Overproduction of PU.1 in mast cell progenitors: its effect on monocyte- and mast cell-specific gene expression

被引:22
作者
Nishiyama, C
Nishiyama, M
Ito, T
Masaki, S
Maeda, K
Masuoka, N
Yamane, H
Kitamura, T
Ogawa, H
Okumura, K
机构
[1] Juntendo Univ, Sch Med, Atopy Allergy Res Ctr, Bunkyo Ku, Tokyo 1138421, Japan
[2] Univ Tokyo, Inst Med Sci, Div Cellular Therapy, Minato Ku, Tokyo 1088639, Japan
[3] Univ Tokyo, Biotechnol Res Ctr, Bunkyo Ku, Tokyo 1138657, Japan
关键词
mast cells; monocyte; MHC class II; PU.1; transcription factor;
D O I
10.1016/j.bbrc.2003.11.145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Ets family transcription factor PU.1 is required for development of various lymphoid and myeloid cell lineages, and regulates the expression of several genes in a cell type-specific manner. Mouse bone marrow-derived hematopoietic progenitor cells are programmed to differentiate into mast cells, when the cells are maintained in the presence of pokeweed mitogen-stimulated spleen-conditioned medium. However, by retroviral introduction of PU.1 cDNA, the progenitor cells expressed MHC class II, CD11b, CD11c, and F4/80, and acquired the ability to stimulate T cells. Furthermore, PU.1-overproducing cells exhibited the morphology, in part, similar to that of monocyte. These results indicate that the mast cell progenitors still have the ability to express monocyte-specific genes by increased expression of PU.1. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:516 / 521
页数:6
相关论文
共 43 条
[1]   CD27, a member of the tumor necrosis factor receptor superfamily, activates NF-KB and stress-activated protein kinase/c-Jun N-terminal kinase via TRAF2, TRAF5, and NF-KB-inducing kinase [J].
Akiba, H ;
Nakano, H ;
Nishinaka, S ;
Shindo, M ;
Kobata, T ;
Atsuta, M ;
Morimoto, C ;
Ware, CF ;
Malinin, NL ;
Wallach, D ;
Yagita, H ;
Okumura, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :13353-13358
[2]   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
[3]   REPRESSION OF I-A-BETA GENE-EXPRESSION BY THE TRANSCRIPTION FACTOR PU.1 [J].
BORRAS, FE ;
LLOBERAS, J ;
MAKI, RA ;
CELADA, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (41) :24385-24391
[4]   CD34(+) hematopoietic progenitors from human cord blood differentiate along two independent dendritic cell pathways in response to GM-CSF+TNF alpha [J].
Caux, C ;
Vanbervliet, B ;
Massacrier, C ;
DezutterDambuyant, C ;
deSaintVis, B ;
Jacquet, C ;
Yoneda, K ;
Imamura, S ;
Schmitt, D ;
Banchereau, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :695-706
[5]   NEUTROPHILS AND MONOCYTES EXPRESS HIGH-LEVELS OF PU.1 (SPI-1) BUT NOT SPI-B [J].
CHEN, HM ;
ZHANG, P ;
VOSO, MT ;
HOHAUS, S ;
GONZALEZ, DA ;
GLASS, CK ;
ZHANG, DE ;
TENEN, DG .
BLOOD, 1995, 85 (10) :2918-2928
[6]   Regulation of macrophage and neutrophil cell fates by the PU.1:C/EBP ratio and granulocyte colony-stimulating factor [J].
Dahl, R ;
Walsh, JC ;
Lancki, D ;
Laslo, P ;
Iyer, SR ;
Singh, H ;
Simon, MC .
NATURE IMMUNOLOGY, 2003, 4 (10) :1029-1036
[7]   Regulation of B lymphocyte and macrophage development by graded expression of PU.1 [J].
DeKoter, RP ;
Singh, H .
SCIENCE, 2000, 288 (5470) :1439-1441
[8]   Polymorphisms in FcεRI β chain do not affect IgE-mediated mast cell activation [J].
Furumoto, Y ;
Hiraoka, S ;
Kawamoto, K ;
Masaki, S ;
Kitamura, T ;
Okumura, K ;
Ra, CS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (02) :765-771
[9]   MOUSE BETA-GLOBIN DNA-BINDING PROTEIN B1 IS IDENTICAL TO A PROTOONCOGENE, THE TRANSCRIPTION FACTOR SPI-1/PU.1, AND IS RESTRICTED IN EXPRESSION TO HEMATOPOIETIC-CELLS AND THE TESTIS [J].
GALSON, DL ;
HENSOLD, JO ;
BISHOP, TR ;
SCHALLING, M ;
DANDREA, AD ;
JONES, C ;
AURON, PE ;
HOUSMAN, DE .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (05) :2929-2941
[10]   PU.1 is required for myeloid-derived but not lymphoid-derived dendritic cells [J].
Guerriero, A ;
Langmuir, PB ;
Spain, LM ;
Scott, EW .
BLOOD, 2000, 95 (03) :879-885