Differential requirement for the transcription factor PU.1 in the generation of natural killer cells versus B and T cells

被引:111
作者
Colucci, F
Samson, SI
DeKoter, RP
Lantz, O
Singh, H
Di Santo, JP
机构
[1] Inst Pasteur, Dept Immunol, Lab Cytokines & Lymphoid Dev, F-75015 Paris, France
[2] Univ Chicago, Howard Hughes Med Inst, Chicago, IL 60637 USA
[3] Hop Necker Enfants Malad, INSERM, U25, Paris, France
关键词
D O I
10.1182/blood.V97.9.2625
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PU.1 is a member of the Ets family of transcription factors required for the development of various lymphoid and myeloid cell lineages, but its role in natural killer (NK) cell development is not known. The study shows that PU.1 is expressed in NK cells and that, on cell transfer into alymphoid Rag2/gammac(-/-) mice, hematopoietic progenitors of PU.1(-/-) fetal liver cells could generate functional NK cells but not B or T cells. Nevertheless, the numbers of bone marrow NK cell precursors and splenic mature NK cells were reduced compared to controls. Moreover, PU.1(-/-) NK cells displayed reduced expression of the receptors for stem cell factor and interleukin (IL)-7, suggesting a nonredundant role for PU.1 in regulating the expression of these cytokine receptor genes during NK cell development. PU.1(-/-) NK cells also showed defective expression of inhibitory and activating members of the Ly49 family and failed to proliferate in response to IL-2 and IL-12. Thus, despite the less stringent requirement for PU.1 in NK cell development compared to B and T cells, PU.1 regulates NK cell differentiation and homeostasis. (Blood, 2001;97:2625-2632) (C) 2001 by The American Society of Hematology.
引用
收藏
页码:2625 / 2632
页数:8
相关论文
共 49 条
[1]   A clonogenic common myeloid progenitor that gives rise to all myeloid lineages [J].
Akashi, K ;
Traver, D ;
Miyamoto, T ;
Weissman, IL .
NATURE, 2000, 404 (6774) :193-197
[2]   Neutrophils deficient in PU.1 do not terminally differentiate or become functionally competent [J].
Anderson, KL ;
Smith, KA ;
Pio, F ;
Torbett, BE ;
Maki, RA .
BLOOD, 1998, 92 (05) :1576-1585
[3]   Transcription factor PU.1 is necessary for development of thymic and myeloid progenitor-derived dendritic cells [J].
Anderson, KL ;
Perkin, H ;
Surh, CD ;
Venturini, S ;
Maki, RA ;
Torbett, BE .
JOURNAL OF IMMUNOLOGY, 2000, 164 (04) :1855-1861
[4]  
Anderson MK, 1999, DEVELOPMENT, V126, P3131
[5]   The Ets-1 transcription factor is required for the development of natural killer cells in mice [J].
Barton, K ;
Muthusamy, N ;
Fischer, C ;
Ting, CN ;
Walunas, TL ;
Lanier, LL ;
Leiden, JM .
IMMUNITY, 1998, 9 (04) :555-563
[6]  
Bassuk AG, 1997, ADV IMMUNOL, V64, P65, DOI 10.1016/S0065-2776(08)60887-1
[7]   INCREASED T-CELL APOPTOSIS AND TERMINAL B-CELL DIFFERENTIATION-INDUCED BY INACTIVATION OF THE ETS-1 PROTOONCOGENE [J].
BORIES, JC ;
WILLERFORD, DM ;
GREVIN, D ;
DAVIDSON, L ;
CAMUS, A ;
MARTIN, P ;
STEHELIN, D ;
ALT, FW .
NATURE, 1995, 377 (6550) :635-638
[8]   The natural killer gene complex: A genetic basis for understanding natural killer cell function and innate immunity [J].
Brown, MG ;
Scalzo, AA ;
Matsumoto, K ;
Yokoyama, WM .
IMMUNOLOGICAL REVIEWS, 1997, 155 :53-65
[9]   Identification of a novel developmental stage marking lineage commitment of progenitor thymocytes [J].
Carlyle, JR ;
Michie, AM ;
Furlonger, C ;
Nakano, T ;
Lenardo, MJ ;
Paige, CJ ;
ZunigaPflucker, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (02) :173-182
[10]   The receptor tyrosine kinase c-kit provides a critical signal for survival, expansion, and maturation of mouse natural killer cells [J].
Colucci, F ;
Di Santo, JP .
BLOOD, 2000, 95 (03) :984-991