4.3 Article

Prolactin 177, prolactin 188, and extracellular osmolality independently regulate the gene expression of ion transport effectors in gill of Mozambique tilapia

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00168.2015

关键词

ionocytes; prolactin; extracellular osmolality; tilapia

资金

  1. National Science Foundation (NSF) [IOS-1119693]
  2. Edwin W. Pauley Foundation
  3. Binational Agricultural Research Development (BARD) fund [IS-4296-10]
  4. National Oceanic and Atmospheric Administration [NA14OAR4170071]
  5. University of Hawaii Sea Grant College Program, SOEST [R/SS-12]
  6. University of Hawaii NSF EPSCoR program [EPS-0903833]
  7. Core Genetics Facility at the Hawaii Institute of Marine Biology, University of Hawaii
  8. Research Fellow of Japan Society for the Promotion of Science [2440164]
  9. University of Hawaii Sea Grant [UNIHI-SEAGRANT-JC-14-23]
  10. Grants-in-Aid for Scientific Research [26252032, 15J07266] Funding Source: KAKEN

向作者/读者索取更多资源

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 alpha 1a (NKA alpha 1a) 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 (tPRL(177) and tPRL(188)). oPRL and the two native tPRLs showed concentration-dependent effects on NCC, NKA alpha 1a, 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.

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