Department of Internal Medicine, Genome Research Center for Allergy and Respiratory Diseases, Soonchunhyang University Bucheon Hospital, Jung Dong, Wonmi Ku, Gyeonggi Do, Korea.
Hum Genet. 2010 Sep;128(3):293-302. doi: 10.1007/s00439-010-0850-3. Epub 2010 Jun 24.
Colony-stimulating factor 1 receptor (CSF1R) is expressed in monocytes/macrophages and dendritic cells. These cells play important roles in the innate immune response, which is regarded as an important aspect of asthma development. Genetic alterations in the CSF1R gene may contribute to the development of asthma. We investigated whether CSF1R gene polymorphisms were associated with the risk of asthma. Through direct DNA sequencing of the CSF1R gene, we identified 28 single nucleotide polymorphisms (SNPs) and genotyped them in 303 normal controls and 498 asthmatic patients. Expression of CSF1R protein and mRNA were measured on CD14-positive monocytes and neutrophils in peripheral blood of asthmatic patients using flow cytometry and real-time PCR. Among the 28 polymorphisms, two intronic polymorphism (+20511C>T and +22693T>C) were associated with the risk of asthma by logistic regression analysis. The frequencies of the minor allele at CSF1R +20511C>T and +22693T>C were higher in asthmatic subjects than in normal controls (4.6 vs. 7.7%, p = 0.001 in co-dominant and dominant models; 16.4 vs. 25.8%, p = 0.0006 in a recessive model). CSF1R mRNA levels in neutrophils of the asthmatic patients having the +22693CC allele were higher than in those having the +22693TT allele (p = 0.026). Asthmatic patients with the +22693CC allele also showed significantly higher CSF1R expression on CD14-positive monocytes and neutrophils than did those with the +22693TT allele (p = 0.045 and p = 0.044). The +20511C>T SNP had no association with CSF1R mRNA or protein expression. In conclusion, the minor allele at CSF1R +22693T>C may have a susceptibility effect in the development of asthma, via increased CSF1R protein and mRNA expression in inflammatory cells.
集落刺激因子 1 受体 (CSF1R) 在单核细胞/巨噬细胞和树突状细胞中表达。这些细胞在先天免疫反应中发挥重要作用,而先天免疫反应被认为是哮喘发展的一个重要方面。CSF1R 基因的遗传改变可能导致哮喘的发生。我们研究了 CSF1R 基因多态性是否与哮喘的发病风险相关。通过直接对 CSF1R 基因进行 DNA 测序,我们在 303 名正常对照者和 498 例哮喘患者中鉴定了 28 个单核苷酸多态性(SNP)并对其进行了基因分型。通过流式细胞术和实时 PCR 测量哮喘患者外周血中 CD14 阳性单核细胞和中性粒细胞中 CSF1R 蛋白和 mRNA 的表达。在这 28 个多态性中,通过逻辑回归分析,两个内含子多态性(+20511C>T 和 +22693T>C)与哮喘的发病风险相关。CSF1R +20511C>T 和 +22693T>C 位点的小等位基因在哮喘患者中的频率高于正常对照者(共显性和显性模型中分别为 4.6% vs. 7.7%,p=0.001;隐性模型中为 16.4% vs. 25.8%,p=0.0006)。携带 CSF1R +22693CC 等位基因的哮喘患者中性粒细胞中的 CSF1R mRNA 水平高于携带 CSF1R +22693TT 等位基因的患者(p=0.026)。携带 CSF1R +22693CC 等位基因的哮喘患者 CD14 阳性单核细胞和中性粒细胞中的 CSF1R 表达也显著高于携带 CSF1R +22693TT 等位基因的患者(p=0.045 和 p=0.044)。CSF1R +20511C>T SNP 与 CSF1R mRNA 或蛋白表达无关。总之,CSF1R +22693T>C 位点的小等位基因可能通过增加炎症细胞中的 CSF1R 蛋白和 mRNA 表达,在哮喘的发生发展中具有易感性。