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猫集落刺激因子受体(CSF-1R)的克隆与表达及集落刺激因子-1(CSF-1)和白细胞介素-34(IL-34)刺激的种属特异性分析。

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).

机构信息

The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Midlothian EH25 9RG Scotland, UK.

出版信息

Cytokine. 2013 Feb;61(2):630-8. doi: 10.1016/j.cyto.2012.11.014. Epub 2012 Dec 19.

DOI:10.1016/j.cyto.2012.11.014
PMID:23260168
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3573236/
Abstract

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.

摘要

集落刺激因子 (CSF-1) 及其受体 CSF-1R 在人类和啮齿动物中的研究已较为深入,以剖析其在单核吞噬细胞系统细胞发育中的作用。CSF-1R 的另一种配体 IL-34 在多种物种中已有描述。在这项研究中,我们克隆并表达了猫 CSF-1R,并检测了来自多种物种的 CSF-1 和 IL-34 的反应性。结果表明,猪和人 CSF-1 以及人 IL-34 在猫中同样有效,而鼠 CSF-1 和 IL-34 的活性明显较低。重组人 CSF-1 可用于生成猫骨髓和单核细胞衍生的巨噬细胞群体,可用于进一步剖析该物种中巨噬细胞特异性基因表达,并与来自小鼠、人类和猪的数据进行比较。这些结果为 CSF-1 和 IL-34 在猫中的治疗用途奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/4f6adfb3fec6/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/4ba69352d93f/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/b00d20070168/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/aa426fe15abc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/b31886e4bf81/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/3e6e970a583d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/96e93cc3287e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/4e3472c15f95/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/4f6adfb3fec6/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/4ba69352d93f/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/b00d20070168/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/aa426fe15abc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/b31886e4bf81/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/3e6e970a583d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/96e93cc3287e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/4e3472c15f95/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b378/3573236/4f6adfb3fec6/gr8.jpg

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