Next Article in Journal
Femtograms of Interferon-γ Suffice to Modulate the Behavior of Jurkat Cells: A New Light in Immunomodulation
Next Article in Special Issue
Type 1 Diabetes and Its Multi-Factorial Pathogenesis: The Putative Role of NK Cells
Previous Article in Journal
Physicochemical and Antimicrobial Characterization of Beeswax–Starch Food-Grade Nanoemulsions Incorporating Natural Antimicrobials
Previous Article in Special Issue
View Point: Semaphorin-3E: An Emerging Modulator of Natural Killer Cell Functions?
Article

Identification of Novel Human NK Cell Progenitor Subsets

1
The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, VIC 3052, Australia
2
Department of Medical Biology, University of Melbourne, Parkville, VIC 3050, Australia
3
Cord Blood Research, Murdoch Children’s Research Institute, Melbourne, VIC 3052, Australia
4
Department of Paediatrics, University of Melbourne, Melbourne, VIC 3010, Australia
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2017, 18(12), 2716; https://doi.org/10.3390/ijms18122716
Received: 31 October 2017 / Revised: 8 December 2017 / Accepted: 8 December 2017 / Published: 15 December 2017
(This article belongs to the Special Issue Natural Killer (NK) Cells)
Understanding the pathways and regulation of human haematopoiesis, in particular, lymphopoiesis, is vital to manipulation of these processes for therapeutic purposes. However, although haematopoiesis has been extensively characterised in mice, translation of these findings to human biology remains rudimentary. Here, we describe the isolation of three progenitor subsets from human foetal bone marrow that represent differential stages of commitment to the natural killer (NK) cell lineage based on IL-15 responsiveness. We identify CD7 as a marker of IL-15 responsive progenitors in human bone marrow and find that this expression is maintained throughout commitment and maturation. Within the CD7+ fraction, we focussed on the lineage potential of three subsets based on CD127 and CD117 expression and observed restricted lymphoid and biased NK cell potential amongst subsets. We further demonstrate the presence of subsets similar in both phenotype and function in umbilical cord blood and the bone marrow of humanised mice, validating these as appropriate sources of progenitors for the investigation of human haematopoiesis. Overall, we describe several stages in the process of lymphopoiesis that will form the basis of investigating the regulators of this process in humans. View Full-Text
Keywords: human haematopoiesis; lymphopoiesis; NK cell progenitors human haematopoiesis; lymphopoiesis; NK cell progenitors
Show Figures

Figure 1

MDPI and ACS Style

Sathe, P.; Pang, S.H.M.; Delconte, R.; Elwood, N.; Huntington, N.D. Identification of Novel Human NK Cell Progenitor Subsets. Int. J. Mol. Sci. 2017, 18, 2716. https://doi.org/10.3390/ijms18122716

AMA Style

Sathe P, Pang SHM, Delconte R, Elwood N, Huntington ND. Identification of Novel Human NK Cell Progenitor Subsets. International Journal of Molecular Sciences. 2017; 18(12):2716. https://doi.org/10.3390/ijms18122716

Chicago/Turabian Style

Sathe, Priyanka; Pang, Swee H.M.; Delconte, Rebecca; Elwood, Ngaire; Huntington, Nicholas D. 2017. "Identification of Novel Human NK Cell Progenitor Subsets" Int. J. Mol. Sci. 18, no. 12: 2716. https://doi.org/10.3390/ijms18122716

Find Other Styles
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Search more from Scilit
 
Search
Back to TopTop