PUBLICATION

Aquaporin 1 Is Involved in Acid Secretion by Ionocytes of Zebrafish Embryos through Facilitating CO2 Transport

Authors
Horng, J.L., Chao, P.L., Chen, P.Y., Shih, T.H., Lin, L.Y.
ID
ZDB-PUB-150820-2
Date
2015
Source
PLoS One   10: e0136440 (Journal)
Registered Authors
Keywords
Embryos, Secretion, Zebrafish, Carbon dioxide, Gills, Cell membranes, In situ hybridization, Morpholino
MeSH Terms
  • Acids/metabolism
  • Animals
  • Aquaporin 1/antagonists & inhibitors
  • Aquaporin 1/genetics
  • Aquaporin 1/metabolism*
  • Carbon Dioxide/metabolism*
  • Gene Knockdown Techniques
  • Immunohistochemistry
  • In Situ Hybridization
  • Proton-Translocating ATPases/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Real-Time Polymerase Chain Reaction
  • Skin/cytology
  • Skin/metabolism
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish/metabolism*
  • Zebrafish Proteins/antagonists & inhibitors
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed
26287615 Full text @ PLoS One
Abstract
Mammalian aquaporin 1 (AQP1) is well known to function as a membrane channel for H2O and CO2 transport. Zebrafish AQP1a.1 (the homologue of mammalian AQP1) was recently identified in ionocytes of embryos; however its role in ionocytes is still unclear. In this study, we hypothesized that zebrafish AQP1a.1 is involved in the acid secretion by ionocytes through facilitating H2O and CO2 diffusion. A real-time PCR showed that mRNA levels of AQP1a.1 in embryos were induced by exposure to 1% CO2 hypercapnia for 3 days. In situ hybridization and immunohistochemistry showed that the AQP1a.1 transcript was highly expressed by acid-secreting ionocytes, i.e., H+-ATPase-rich (HR) cells. A scanning ion-selective electrode technique (SIET) was applied to analyze CO2-induced H+ secretion by individual ionocytes in embryos. H+ secretion by HR cells remarkably increased after a transient loading of CO2 (1% for 10 min). AQP1a.1 knockdown with morpholino oligonucleotides decreased the H+ secretion of HR cells by about half and limited the CO2 stimulated increase. In addition, exposure to an AQP inhibitor (PCMB) for 10 min also suppressed CO2-induced H+ secretion. Results from this study support our hypothesis and provide in vivo evidence of the physiological role of AQP1 in CO2 transport.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping