Weitz Hendrik T, Ettich Julia, Rafii Puyan, Wittich Christoph, Schultz Laura, Frank Nils C, Heise Denise, Krusche Matthias, Lokau Juliane, Garbers Christoph, Behnke Kristina, Floss Doreen M, Kolmar Harald, Moll Jens M, Scheller Jürgen
Institute of Biochemistry and Molecular Biology II, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Germany.
Institute of Clinical Biochemistry, Hannover Medical School, Germany.
FEBS J. 2025 Feb;292(3):523-536. doi: 10.1111/febs.17309. Epub 2024 Oct 29.
The cytokine interleukin 6 (IL-6) signals via the IL-6 α-receptor (IL-6Rα or IL-6R) in complex with the gp130 β-receptor. Cell type restricted expression of the IL-6R limits the action of IL-6 mainly to hepatocytes and some immune cells. Here, we show that IL-6 also binds to the IL-11 α receptor (IL-11Rα or IL-11R) and induces signaling via IL-11R:gp130 complexes, albeit with a lower affinity compared to IL-11. Antagonistic antibodies directed against IL-11R, but not IL-6R, inhibit IL-6 signaling via IL-11R:gp130 receptor complexes. Notably, IL-11 did not cross-react with IL-6R. IL-11R has also been identified as an alternative α receptor for the CNTF/IL-6-derived chimeric cytokine IC7, which has recently been shown to induce weight loss in mice. Accordingly, the effects of therapeutic monoclonal antibodies against IL-6 or IL-6R, which both block IL-6 signaling, may be slightly different. These findings provide new insights into IL-6 signaling and therefore offer new potential therapeutic intervention options in the future.
细胞因子白细胞介素6(IL-6)通过与gp130β受体形成复合物的IL-6α受体(IL-6Rα或IL-6R)进行信号传导。IL-6R的细胞类型限制性表达将IL-6的作用主要局限于肝细胞和一些免疫细胞。在此,我们表明IL-6也与IL-11α受体(IL-11Rα或IL-11R)结合,并通过IL-11R:gp130复合物诱导信号传导,尽管与IL-11相比亲和力较低。针对IL-11R而非IL-6R的拮抗抗体可抑制IL-6通过IL-11R:gp130受体复合物的信号传导。值得注意的是,IL-11与IL-6R没有交叉反应。IL-11R也已被确定为睫状神经营养因子/IL-6衍生的嵌合细胞因子IC7的替代α受体,最近已证明该细胞因子可诱导小鼠体重减轻。因此,两种均阻断IL-6信号传导的抗IL-6或抗IL-6R治疗性单克隆抗体的作用可能略有不同。这些发现为IL-6信号传导提供了新的见解,因此在未来提供了新的潜在治疗干预选择。