Inokuchi Mayu, Breves Jason P, Moriyama Shunsuke, Watanabe Soichi, Kaneko Toyoji, Lerner Darren T, Grau E Gordon, Seale Andre P
Hawaii Institute of Marine Biology, University of Hawaii, Kaneohe, Hawaii; Department of Aquatic Bioscience, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan; and
Department of Biology, Skidmore College, Saratoga Springs, New York;
Am J Physiol Regul Integr Comp Physiol. 2015 Nov 15;309(10):R1251-63. doi: 10.1152/ajpregu.00168.2015. Epub 2015 Sep 16.
This study characterized the local effects of extracellular osmolality and prolactin (PRL) on branchial ionoregulatory function of a euryhaline teleost, Mozambique tilapia (Oreochromis mossambicus). First, gill filaments were dissected from freshwater (FW)-acclimated tilapia and incubated in four different osmolalities, 280, 330, 380, and 450 mosmol/kg H2O. The mRNA expression of Na(+)/K(+)-ATPase α1a (NKA α1a) and Na(+)/Cl(-) cotransporter (NCC) showed higher expression with decreasing media osmolalities, while Na(+)/K(+)/2Cl(-) cotransporter 1a (NKCC1a) and PRL receptor 2 (PRLR2) mRNA levels were upregulated by increases in media osmolality. We then incubated gill filaments in media containing ovine PRL (oPRL) and native tilapia PRLs (tPRL177 and tPRL188). oPRL and the two native tPRLs showed concentration-dependent effects on NCC, NKAα1a, and PRLR1 expression; Na(+)/H(+) exchanger 3 (NHE3) expression was increased by 24 h of incubation with tPRLs. Immunohistochemical observation showed that oPRL and both tPRLs maintained a high density of NCC- and NKA-immunoreactive ionocytes in cultured filaments. Furthermore, we found that tPRL177 and tPRL188 differentially induce expression of these ion transporters, according to incubation time. Together, these results provide evidence that ionocytes of Mozambique tilapia may function as osmoreceptors, as well as directly respond to PRL to modulate branchial ionoregulatory functions.
本研究表征了细胞外渗透压和催乳素(PRL)对广盐性硬骨鱼莫桑比克罗非鱼(Oreochromis mossambicus)鳃离子调节功能的局部影响。首先,从适应淡水(FW)的罗非鱼身上解剖出鳃丝,并在四种不同渗透压(280、330、380和450 mosmol/kg H2O)下进行孵育。Na(+)/K(+)-ATP酶α1a(NKA α1a)和Na(+)/Cl(-)共转运体(NCC)的mRNA表达随着培养基渗透压的降低而升高,而Na(+)/K(+)/2Cl(-)共转运体1a(NKCC1a)和催乳素受体2(PRLR2)的mRNA水平则随着培养基渗透压的升高而上调。然后,我们将鳃丝在含有绵羊催乳素(oPRL)和天然罗非鱼催乳素(tPRL177和tPRL188)的培养基中孵育。oPRL和两种天然tPRL对NCC、NKAα1a和PRLR1表达呈现浓度依赖性效应;与tPRL孵育24小时后,Na(+)/H(+)交换体3(NHE3)表达增加。免疫组织化学观察表明,oPRL和两种tPRL在培养的鳃丝中均维持了高密度的NCC和NKA免疫反应性离子细胞。此外,我们发现tPRL177和tPRL188根据孵育时间差异诱导这些离子转运体的表达。总之,这些结果提供了证据,表明莫桑比克罗非鱼的离子细胞可能作为渗透压感受器发挥作用,并直接响应PRL来调节鳃的离子调节功能。