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斑马鱼胶质细胞源性神经营养因子(GDNF)及其共受体GFRα1激活人类RET受体,并在体外促进多巴胺能神经元的存活。

Zebrafish GDNF and its co-receptor GFRα1 activate the human RET receptor and promote the survival of dopaminergic neurons in vitro.

作者信息

Saarenpää Tuulia, Kogan Konstantin, Sidorova Yulia, Mahato Arun Kumar, Tascón Igor, Kaljunen Heidi, Yu Liying, Kallijärvi Jukka, Jurvansuu Jaana, Saarma Mart, Goldman Adrian

机构信息

Department of Biochemistry, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.

Institute of Biotechnology, University of Helsinki, Helsinki, Finland.

出版信息

PLoS One. 2017 May 3;12(5):e0176166. doi: 10.1371/journal.pone.0176166. eCollection 2017.

Abstract

Glial cell line-derived neurotrophic factor (GDNF) is a ligand that activates, through co-receptor GDNF family receptor alpha-1 (GFRα1) and receptor tyrosine kinase "RET", several signaling pathways crucial in the development and sustainment of multiple neuronal populations. We decided to study whether non-mammalian orthologs of these three proteins have conserved their function: can they activate the human counterparts? Using the baculovirus expression system, we expressed and purified Danio rerio RET, and its binding partners GFRα1 and GDNF, and Drosophila melanogaster RET and two isoforms of co-receptor GDNF receptor-like. Our results report high-level insect cell expression of post-translationally modified and dimerized zebrafish RET and its binding partners. We also found that zebrafish GFRα1 and GDNF are comparably active as mammalian cell-produced ones. We also report the first measurements of the affinity of the complex to RET in solution: at least for zebrafish, the Kd for GFRα1-GDNF binding RET is 5.9 μM. Surprisingly, we also found that zebrafish GDNF as well as zebrafish GFRα1 robustly activated human RET signaling and promoted the survival of cultured mouse dopaminergic neurons with comparable efficiency to mammalian GDNF, unlike E. coli-produced human proteins. These results contradict previous studies suggesting that mammalian GFRα1 and GDNF cannot bind and activate non-mammalian RET and vice versa.

摘要

胶质细胞系源性神经营养因子(GDNF)是一种配体,它通过共受体GDNF家族受体α-1(GFRα1)和受体酪氨酸激酶“RET”激活多个信号通路,这些信号通路对多种神经元群体的发育和维持至关重要。我们决定研究这三种蛋白质的非哺乳动物直系同源物是否保留了它们的功能:它们能否激活人类对应的蛋白?利用杆状病毒表达系统,我们表达并纯化了斑马鱼RET及其结合伴侣GFRα1和GDNF,以及果蝇RET和共受体GDNF受体样的两种异构体。我们的结果表明,经翻译后修饰和二聚化的斑马鱼RET及其结合伴侣在昆虫细胞中实现了高水平表达。我们还发现,斑马鱼GFRα1和GDNF与在哺乳动物细胞中产生的具有相当的活性。我们还首次测量了复合物在溶液中与RET的亲和力:至少对于斑马鱼来说,GFRα1-GDNF与RET结合的解离常数(Kd)为5.9 μM。令人惊讶的是,我们还发现,与大肠杆菌产生的人类蛋白不同,斑马鱼GDNF以及斑马鱼GFRα1能强有力地激活人类RET信号,并以与哺乳动物GDNF相当的效率促进培养的小鼠多巴胺能神经元的存活。这些结果与之前的研究相矛盾,之前的研究表明哺乳动物GFRα1和GDNF不能结合并激活非哺乳动物RET,反之亦然。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f1/5415192/e9dcad849424/pone.0176166.g001.jpg

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