首页> 美国卫生研究院文献>Frontiers in Endocrinology >Characterization of the Apelin/Elabela Receptors (APLNR) in Chickens Turtles and Zebrafish: Identification of a Novel Apelin-Specific Receptor in Teleosts
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Characterization of the Apelin/Elabela Receptors (APLNR) in Chickens Turtles and Zebrafish: Identification of a Novel Apelin-Specific Receptor in Teleosts

机译:鸡乌龟和斑马鱼中Apelin / Elabela受体(APLNR)的表征:硬骨鱼中新型Apelin特异性受体的鉴定

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摘要

Apelin receptor(s) (APLNR) are suggested to mediate the actions of apelin and Elabela (ELA) peptides in many physiological processes, including cardiovascular development and food intake in vertebrates. However, the functionality of APLNR has not been examined in most vertebrate groups. Here, we characterized two APLNRs APLNR1, APLNR2) in chickens and red-eared sliders, and three APLNRs in zebrafish (APLNR2a, APLNR2b, APLNR3a), which are homologous to human APLNR. Using luciferase-reporter assays or Western blot, we demonstrated that in chickens, APLNR1 (not APLNR2) expressed in HEK293 cells was potently activated by chicken apelin-36 and ELA-32 and coupled to Gi-cAMP and MAPK/ERK signaling pathways, indicating a crucial role of APLNR1 in mediating apelin/ELA actions; in red-eared sliders, APLNR2 (not APLNR1) was potently activated by apelin-36/ELA-32, suggesting that APLNR2 may mediate apelin/ELA actions; in zebrafish, both APLNR2a and APLNR2b were potently activated by apelin-36/ELA-32 and coupled to Gi-cAMP signaling pathway, as previously proposed, whereas the novel APLNR3a was specifically and potently activated by apelin. Similarly, an apelin-specific receptor (APLNR3b) sharing 57% sequence identity with zebrafish APLNR3a was identified in Nile tilapia. Collectively, our data facilitates the uncovering of the roles of APLNR signaling in different vertebrate groups and suggests a key functional switch between APLNR1 and APLNR2/3 in mediating the actions of ELA and apelin during vertebrate evolution.
机译:建议使用Apelin受体(APLNR)在许多生理过程中介导Apelin和Elabela(ELA)肽的作用,包括脊椎动物的心血管发育和食物摄取。但是,尚未在大多数脊椎动物中检查过APNNR的功能。在这里,我们表征了在鸡和红耳滑子中的两个APLNRs APLNR1,APNLR2)和在斑马鱼中的三个APLNRs(APNLR2a,APNLR2b,APNLR3a),它们与人APLNR同源。使用萤光素酶报告基因检测或Western印迹,我们证明了在鸡中,HEK293细胞中表达的APLNR1(非APLNR2)被鸡apelin-36和ELA-32有效激活,并与Gi-cAMP和MAPK / ERK信号通路偶联,表明APNNR1在介导apelin / ELA行为中起关键作用;在红耳滑子中,APLENR2(不是APLNR1)被apelin-36 / ELA-32有效激活,表明APLNR2可能介导apelin / ELA动作;在斑马鱼中,APLENR2a和APLNR2b均被apelin-36 / ELA-32强烈激活,并与Gi-cAMP信号通路偶联,如先前所提出的,而新型APLNR3a被apelin特异性激活。同样,在尼罗罗非鱼中鉴定出与斑马鱼APNLR3a具有57%序列同一性的apelin特异性受体(APNLR3b)。总的来说,我们的数据有助于揭示APLNR信号在不同脊椎动物群体中的作用,并暗示APNNR1和APLNR2 / 3之间在脊椎动物进化过程中介导ELA和apelin的作用之间的关键功能转换。

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