Faculty of Medicine and Health Sciences, VIB-UGent Center for Medical Biotechnology, Flanders Institute for Biotechnology, Ghent University, A. Baertsoenkaai 3, 9000, Ghent, Belgium.
Inserm U1016, CNRS UMR 8104, Univ. Paris Descartes, Sorbonne Paris Cité, Institut Cochin, 22 rue Méchain, 75014, Paris, France.
Cell Mol Life Sci. 2019 Mar;76(6):1201-1214. doi: 10.1007/s00018-019-03004-9. Epub 2019 Jan 18.
Leptin links body energy stores to high energy demanding processes like reproduction and immunity. Based on leptin's role in autoimmune diseases and cancer, several leptin and leptin receptor (LR) antagonists have been developed, but these intrinsically lead to unwanted weight gain. Here, we report on the uncoupling of leptin's metabolic and immune functions based on the cross talk with the epidermal growth factor receptor (EGFR). We show that both receptors spontaneously interact and, remarkably, that this complex can partially overrule the lack of LR activation by a leptin antagonistic mutein. Moreover, this leptin mutant induces EGFR phosphorylation comparable to wild-type leptin. Exploiting this non-canonical leptin signalling pathway, we identified a camelid single-domain antibody that selectively inhibits this LR-EGFR cross talk without interfering with homotypic LR signalling. Administration in vivo showed that this single-domain antibody did not interfere with leptin's metabolic functions, but could reverse the leptin-driven protection against starvation-induced thymic and splenic atrophy. These findings offer new opportunities for the design and clinical application of selective leptin and LR antagonists that avoid unwanted metabolic side effects.
瘦素将身体的能量储存与生殖和免疫等高能量需求过程联系起来。基于瘦素在自身免疫性疾病和癌症中的作用,已经开发出几种瘦素和瘦素受体(LR)拮抗剂,但这些药物本质上会导致体重意外增加。在这里,我们根据与表皮生长因子受体(EGFR)的串扰,报告了瘦素代谢和免疫功能的解耦。我们表明,这两个受体自发相互作用,而且令人惊讶的是,这种复合物可以部分弥补瘦素拮抗突变体对 LR 激活的缺乏。此外,这种瘦素突变体诱导 EGFR 磷酸化,与野生型瘦素相当。利用这种非典型的瘦素信号通路,我们鉴定出一种骆驼科单域抗体,该抗体可选择性抑制 LR-EGFR 串扰,而不干扰同型 LR 信号。体内给药表明,该单域抗体不会干扰瘦素的代谢功能,但可以逆转瘦素对饥饿诱导的胸腺和脾脏萎缩的保护作用。这些发现为设计和临床应用选择性瘦素和 LR 拮抗剂提供了新的机会,这些拮抗剂可以避免不必要的代谢副作用。