scholarly journals Interleukin-7 receptor alpha is essential for the development of gamma delta + T cells, but not natural killer cells.

1996 ◽  
Vol 184 (1) ◽  
pp. 289-293 ◽  
Author(s):  
Y W He ◽  
T R Malek

Mice that lack a functional gamma c subunit of the receptors for interleukin (IL)-2, IL-4, IL-7, IL-9, and IL-15 display profound defects in lymphoid development. The IL-7/IL-7R system represents a critical interaction for conventional T and B cell development. In this report, the role of IL-7R alpha in the development of lymphoid lineages other than conventional T and B cells was examined. We demonstrate that gamma delta + T cells were absent in IL-7R alpha-deficient mice, whereas the development and function of natural killer cells were normal. Thus, IL-7R alpha function is required for the development of gamma delta + T cells but not natural killer cells.

Cytometry ◽  
1998 ◽  
Vol 32 (2) ◽  
pp. 109-119 ◽  
Author(s):  
Cynthia G. Healy ◽  
Jonathan W. Simons ◽  
Michael A. Carducci ◽  
Theodore L. Deweese ◽  
Michelle Bartkowski ◽  
...  

2006 ◽  
Vol 214 (1) ◽  
pp. 229-238 ◽  
Author(s):  
Francois Ghiringhelli ◽  
Cédric Ménard ◽  
Francois Martin ◽  
Laurence Zitvogel

Blood ◽  
2003 ◽  
Vol 101 (11) ◽  
pp. 4313-4321 ◽  
Author(s):  
Damien Reynaud ◽  
Nathalie Lefort ◽  
Elodie Manie ◽  
Laure Coulombel ◽  
Yves Levy

Abstract In this study we report the molecular and functional characterization of very early interleukin 7 receptor α (IL-7Rα)+-CD79a+CD19– B-cell progenitors, produced by human CD34+CD19–CD10– cord blood cells grown in the presence of stromal cells and cytokines. Purified IL-7Rα+CD79a+CD19– cells transcribed the B-lymphoid specific genes E2A, EBF, TdT, Rag-1, had initiated DJH rearrangements, but almost lacked Pax-5 mRNA. When exposed to appropriate environmental conditions, these cells repressed B-cell genes and completely differentiated into CD14+ macrophages, CD56+ natural killer cells, and CD4high T cells. Retention of the DJH rearranged genes in both CD14+ and CD56+ cells unambiguously demonstrates that early B-cell genes, expressed prior to Pax-5, can be activated in a multipotent human progenitor cell whose final fate, including in non-B lineages, is determined by external signals.


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