büscher Timothy Bushnell Federica Calzetti Garth Cameron Ilenia Cammarata Xuetao Cao Susanna Cardell Stefano Casola Marco A. Cassatella Andrea Cavani Antonio Celada Lucienne Chatenoud Pratip K. Chattopadhyay Sue Chow Eleni Christakou Luka Čičin‐Šain Mario Clerici Federico Colombo Laura Cook Anne Cooke Andrea M. Cooper Alexandra J. Corbett Antonio Cosma Lorenzo Cosmi Pierre G. Coulie Ana Cumano Ljiljana Cvetkovic Van Duc Dang Chantip Dang‐Heine Martin S. Davey Derek Davies Sara De Biasi Genny Del Zotto Gelo Victoriano Dela Cruz Michael Delacher Silvia Della Bella Paolo Dellabona Günnur Deniz Mark C. Dessing James P. Di Santo Andreas Diefenbach Francesco Dieli Andreas Dolf Thomas Dörner Regine J. Dress Diana Dudziak Michael L. Dustin Charles‐Antoine Dutertre Friederike Ebner Sidonia B. G. Eckle Matthias Edinger Pascale Eede Götz R. A. Ehrhardt Marcus Eich Pablo Engel Britta Engelhardt Anna Erdei

These guidelines are a consensus work of considerable number members the immunology and flow cytometry community. They provide theory key practical aspects enabling immunologists to avoid common errors that often undermine immunological data. Notably, there comprehensive sections all major immune cell types with helpful Tables detailing phenotypes in murine human cells. The latest techniques applications also described, featuring examples data can be generated and, importantly, how analysed....

10.1002/eji.201970107 article EN European Journal of Immunology 2019-10-01

CD2-associated protein (CD2AP) is an 80-kilodalton that critical for stabilizing contacts between T cells and antigen-presenting cells. In CD2AP-deficient mice, immune function was compromised, but the mice died at 6 to 7 weeks of age from renal failure. kidney, CD2AP expressed primarily in glomerular epithelial Knockout exhibited defects cell foot processes, accompanied by mesangial hyperplasia extracellular matrix deposition. Supporting a role specialized junction known as slit diaphragm,...

10.1126/science.286.5438.312 article EN Science 1999-10-08

The area of contact between a T cell and an antigen-presenting (APC) is known as the immunological synapse. Although its exact function unknown, one model suggests that it allows for receptor (TCR) clustering sustained signaling in cells many hours. Here we demonstrate TCR-mediated tyrosine kinase naı̈ve occurred primarily at periphery synapse was largely abated before mature synapses had formed. These data suggest hours TCR are not required activation. observations challenge current ideas about role

10.1126/science.1067710 article EN Science 2002-02-22

The growth factor progranulin (PGRN) has been implicated in embryonic development, tissue repair, tumorigenesis, and inflammation, but its receptors remain unidentified. We report that PGRN bound directly to tumor necrosis (TNFRs) disturbed the TNFα-TNFR interaction. PGRN-deficient mice were susceptible collagen-induced arthritis, administration of reversed inflammatory arthritis. Atsttrin, an engineered protein composed three fragments, exhibited selective TNFR binding. Atsttrin prevented...

10.1126/science.1199214 article EN Science 2011-03-11

The cell surface expression and function of the LFA-1 ligand, intercellular adhesion molecule 1 (ICAM-1), on epidermal keratinocytes (EK) was studied. ICAM-1 cultured EK either absent or weak, but induced by treating with rIFN-gamma TNF for 4-48 h. IFN-gamma were synergistic. treatment increased T lymphoblast from less than 2% to 20-40%, a concentration dependence similar that seen induction. All inhibited mAbs, not HLA-DR, CD2, LFA-3 mAbs. There no difference in level IFN-gamma-treated...

10.1084/jem.167.4.1323 article EN The Journal of Experimental Medicine 1988-04-01

Abstract Recruitment of effector T cells to inflamed peripheral tissues is regulated by chemokines and their receptors, but the factors regulating recruitment tumors remain largely undefined. Ionizing radiation (IR) therapy a common treatment modality for breast other cancers. Used as cytocidal agent proliferating cancer cells, IR in combination with immunotherapy has been shown promote immune-mediated tumor destruction preclinical studies. In this study we demonstrate that markedly enhanced...

10.4049/jimmunol.181.5.3099 article EN The Journal of Immunology 2008-09-01

We examined the in vivo behavior of liver natural killer T cells (NKT cells) by intravital fluorescence microscopic imaging mice which a green fluorescent protein cDNA was used to replace gene encoding chemokine receptor CXCR6. NKT cells, account for most CXCR6+ liver, were found crawl within hepatic sinusoids at 10–20 μm/min and stop upon cell antigen activation. CXCR6-deficient exhibited selective severe reduction CD1d-reactive decreased susceptibility T-cell-dependent hepatitis. CXCL16,...

10.1371/journal.pbio.0030113 article EN cc-by PLoS Biology 2005-03-30
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