Institute of Biophysics, v.v.i., Academy of Sciences of the Czech Republic, Brno, Czech Republic.
Physiol Res. 2010;59(1):139-144. doi: 10.33549/physiolres.931724. Epub 2009 Feb 27.
Expression of mRNA for adenosine receptor subtypes A(1), A(2a), A(2b), and A(3) in normal and lipopolysaccharide (LPS)-activated murine RAW 264.7 macrophages has been investigated using the method of quantitative real-time polymerase chain reaction. The results have shown a very low, unquantifiable expression of adenosine A(1) receptor mRNA in both normal and LPS-activated macrophages. The other three adenosine receptor mRNAs have been found to be expressed at various but always quantifiable levels. Activation of the macrophages by LPS induced upregulation of the expression of adenosine receptor A(2a) and A(2b) mRNA, whereas the expression of adenosine receptor A(3) mRNA was downregulated. Unstimulated macrophages exhibited a high expression of the A(2b) adenosine receptor mRNA. The findings are discussed from the point of view of the antiinflammatory and hematopoiesis-stimulating roles of the adenosine receptor signaling.
使用定量实时聚合酶链反应方法,研究了腺苷受体亚型 A(1)、A(2a)、A(2b)和 A(3)在正常和脂多糖 (LPS) 激活的鼠 RAW 264.7 巨噬细胞中的 mRNA 表达。结果表明,在正常和 LPS 激活的巨噬细胞中,腺苷 A(1)受体 mRNA 的表达非常低,无法定量。其他三种腺苷受体 mRNA 的表达水平各不相同,但始终可以定量。LPS 激活巨噬细胞诱导腺苷受体 A(2a)和 A(2b)mRNA 的表达上调,而腺苷受体 A(3)mRNA 的表达下调。未受刺激的巨噬细胞表现出高表达的 A(2b)腺苷受体 mRNA。从腺苷受体信号的抗炎和造血刺激作用的角度讨论了这些发现。