Identification of a Human Natural Killer Cell Lineage-Restricted Progenitor in Fetal and Adult Tissues

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Virginie M Renoux - , Lund University (Autor:in)
  • Alya Zriwil - , Lund University (Autor:in)
  • Claudia Peitzsch - , Lund Stem Cell Center, Lund University (Autor:in)
  • Jakob Michaëlsson - , Karolinska-Universitätskrankenhaus (Autor:in)
  • Danielle Friberg - , Karolinska-Universitätskrankenhaus (Autor:in)
  • Shamit Soneji - , Lund University (Autor:in)
  • Ewa Sitnicka - , Lund University (Autor:in)

Abstract

Natural killer (NK) cells are cytotoxic lymphocytes and play a vital role in controlling viral infections and cancer. In contrast to B and T lymphopoiesis where cellular and regulatory pathways have been extensively characterized, the cellular stages of early human NK cell commitment remain poorly understood. Here we demonstrate that a Lin(-)CD34(+)CD38(+)CD123(-)CD45RA(+)CD7(+)CD10(+)CD127(-) population represents a NK lineage-restricted progenitor (NKP) in fetal development, umbilical cord blood, and adult tissues. The newly identified NKP has robust NK cell potential both in vitro and in vivo, generates functionally cytotoxic NK cells, and lacks the ability to produce T cells, B cells, myeloid cells, and innate lymphoid-like cells (ILCs). Our findings identify an early step to human NK cell commitment and provide new insights into the human hematopoietic hierarchy.

Details

OriginalspracheEnglisch
Seiten (von - bis)394-407
Seitenumfang14
FachzeitschriftImmunity
Jahrgang43
Ausgabenummer2
PublikationsstatusVeröffentlicht - 18 Aug. 2015
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

Scopus 84940997861
ORCID /0000-0002-5247-908X/work/142241943

Schlagworte

Ziele für nachhaltige Entwicklung

Schlagwörter

  • Adult, Antigens, CD/metabolism, Cell Differentiation, Cell Lineage, Cytotoxicity, Immunologic, Fetal Blood/cytology, Fetal Development, Fetus/cytology, Hematopoiesis/immunology, Humans, Immunity, Innate, Immunophenotyping, Killer Cells, Natural/physiology, Lymphoid Progenitor Cells/physiology