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Endothelial junctional membrane protrusions serve as hotspots for neutrophil transmigration.
Arts, Janine Jg; Mahlandt, Eike K; Grönloh, Max Lb; Schimmel, Lilian; Noordstra, Ivar; Gordon, Emma; van Steen, Abraham Ci; Tol, Simon; Walzog, Barbara; van Rijssel, Jos; Nolte, Martijn A; Postma, Marten; Khuon, Satya; Heddleston, John M; Wait, Eric; Chew, Teng Leong; Winter, Mark; Montanez, Eloi; Goedhart, Joachim; van Buul, Jaap D.
Afiliação
  • Arts JJ; Molecular Cell Biology Lab at Dept. Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
  • Mahlandt EK; Leeuwenhoek Centre for Advanced Microscopy (LCAM), section Molecular Cytology at Swammerdam Institute for Life Sciences (SILS) at University of Amsterdam, Amsterdam, Netherlands.
  • Grönloh ML; Leeuwenhoek Centre for Advanced Microscopy (LCAM), section Molecular Cytology at Swammerdam Institute for Life Sciences (SILS) at University of Amsterdam, Amsterdam, Netherlands.
  • Schimmel L; Molecular Cell Biology Lab at Dept. Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
  • Noordstra I; Leeuwenhoek Centre for Advanced Microscopy (LCAM), section Molecular Cytology at Swammerdam Institute for Life Sciences (SILS) at University of Amsterdam, Amsterdam, Netherlands.
  • Gordon E; Molecular Cell Biology Lab at Dept. Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
  • van Steen AC; Leeuwenhoek Centre for Advanced Microscopy (LCAM), section Molecular Cytology at Swammerdam Institute for Life Sciences (SILS) at University of Amsterdam, Amsterdam, Netherlands.
  • Tol S; Division of Cell and Developmental Biology, Institute for Molecular Bioscience, The University of Queensland, BrisbaneQLD, Australia.
  • Walzog B; Division of Cell and Developmental Biology, Institute for Molecular Bioscience, The University of Queensland, BrisbaneQLD, Australia.
  • van Rijssel J; Division of Cell and Developmental Biology, Institute for Molecular Bioscience, The University of Queensland, BrisbaneQLD, Australia.
  • Nolte MA; Molecular Cell Biology Lab at Dept. Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
  • Postma M; Molecular Cell Biology Lab at Dept. Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
  • Khuon S; Department of Cardiovascular Physiology and Pathophysiology, Walter Brendel Center of Experimental Medicine, Biomedical Center, Ludwig-Maximilians-Universität München, Planegg-Martinsried, Germany.
  • Heddleston JM; Molecular Cell Biology Lab at Dept. Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
  • Wait E; Molecular Cell Biology Lab at Dept. Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
  • Chew TL; Leeuwenhoek Centre for Advanced Microscopy (LCAM), section Molecular Cytology at Swammerdam Institute for Life Sciences (SILS) at University of Amsterdam, Amsterdam, Netherlands.
  • Winter M; Advanced Imaging Center at Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
  • Montanez E; Advanced Imaging Center at Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
  • Goedhart J; Microscopy Facility at the Cleveland Clinic Florida Research and Innovation Center, Port St. Lucie, United States.
  • van Buul JD; Advanced Imaging Center at Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
Elife ; 102021 08 25.
Article em En | MEDLINE | ID: mdl-34431475
ABSTRACT
Upon inflammation, leukocytes rapidly transmigrate across the endothelium to enter the inflamed tissue. Evidence accumulates that leukocytes use preferred exit sites, alhough it is not yet clear how these hotspots in the endothelium are defined and how they are recognized by the leukocyte. Using lattice light sheet microscopy, we discovered that leukocytes prefer endothelial membrane protrusions at cell junctions for transmigration. Phenotypically, these junctional membrane protrusions are present in an asymmetric manner, meaning that one endothelial cell shows the protrusion and the adjacent one does not. Consequently, leukocytes cross the junction by migrating underneath the protruding endothelial cell. These protrusions depend on Rac1 activity and by using a photo-activatable Rac1 probe, we could artificially generate local exit-sites for leukocytes. Overall, we have discovered a new mechanism that uses local induced junctional membrane protrusions to facilitate/steer the leukocyte escape/exit from inflamed vessel walls.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Junções Intercelulares / Neutrófilos Limite: Animals / Humans / Male Idioma: En Revista: Elife Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Junções Intercelulares / Neutrófilos Limite: Animals / Humans / Male Idioma: En Revista: Elife Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda