| 1. |
- Renoux, Virginie, et al.
(författare)
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Identification of a Human Natural Killer Cell Lineage-Restricted Progenitor in Fetal and Adult Tissues.
- 2015
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Ingår i: Immunity. - : Elsevier BV. - 1074-7613 .- 1097-4180. ; 43:2, s. 394-407
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Tidskriftsartikel (refereegranskat)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.
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| 2. |
- Tang, Yanjuan, et al.
(författare)
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Emergence of NK cell progenitors and functionally competent NK cell lineage subsets in the early mouse embryo.
- 2012
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Ingår i: Blood. - : American Society of Hematology. - 1528-0020 .- 0006-4971. ; 120:1, s. 63-75
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Tidskriftsartikel (refereegranskat)abstract
- The earliest stages of natural killer (NK) cell development are not well characterized. In this study, we investigated in different fetal hematopoietic tissues how NK cell progenitors and their mature NK cell progeny emerge and expand during fetal development. Here we demonstrate, for the first time, that the counterpart of adult bone marrow Lin(-)CD122(+)NK1.1(-)DX5(-) NK cell progenitor (NKP) emerges in the fetal liver at embryonic day (E) 13.5. Following NKP expansion, immature NK cells emerge at day E14.5 in the liver and E15.5 in the spleen. Thymic NK cells arise at day E15.5, while functionally competent cytotoxic NK cells were present in the liver and spleen at day E16.5 and E17.5, respectively. Fetal NKPs failed to produce B and myeloid cells, but sustained combined NK and T lineage potential at the single cell level. NKPs were also found in the fetal blood, spleen and thymus. These findings demonstrate the emergence and expansion of bipotent NK/T cell progenitor during fetal and adult lymphopoiesis, further supporting that NK/T lineage restriction is taking place prethymically. Uncovering the earliest NK cell developmental stages will provide important clues helping to understand the origin of diverse NK cell subsets, their progenitors and key regulators.
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