PUBLICATION
            Specific Expression and Regulation of Glucose Transporters in Zebrafish Ionocytes
- Authors
 - Tseng, Y.C., Chen, R.D., Lee, J.R., Liu, S.T., Lee, S.J., and Hwang, P.P.
 - ID
 - ZDB-PUB-090526-25
 - Date
 - 2009
 - Source
 - American journal of physiology. Regulatory, integrative and comparative physiology 297(2): R275-R290 (Journal)
 - Registered Authors
 - Hwang, Pung Pung, Lee, Shyh-Jye, Tseng, Yung-Che
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Epithelial Cells/metabolism*
 - Animals
 - Protein Isoforms/genetics
 - Chlorides/pharmacology
 - Glucose Transport Proteins, Facilitative/chemistry
 - Glucose Transport Proteins, Facilitative/genetics
 - Glucose Transport Proteins, Facilitative/metabolism*
 - Acclimatization/genetics
 - Molecular Sequence Data
 - Oligonucleotides, Antisense/genetics
 - Sodium/pharmacology
 - Amino Acid Sequence
 - Protein Structure, Tertiary/genetics
 - Zebrafish/genetics
 - Zebrafish/metabolism*
 - Gene Expression Regulation, Developmental/physiology
 - Gene Order/genetics
 - Membrane Proteins/chemistry
 - Gills/cytology*
 - Gills/metabolism
 - Skin/metabolism
 - Cloning, Molecular
 - Gene Expression Regulation*
 - Forkhead Transcription Factors/genetics
 - Larva/metabolism
 - DNA, Complementary/genetics
 - Animal Structures/metabolism
 - Sequence Homology, Amino Acid
 - Gene Expression/drug effects
 - Gene Expression/genetics
 - Calcium/pharmacology
 - Phylogeny
 - Zebrafish Proteins/chemistry
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/metabolism*
 
 - PubMed
 - 19458281 Full text @ Am. J. Physiol. Regul. Integr. Comp. Physiol.
 
            Citation
        
        
            Tseng, Y.C., Chen, R.D., Lee, J.R., Liu, S.T., Lee, S.J., and Hwang, P.P. (2009) Specific Expression and Regulation of Glucose Transporters in Zebrafish Ionocytes. American journal of physiology. Regulatory, integrative and comparative physiology. 297(2):R275-R290.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Glucose, a carbohydrate metabolite, plays a major role in the energy supply for fish iono- and osmoregulation, and the way that glucose is transported in ionocytes is a critical process related to the functional operations of ionocytes. Eighteen members of glucose transporters (GLUTs, SLC2A) were cloned and identified from zebrafish. Previously, Na(+),K(+)-ATPase-rich (NaR), Na(+)-Cl(-) cotransporter-expressing (NCC), H(+)-ATPase-rich (HR), and glycogen-rich (GR) cells have identified to be responsible for Ca(2+) uptake, Cl(-) uptake, Na(+) uptake, and the energy deposition, respectively, in zebrafish skin/gills. The purpose of the present study was to test the hypothesis of whether GLUT isoforms are specifically expressed and function in ionocytes to supply energy for ion regulatory mechanisms. Based on translational knockdown of foxi3a/3b (2 transcriptional factors related to the ionocytes' differentiation) and triple in situ hybridization/immunocytochemistry, 3 GLUT isoforms, zglut1a, -6, and -13.1, were specifically localized in NaR/NCC cells, GR cells, and HR cells, respectively. mRNA expression of zglut1a in embryos and adult gills were stimulated by the low Ca(2+) or low Cl(-) freshwater, which has been previously reported to respectively upregulate the functions (monitored by epithelial Ca(2+) channel, NCC mRNA) of NaR/NCC cells, while that of zglut13.1 was stimulated only by low Na(+), a situation to upregulate the function (monitored by carbonic anhydrase 15a mRNA) of HR cells. On the other hand, ambient ion compositions did not affect the zglut6 mRNA expression. Taken together, zGLUT1a, -6, and 13.1, the specific transporters in NaR/NCC cells, GR cells, and HR cells, may absorb glucose into the respective cells to fulfill different physiological demands. Key words: mitochondrion-rich cells, ion transport, environment, adaptation, epithelium.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping