Department of Biology and Laurier Institute for Water Science, Wilfrid Laurier University, Waterloo, ON, N2L 3C5, Canada.
J Comp Physiol B. 2020 Nov;190(6):701-715. doi: 10.1007/s00360-020-01305-1. Epub 2020 Aug 27.
Sea lamprey (Petromyzon marinus) begin life as filter-feeding larvae (ammocoetes) before undergoing a complex metamorphosis into parasitic juveniles, which migrate to the sea where they feed on the blood of large-bodied fishes. The greater protein intake during this phase results in marked increases in the production of nitrogenous wastes (N-waste), which are excreted primarily via the gills. However, it is unknown how gill structure and function change during metamorphosis and how it is related to modes of ammonia excretion, nor do we have a good understanding of how the sea lamprey's transition from fresh water (FW) to sea water (SW) affects patterns and mechanisms of N-waste excretion in relation to ionoregulation. Using immunohistochemistry, we related changes in the gill structure of larval, metamorphosing, and juvenile sea lampreys to their patterns of ammonia excretion (J) and urea excretion (J) in FW, and following FW to artificial seawater (ASW) transfer. Rates of J and J were low in larval sea lamprey and increased in feeding juvenile, parasitic sea lamprey. In freshwater-dwelling ammocoetes, immunohistochemical analysis revealed that Rhesus glycoprotein C-like protein (Rhcg-like) was diffusely distributed on the lamellar epithelium, but following metamorphosis, Rhcg-like protein was restricted to SW mitochondrion-rich cells (MRCs; ionocytes) between the gill lamellae. Notably, these interlamellar Rhcg-like proteins co-localized with Na/K-ATPase (NKA), which increased in expression and activity by almost tenfold during metamorphosis. The distribution of V-type H-ATPase (V-ATPase) on the lamellae decreased following metamorphosis, indicating it may have a more important role in acid-base regulation and Na uptake in FW, compared to SW. We conclude that the re-organization of the sea lamprey gill during metamorphosis not only plays a critical role in allowing them to cope with greater salinity following the FW-SW transition, but that it simultaneously reflects fundamental changes in methods used to excrete ammonia.
海七鳃鳗(Petromyzon marinus)在经历复杂的变态过程成为寄生幼体之前,是以滤食方式生活的幼虫(幼鳗),这些幼体迁移到海里以吸食大型鱼类的血液为生。在此阶段,由于摄入更多的蛋白质,氮废物(N 废物)的产生显著增加,这些废物主要通过鳃排出。然而,我们尚不清楚在变态过程中鳃的结构和功能如何变化,以及它与氨排泄方式有何关系,也不了解海七鳃鳗从淡水(FW)过渡到海水(SW)如何影响与离子调节相关的 N 废物排泄的模式和机制。我们利用免疫组织化学方法,将幼虫、变态期和幼体海七鳃鳗的鳃结构变化与它们在 FW 中的氨排泄(J)和尿素排泄(J)模式相关联,并在 FW 到人工海水(ASW)转移后进行研究。在幼虫海七鳃鳗中,J 和 J 的速率较低,而在摄食幼体、寄生海七鳃鳗中则增加。在淡水栖息的幼鳗中,免疫组织化学分析显示,恒河猴糖蛋白 C 样蛋白(Rhcg-like)广泛分布在鳃片上皮,但在变态后,Rhcg-like 蛋白仅限于鳃片之间的 SW 富线粒体细胞(MRCs;离子细胞)。值得注意的是,这些跨鳃片 Rhcg-like 蛋白与 Na/K-ATPase(NKA)共定位,NKA 的表达和活性在变态过程中增加了近十倍。V-型 H+-ATPase(V-ATPase)在鳃片上的分布在变态后减少,这表明它在 FW 中的酸碱调节和 Na 摄取中可能比 SW 更重要。我们得出结论,海七鳃鳗在变态过程中鳃的重新组织不仅对它们在从 FW 到 SW 过渡后应对更高盐度起着至关重要的作用,而且同时反映了它们排泄氨的方法发生了根本变化。