Shenzhen Key Laboratory of Marine Bioresource & Eco-Environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518060, China.
BMC Genomics. 2022 Jul 30;23(1):545. doi: 10.1186/s12864-022-08784-2.
Scatophagus argus, an estuarine inhabitant, can rapidly adapt to different salinity environments. However, the knowledge of the molecular mechanisms underlying its strong salinity tolerance remains unclear. The gill, as the main osmoregulatory organ, plays a vital role in the salinity adaptation of the fish, and thus relative studies are constructive to reveal unique osmoregulatory mechanisms in S. argus.
In the present study, iTRAQ coupled with nanoLC-MS/MS techniques were employed to explore branchial osmoregulatory mechanisms in S. argus acclimated to different salinities. Among 1,604 identified proteins, 796 differentially expressed proteins (DEPs) were detected. To further assess osmoregulatory strategies in the gills under different salinities, DEPs related to osmoregulatory (22), non-directional (18), hypo- (52), and hypersaline (40) stress responses were selected. Functional annotation analysis of these selected DEPs indicated that the cellular ion regulation (e.g. Na-K-ATPase [NKA] and Na-K-2Cl cotransporter 1 [NKCC1]) and ATP synthesis were deeply involved in the osmoregulatory process. As an osmoregulatory protein, NKCC1 expression was inhibited under hyposaline stress but showed the opposite trend in hypersaline conditions. The expression levels of NKA α1 and β1 were only increased under hypersaline challenge. However, hyposaline treatments could enhance branchial NKA activity, which was inhibited under hypersaline environments, and correspondingly, reduced ATP content was observed in gill tissues exposed to hyposaline conditions, while its contents were increased in hypersaline groups. In vitro experiments indicated that Na, K, and Cl ions were pumped out of branchial cells under hypoosmotic stress, whereas they were absorbed into cells under hyperosmotic conditions. Based on our results, we speculated that NKCC1-mediated Na influx was inhibited, and proper Na efflux was maintained by improving NKA activity under hyposaline stress, promoting the rapid adaptation of branchial cells to the hyposaline condition. Meanwhile, branchial cells prevented excessive loss of ions by increasing NKA internalization and reducing ATP synthesis. In contrast, excess ions in cells exposed to the hyperosmotic medium were excreted with sufficient energy supply, and reduced NKA activity and enhanced NKCC1-mediated Na influx were considered a compensatory regulation.
S. argus exhibited divergent osmoregulatory strategies in the gills when encountering hypoosmotic and hyperosmotic stresses, facilitating effective adaptabilities to a wide range of environmental salinity fluctuation.
沙塘鳢是一种栖息于河口的鱼类,能够快速适应不同盐度的环境。然而,其强耐盐性的分子机制尚不清楚。鳃作为主要的渗透压调节器官,在鱼类的盐度适应中起着至关重要的作用,因此相关研究有助于揭示沙塘鳢独特的渗透压调节机制。
本研究采用 iTRAQ 联合纳升 LC-MS/MS 技术,探讨了不同盐度下沙塘鳢鳃部渗透压调节机制。在鉴定的 1604 种蛋白质中,检测到 796 种差异表达蛋白(DEPs)。为了进一步评估不同盐度下鳃部的渗透压调节策略,选择了与渗透压调节(22 个)、非定向(18 个)、低盐(52 个)和高盐(40 个)应激反应相关的 DEPs。对这些选定的 DEPs 的功能注释分析表明,细胞离子调节(如 Na-K-ATP 酶[NKA]和 Na-K-2Cl 协同转运蛋白 1 [NKCC1])和 ATP 合成在渗透压调节过程中深度参与。作为一种渗透压调节蛋白,NKCC1 在低盐胁迫下的表达受到抑制,但在高盐条件下则呈现相反的趋势。NKAα1 和β1 的表达水平仅在高盐胁迫下增加。然而,低盐处理可以增强鳃部 NKA 的活性,而在高盐环境中则受到抑制,相应地,低盐组鳃组织中的 ATP 含量降低,而高盐组中的含量增加。体外实验表明,在低渗胁迫下,Na+、K+和 Cl-离子从鳃细胞中泵出,而在高渗条件下则被吸收到细胞内。根据我们的结果,我们推测在低盐胁迫下,通过提高 NKA 的活性抑制 NKCC1 介导的 Na+内流,并维持适当的 Na+外流,促进鳃细胞快速适应低盐环境。同时,通过增加 NKA 的内化和减少 ATP 合成,鳃细胞防止离子过度流失。相反,在高渗培养基中暴露的细胞中过量的离子通过充足的能量供应排出,并且降低 NKA 活性和增强 NKCC1 介导的 Na+内流被认为是一种代偿性调节。
沙塘鳢在应对低渗和高渗胁迫时,在鳃部表现出不同的渗透压调节策略,有助于有效适应广泛的环境盐度波动。