Knorr Debbra Y, Rodriguez Polo Ignacio, Pies Hanna S, Schwedhelm-Domeyer Nicola, Pauls Stephanie, Behr Rüdiger, Heinrich Ralf
Department of Cellular Neurobiology, Johann-Friedrich-Blumenbach Institute for Zoology and Anthropology, Georg-August University Göttingen, Göttingen, Germany.
Department of Developmental Biology, Göttingen Center for Molecular Biosciences, Georg-August University Göttingen, Göttingen, Germany.
Front Mol Neurosci. 2023 Apr 6;16:1154509. doi: 10.3389/fnmol.2023.1154509. eCollection 2023.
The evolutionary conserved orphan cytokine receptor-like factor 3 (CRLF3) has been implicated in human disease, vertebrate hematopoiesis and insect neuroprotection. While its specific functions are elusive, experimental evidence points toward a general role in cell homeostasis. Erythropoietin (Epo) is a major regulator of vertebrate hematopoiesis and a general cytoprotective cytokine. Erythropoietic functions mediated by classical Epo receptor are understood in great detail whereas Epo-mediated cytoprotective mechanisms are more complex due to involvement of additional Epo receptors and a non-erythropoietic splice variant with selectivity for certain receptors. In the present study, we show that the human CRLF3 mediates neuroprotection upon activation with the natural Epo splice variant EV-3. We generated knock-out iPSC lines and differentiated them toward the neuronal lineage. While apoptotic death of rotenone-challenged wild type iPSC-derived neurons was prevented by EV-3, EV-3-mediated neuroprotection was absent in knock-out neurons. Rotenone-induced apoptosis and EV-3-mediated neuroprotection were associated with differential expression of pro-and anti-apoptotic genes. Our data characterize human CRLF3 as a receptor involved in Epo-mediated neuroprotection and identify CRLF3 as the first known receptor for EV-3.
进化保守的孤儿细胞因子受体样因子3(CRLF3)与人类疾病、脊椎动物造血作用和昆虫神经保护有关。虽然其具体功能尚不清楚,但实验证据表明它在细胞稳态中起一般作用。促红细胞生成素(Epo)是脊椎动物造血作用的主要调节因子,也是一种普遍的细胞保护细胞因子。经典Epo受体介导的红细胞生成功能已得到详细了解,而Epo介导的细胞保护机制则更为复杂,因为涉及额外的Epo受体和对某些受体具有选择性的非红细胞生成剪接变体。在本研究中,我们表明人类CRLF3在用天然Epo剪接变体EV-3激活后介导神经保护作用。我们生成了基因敲除的诱导多能干细胞系,并将它们分化为神经谱系。虽然鱼藤酮攻击的野生型诱导多能干细胞衍生神经元的凋亡死亡被EV-3阻止,但在基因敲除神经元中不存在EV-3介导的神经保护作用。鱼藤酮诱导的凋亡和EV-3介导的神经保护作用与促凋亡和抗凋亡基因的差异表达有关。我们的数据将人类CRLF3表征为参与Epo介导的神经保护作用的受体,并确定CRLF3是EV-3的首个已知受体。