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首页> 外文期刊>Frontiers in zoology >Eel osmotic stress transcriptional factor 1 (Ostf1) is highly expressed in gill mitochondria-rich cells, where ERK phosphorylated
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Eel osmotic stress transcriptional factor 1 (Ostf1) is highly expressed in gill mitochondria-rich cells, where ERK phosphorylated

机译:鳗鱼渗透应激转录因子1(Ostf1)在富含g线粒体的细胞中高度表达,其中ERK磷酸化

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Background Osmotic stress transcriptional factor 1 (Ostf1) was firstly identified in tilapia in 2005. Then numerous studies have investigated its regulation and expression profile in fish gill tissues in related to osmoregulation. Generally, hyperosmotic stress induced ostf1 mRNA expression level, however there is no report studying the cellular localization of Ostf1 expression in any osmoregulatory tissue. In this study immunohistochemical (IHC) approach was used to study the cellular localization of Ostf1 in gill cells of Japanese eels. Findings Ostf1 protein was found to be localized in branchial mitochondria-rich/chloride cell (MRC/CC) as revealed by Naα5 and CFTR co-localization. The protein was detectable at day 3 after fresh water to seawater transfer and was mainly localized in MRCs. Moreover, elevated levels of extracellular signal regulated kinase (ERK) phosphorylation was observed at day 3 of the transfer and was co-localized with MRCs. Conclusions Our data identified Ostf1 expression in gill MRCs. The observation supports the role of Ostf1 in osmosensing and/or osmoregulation in fish gills, particularly its functional relationship with MRCs. The observation of the co-expression of pERK and Ostf1 in MRCs suggests a cross-talk mechanism between the mitogen-activated protein kinases (MAPKs) and Ostf1 in response to hyperosmotic challenge. To summarize, this report has addressed the cellular localization of Ostf1 and provides evidence to illustrate the involvement of Ostf1 and ERK on osmosensing and osmoregulatory function of gill MRCs.
机译:背景技术渗透胁迫转录因子1(Ostf1)于2005年在罗非鱼中首次发现。然后,许多研究调查了其在鱼g组织中与渗透压调节有关的调控和表达谱。通常,高渗胁迫诱导ostf1 mRNA表达水平,但是,没有研究研究任何渗透调节组织中Ostf1表达的细胞定位。在这项研究中,采用免疫组织化学(IHC)方法研究了日本鳗g细胞中Ostf1的细胞定位。结果发现Naf5和CFTR共定位显示,Ostf1蛋白位于富含分支线粒体/氯化物的细胞(MRC / CC)中。在淡水到海水转移后的第3天可检测到该蛋白,并且主要定位在MRC中。此外,在转移的第3天观察到细胞外信号调节激酶(ERK)磷酸化水平升高,并且与MRCs共定位。结论我们的数据确定了Ost MRC中的Ostf1表达。该观察结果支持Ostf1在鱼fish的渗透和/或渗透调节中的作用,特别是其与MRC的功能关系。对pERK和Ostf1在MRCs中共表达的观察表明,响应高渗挑战,有丝分裂原激活的蛋白激酶(MAPK)和Ostf1之间存在串扰机制。总而言之,该报告解决了Ostf1的细胞定位问题,并提供了证据来说明Ostf1和ERK与g MRC的渗透压和渗透调节功能有关。

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