Cloning and expression of feline colony stimulating factor receptor (CSF-1R) and analysis of the species specificity of stimulation by colony stimulating factor-1 (CSF-1) and interleukin-34 (IL-34)

被引:14
作者
Gow, Deborah J.
Garceau, Valerie
Pridans, Clare
Gow, Adam G.
Simpson, Kerry E.
Gunn-Moore, Danielle
Hume, David A. [1 ]
机构
[1] Univ Edinburgh, Roslin Inst, Easter Bush EH25 9RG, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
Macrophage; Ba/F3; Bone marrow; Species specificity; Renal; MESENCHYMAL STEM-CELLS; MARROW-DERIVED MACROPHAGES; BONE-MARROW; DENDRITIC CELLS; CYTOKINES IL-34; GENE-EXPRESSION; GM-CSF; FMS; DOXORUBICIN; TOXICITY;
D O I
10.1016/j.cyto.2012.11.014
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
Colony stimulating factor (CSF-1) and its receptor, CSF-1R, have been previously well studied in humans and rodents to dissect the role they play in development of cells of the mononuclear phagocyte system. A second ligand for the CSF-1R, IL-34 has been described in several species. In this study, we have cloned and expressed the feline CSF-1R and examined the responsiveness to CSF-1 and IL-34 from a range of species. The results indicate that pig and human CSF-1 and human IL-34 are equally effective in cats, where both mouse CSF-1 and IL-34 are significantly less active. Recombinant human CSF-1 can be used to generate populations of feline bone marrow and monocyte derived macrophages that can be used to further dissect macrophage-specific gene expression in this species, and to compare it to data derived from mouse, human and pig. These results set the scene for therapeutic use of CSF-1 and IL-34 in cats. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:630 / 638
页数:9
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