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Tumor-Promoting Ly-6G+ SiglecFhigh Cells Are Mature and Long-Lived Neutrophils.
Pfirschke, Christina; Engblom, Camilla; Gungabeesoon, Jeremy; Lin, Yunkang; Rickelt, Steffen; Zilionis, Rapolas; Messemaker, Marius; Siwicki, Marie; Gerhard, Genevieve M; Kohl, Anna; Meylan, Etienne; Weissleder, Ralph; Klein, Allon M; Pittet, Mikael J.
Afiliação
  • Pfirschke C; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Engblom C; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Gungabeesoon J; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Lin Y; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Rickelt S; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Zilionis R; Institute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Messemaker M; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Siwicki M; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Gerhard GM; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Kohl A; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
  • Meylan E; Swiss Institute for Experimental Cancer Research, School of Life Sciences, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
  • Weissleder R; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA; Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.
  • Klein AM; Department of Systems Biology, Harvard Medical School, Boston, MA, USA.
  • Pittet MJ; Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA; Department of Pathology and Immunology, University of Geneva, Geneva, Switzerland; Department of Oncology, Geneva University Hospitals, Geneva, Switzerland. Electronic address:
Cell Rep ; 32(12): 108164, 2020 09 22.
Article em En | MEDLINE | ID: mdl-32966785
ABSTRACT
Myeloid cells co-expressing the markers CD11b, Ly-6G, and SiglecF can be found in large numbers in murine lung adenocarcinomas and accelerate cancer growth by fostering tumor cell invasion, angiogenesis, and immunosuppression; however, some of these cells' fundamental features remain unexplored. Here, we show that tumor-infiltrating CD11b+ Ly-6G+ SiglecFhigh cells are bona fide mature neutrophils and therefore differ from other myeloid cells, including SiglecFhigh eosinophils, SiglecFhigh macrophages, and CD11b+ Ly-6G+ myeloid-derived suppressor cells. We further show that SiglecFhigh neutrophils gradually accumulate in growing tumors, where they can live for several days; this lifespan is in marked contrast to that of their SiglecFlow counterparts and neutrophils in general, which live for several hours only. Together, these findings reveal distinct attributes for tumor-promoting SiglecFhigh neutrophils and help explain their deleterious accumulation in the tumor bed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos Ly / Lectinas Semelhantes a Imunoglobulina de Ligação ao Ácido Siálico / Adenocarcinoma de Pulmão / Neoplasias Pulmonares / Neutrófilos Limite: Animals Idioma: En Revista: Cell Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos Ly / Lectinas Semelhantes a Imunoglobulina de Ligação ao Ácido Siálico / Adenocarcinoma de Pulmão / Neoplasias Pulmonares / Neutrófilos Limite: Animals Idioma: En Revista: Cell Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos