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Phenotypic diversity and plasticity in circulating neutrophil subpopulations in cancer

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-144102
  • Controversy surrounds neutrophil function in cancer because neutrophils were shown to provide both pro-and antitumor functions. We identified a heterogeneous subset of low-density neutrophils (LDNs) that appear transiently in self-resolving inflammation but accumulate continuously with cancer progression. LDNs display impaired neutrophil function and immunosuppressive properties, characteristics that are in stark contrast to those of mature, high-density neutrophils (HDNs). LDNs consist of both immature myeloid-derived suppressor cells (MDSCs)Controversy surrounds neutrophil function in cancer because neutrophils were shown to provide both pro-and antitumor functions. We identified a heterogeneous subset of low-density neutrophils (LDNs) that appear transiently in self-resolving inflammation but accumulate continuously with cancer progression. LDNs display impaired neutrophil function and immunosuppressive properties, characteristics that are in stark contrast to those of mature, high-density neutrophils (HDNs). LDNs consist of both immature myeloid-derived suppressor cells (MDSCs) and mature cells that are derived from HDNs in a TGF-beta-dependent mechanism. Our findings identify three distinct populations of circulating neutrophils and challenge the concept that mature neutrophils have limited plasticity. Furthermore, our findings provide a mechanistic explanation to mitigate the controversy surrounding neutrophil function in cancer.zeige mehrzeige weniger

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Autor(en): Jitka Y. Sagiv, Janna Michaeli, Simaan Assi, Inbal Mishalian, Hen Kisos, Liran Levy, Pazzit Damti, Delphine Lumbroso, Lola Polyansky, Ronit V. Sionov, Amiram Ariel, Avi-Hai Hovav, Erik Henke, Zvi G. Fridlender, Zvi Granot
URN:urn:nbn:de:bvb:20-opus-144102
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Institut für Anatomie und Zellbiologie
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Cell Reports
Erscheinungsjahr:2015
Band / Jahrgang:10
Heft / Ausgabe:4
Seitenangabe:562-573
Originalveröffentlichung / Quelle:Cell Reports 10:4, 562–573 (2015). DOI: 10.1016/j.celrep.2014.12.039
DOI:https://doi.org/10.1016/j.celrep.2014.12.039
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):TGF-beta; adenocarcinoma; inhibition; innate immunity; lung; mice; model; suppressor cells; tumor; tumorigenic properties
Datum der Freischaltung:14.06.2018
Lizenz (Deutsch):License LogoCC BY-NC-ND: Creative-Commons-Lizenz: Namensnennung, Nicht kommerziell, Keine Bearbeitung