Musso T, Varesio L, Zhang X, Rowe T K, Ferrara P, Ortaldo J R, O'Shea J J, McVicar D W
Biological Carcinogenesis and Development Program, Program Resources, Inc./DynCorp., National Cancer Institute-Frederick Cancer Research and Development Center, Maryland 21702-1201.
J Exp Med. 1994 Dec 1;180(6):2383-8. doi: 10.1084/jem.180.6.2383.
Lsk is a protein tyrosine kinase with homology to the COOH-terminal Src kinase (Csk). Unlike Csk that is ubiquitously expressed, Lsk has limited tissue distribution. Here we have examined the expression and regulation of Lsk and Csk in peripheral human monocytes. We have found that Lsk mRNA and protein were not expressed in resting monocytes but were induced by treatment with interleukin 4 (IL-4) or IL-13 but not by interferon gamma (IFN-gamma) or IL-2. In fact, IFN-gamma, but not IL-2, efficiently blocked Lsk induction by IL-4 or IL-13. In contrast, Csk was constitutively present in human monocytes and was upregulated by IFN-gamma but not by IL-4 or IL-13. These results suggest that despite their structural similarities, Lsk and Csk may play distinct regulatory roles in monocyte functions elicited by cytokines, with Lsk functioning specifically within the context of a Th2-type immune response.
Lsk是一种蛋白酪氨酸激酶,与COOH末端Src激酶(Csk)具有同源性。与广泛表达的Csk不同,Lsk的组织分布有限。在此,我们研究了Lsk和Csk在人外周血单核细胞中的表达及调控。我们发现,静止单核细胞中不表达Lsk mRNA和蛋白,但用白细胞介素4(IL-4)或IL-13处理可诱导其表达,而干扰素γ(IFN-γ)或IL-2则不能。事实上,IFN-γ而非IL-2能有效阻断IL-4或IL-13对Lsk的诱导。相反,Csk在人单核细胞中组成性存在,且被IFN-γ上调,但不被IL-4或IL-13上调。这些结果表明,尽管Lsk和Csk结构相似,但它们可能在细胞因子引发的单核细胞功能中发挥不同的调节作用,Lsk在Th2型免疫反应中具有特异性功能。