Departamento de Biologia, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.
Centro de Biologia Marinha, Universidade de São Paulo, São Sebastião, SP, Brazil.
J Exp Zool A Ecol Integr Physiol. 2017 Jul;327(6):380-397. doi: 10.1002/jez.2109. Epub 2017 Sep 12.
Fresh caught Clibanarius vittatus [SW, 31‰ salinity (S)] were acclimated to a dilute medium (15‰ S) for 10 days, employing silver staining to locate gill ion transporting tissue, immunofluorescence to localize the Na/K-ATPase α-subunit in the lamellae, and electron microscopy to portray ultrastructural changes in the gill epithelia. Na/K-ATPase activity was characterized kinetically in a gill microsomal fraction, including synergistic stimulation by NH plus K. Silver staining revealed that all 26 phyllobranchiate arthro- and pleurobranchiae participate in ion transport. Na/K-ATPase α-subunit staining was weak in SW crabs and distributed exclusively and irregularly within the intralamellar septal cells, particularly at the septal-pillar cell body junctions, and septal cell cytoplasm facing the hemolymph space. In 15‰ S crabs, α-subunit localization was intense, occupying the entire thickened septum. Pillar cells and flanges did not stain. Mitochondria and membrane foldings increased in the pillar cell flanges and intralamellar septal cells, greatly amplifying surface area. Only a single ATP binding site (V = 130.8 ± 10.5 nmol min mg protein; K = 55.3 ± 1.7 μmol l) obeying Michaelis-Menten kinetics was disclosed. Na/K-ATPase activity was modulated by Mg, Na, and NH, exhibiting site-site interactions; K modulation showed Michaelis-Menten kinetics. K plus NH synergistically stimulated activity ≈ 1.7-fold. Ouabain inhibited total ATPase activity by ≈ 70% (K = 220-300 μmol l), revealing phosphohydrolytic activities other than the Na/K-ATPase. Despite ample phylogenetic separation, the phyllobranchiate lamellae of the Anomura and Caridea share many ultrastructural features, that is, an intralamellar septum and opposed abutting pillar cells, similar Na/K-ATPase distribution, and comparable kinetic characteristics. These findings suggest either convergent evolution at the structural and biochemical levels, or preservation of traits present in a remote common ancestor.
新鲜捕获的 Clibanarius vittatus [SW,31‰盐度(S)]被适应于稀释介质(15‰ S)10 天,采用银染定位鳃离子转运组织,免疫荧光定位板层中的 Na/K-ATPase α-亚基,并通过电子显微镜描绘鳃上皮的超微结构变化。Na/K-ATPase 活性在鳃微粒体部分中通过动力学进行特征描述,包括 NH 和 K 的协同刺激。银染显示所有 26 个叶状鳃和胸肢都参与离子转运。SW 螃蟹的 Na/K-ATPase α-亚基染色较弱,仅在板层隔细胞内分布且不均匀,特别是在隔柱细胞体连接处和隔细胞细胞质面向血腔空间。在 15‰ S 螃蟹中,α-亚基定位强烈,占据整个增厚的隔。柱细胞和翼部不染色。线粒体和膜折叠在柱细胞翼部和板层隔细胞中增加,大大增加了表面积。仅披露了一个单一的 ATP 结合位点(V = 130.8 ± 10.5 nmol min mg 蛋白;K = 55.3 ± 1.7 μmol l),符合米氏动力学。Na/K-ATPase 活性受 Mg、Na 和 NH 调节,表现出位点-位点相互作用;K 调节显示米氏动力学。K 和 NH 协同刺激活性增加约 1.7 倍。哇巴因抑制总 ATP 酶活性约 70%(K = 220-300 μmol l),揭示了除 Na/K-ATPase 以外的磷酸水解活性。尽管有充分的系统发育分离,但 Anomura 和 Caridea 的叶状板层具有许多超微结构特征,即板层隔和相对的毗邻柱细胞,相似的 Na/K-ATPase 分布和可比的动力学特征。这些发现表明在结构和生化水平上存在趋同进化,或者保留了在遥远的共同祖先中存在的特征。