Bazdar Douglas A, Kalinowska Magdalena, Panigrahi Soumya, Sieg Scott F
Division of Infectious Diseases and HIV Medicine, Case Western Reserve University School of Medicine, Cleveland, OH 44106; and.
Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461.
J Immunol. 2015 May 15;194(10):4698-704. doi: 10.4049/jimmunol.1400560. Epub 2015 Apr 13.
IL-7 is a key homeostatic cytokine that provides signals for T cell survival and proliferation in vivo. In this article, we provide evidence that IL-7 utilization is enhanced by a novel mechanism of cytokine "recycling" during which T cells treated with rIL-7 are rapidly induced to express p-STAT5 and are subsequently able to recycle biologically active cytokine for release to neighboring cells in soluble form. Our observations indicate that the ability of cells to recycle IL-7 is dependent on IL-7R α-chain (CD127) and endocytosis, consistent with a model whereby IL-7 is internalized via receptor interactions before recycling. These observations provide evidence of a novel mechanism that enables cells to optimally use IL-7.
白细胞介素-7(IL-7)是一种关键的稳态细胞因子,在体内为T细胞的存活和增殖提供信号。在本文中,我们提供证据表明,通过一种新型的细胞因子“循环利用”机制可增强IL-7的利用,在此过程中,用重组IL-7(rIL-7)处理的T细胞会迅速被诱导表达磷酸化信号转导和转录激活因子5(p-STAT5),随后能够将生物活性细胞因子循环利用,以可溶性形式释放到邻近细胞中。我们的观察结果表明,细胞循环利用IL-7的能力取决于IL-7受体α链(CD127)和内吞作用,这与IL-7在循环利用前通过受体相互作用被内化的模型一致。这些观察结果为细胞最佳利用IL-7的新机制提供了证据。