LSSIG is a novel murine leukocyte-specific GPCR that is induced by the activation of STAT3

被引:78
作者
Senga, T
Iwamoto, S
Yoshida, T
Yokota, T
Adachi, K
Azuma, E
Hamaguchi, M
Iwamoto, T
机构
[1] Nagoya Univ, Sch Med, Radioisotope Res Ctr,Dept Mol Pathogenesis, Dept Ophthalmol,Div Med,Showa Ku, Aichi, Japan
[2] Mie Univ, Sch Med, Dept Pediat & Clin Immunol, Tsu, Mie 514, Japan
[3] Kanazawa Univ, Grad Sch Med Sci, Div Stem Cell Biol, Kanazawa, Ishikawa 920, Japan
关键词
D O I
10.1182/blood-2002-06-1881
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
G-protein-coupled receptors (GPCRs) transduce the signal of a wide variety of chemokines, cytokines, neurotransmitters, hormones, odorants, and others to regulate the biologic homeostasis, including hematopoiesis and immunity. Here we report the molecular cloning of leukocyte-specific STAT-induced GPCR (LSSIG), which is a novel murine orphan GPCR with the highest homology to human GPR43. The mRNA expression of LSSIG was clearly induced in M1 leukemia cells during the leukemia inhibitory factor (LIF)induced differentiation to macrophages, and the induction was evidently signal transducers and activators of transcription 3 (STAT3)-dependent. GPR43 expression was also strongly induced in HL-60 and U937 leukemia cells during the differentiation to monocytes. Further analysis showed that the expression of both LSSIG and GPR43 is highly restricted in hemato-poietic tissues. Cytokine-stimulation induced LSSIG and GPR43 in bone marrow cells, and monocytes and neutrophils, respectively. These results suggest that LSSIG and GPR43 might play pivotal roles in differentiation and immune response of monocytes and granulocytes. (C) 2003 by The American Society of Hematology.
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收藏
页码:1185 / 1187
页数:3
相关论文
共 17 条
[1]   TERMINAL DIFFERENTIATION OF HUMAN PROMYELOCYTIC LEUKEMIA-CELLS INDUCED BY DIMETHYL-SULFOXIDE AND OTHER POLAR COMPOUNDS [J].
COLLINS, SJ ;
RUSCETTI, FW ;
GALLAGHER, RE ;
GALLO, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (05) :2458-2462
[2]   Understanding GPCRs - from orphan receptors to novel drugs [J].
Dowell, SJ .
DRUG DISCOVERY TODAY, 2001, 6 (17) :884-+
[3]   Drug discovery: A historical perspective [J].
Drews, J .
SCIENCE, 2000, 287 (5460) :1960-1964
[4]   Roles of STAT3 in mediating the cell growth, differentiation and survival signals relayed through the IL-6 family of cytokine receptors [J].
Hirano, T ;
Ishihara, K ;
Hibi, M .
ONCOGENE, 2000, 19 (21) :2548-2556
[5]   IDENTIFYING DIFFERENCES IN MESSENGER-RNA EXPRESSION BY REPRESENTATIONAL DIFFERENCE ANALYSIS OF CDNA [J].
HUBANK, M ;
SCHATZ, DG .
NUCLEIC ACIDS RESEARCH, 1994, 22 (25) :5640-5648
[6]  
Kitamura T, 2000, METH MOL B, V134, P143
[7]   A pivotal role of Rho GTPase in the regulation of morphology and function of dendritic cells [J].
Kobayashi, M ;
Azuma, E ;
Ido, M ;
Hirayama, M ;
Jiang, Q ;
Iwamoto, S ;
Kumamoto, T ;
Yamamoto, H ;
Sakurai, M ;
Komada, Y .
JOURNAL OF IMMUNOLOGY, 2001, 167 (07) :3585-3591
[8]   CLONING THE DIFFERENCES BETWEEN 2 COMPLEX GENOMES [J].
LISITSYN, N ;
LISITSYN, N ;
WIGLER, M .
SCIENCE, 1993, 259 (5097) :946-951
[9]   Novel GPCRs and their endogenous ligands: expanding the boundaries of physiology and pharmacology [J].
Marchese, A ;
George, SR ;
Kolakowski, LF ;
Lynch, KR ;
O'Dowd, BF .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1999, 20 (09) :370-375
[10]   STAT3 activation is sufficient to maintain an undifferentiated state of mouse embryonic stem cells [J].
Matsuda, T ;
Nakamura, T ;
Nakao, K ;
Arai, T ;
Katsuki, M ;
Heike, T ;
Yokota, T .
EMBO JOURNAL, 1999, 18 (15) :4261-4269