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A molecular map of murine lymph node blood vascular endothelium at single cell resolution.
Brulois, Kevin; Rajaraman, Anusha; Szade, Agata; Nordling, Sofia; Bogoslowski, Ania; Dermadi, Denis; Rahman, Milladur; Kiefel, Helena; O'Hara, Edward; Koning, Jasper J; Kawashima, Hiroto; Zhou, Bin; Vestweber, Dietmar; Red-Horse, Kristy; Mebius, Reina E; Adams, Ralf H; Kubes, Paul; Pan, Junliang; Butcher, Eugene C.
  • Brulois K; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Rajaraman A; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Szade A; Palo Alto Veterans Institute for Research, Palo Alto, CA, USA.
  • Nordling S; Department of Molecular Cell Biology and Immunology, Vrije Universiteit Medical Center, Amsterdam, The Netherlands.
  • Bogoslowski A; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Dermadi D; Department of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.
  • Rahman M; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Kiefel H; Calvin, Phoebe & Joan Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada.
  • O'Hara E; Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada.
  • Koning JJ; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Kawashima H; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Zhou B; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Vestweber D; Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Red-Horse K; Department of Molecular Cell Biology and Immunology, Vrije Universiteit Medical Center, Amsterdam, The Netherlands.
  • Mebius RE; Department of Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan.
  • Adams RH; The State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, 200031, Beijing, China.
  • Kubes P; Department Vascular Cell Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
  • Pan J; Department of Biology, Stanford University, Stanford, CA, USA.
  • Butcher EC; Department of Molecular Cell Biology and Immunology, Vrije Universiteit Medical Center, Amsterdam, The Netherlands.
Nat Commun ; 11(1): 3798, 2020 07 30.
Article en En | MEDLINE | ID: mdl-32732867
Blood vascular endothelial cells (BECs) control the immune response by regulating blood flow and immune cell recruitment in lymphoid tissues. However, the diversity of BEC and their origins during immune angiogenesis remain unclear. Here we profile transcriptomes of BEC from peripheral lymph nodes and map phenotypes to the vasculature. We identify multiple subsets, including a medullary venous population whose gene signature predicts a selective role in myeloid cell (vs lymphocyte) recruitment to the medulla, confirmed by videomicroscopy. We define five capillary subsets, including a capillary resident precursor (CRP) that displays stem cell and migratory gene signatures, and contributes to homeostatic BEC turnover and to neogenesis of high endothelium after immunization. Cell alignments show retention of developmental programs along trajectories from CRP to mature venous and arterial populations. Our single cell atlas provides a molecular roadmap of the lymph node blood vasculature and defines subset specialization for leukocyte recruitment and vascular homeostasis.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Endotelio Vascular / Linfocitos / Células Mieloides / Células Endoteliales / Ganglios Linfáticos Límite: Animals Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Endotelio Vascular / Linfocitos / Células Mieloides / Células Endoteliales / Ganglios Linfáticos Límite: Animals Idioma: En Año: 2020 Tipo del documento: Article