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

Author:

Senga Takeshi1,Iwamoto Shotaro1,Yoshida Tsunehiko1,Yokota Takashi1,Adachi Koichi1,Azuma Eiichi1,Hamaguchi Michinari1,Iwamoto Takashi1

Affiliation:

1. From the Department of Molecular Pathogenesis, Department of Ophthalmology, Radioisotope Research Center Medical Division, Nagoya University School of Medicine, Showa-ku, Nagoya, Japan; Department of Pediatrics and Clinical Immunology, Mie University School of Medicine, Tsu, Japan; Division of Stem Cell Biology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.

Abstract

Abstract 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 hematopoietic 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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