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Membrane water permeability and aquaporin expression increase during growth of maize suspension cultured cells
Author(s) -
MOSHELION MENACHEM,
HACHEZ CHARLES,
YE QING,
CAVEZ DAMIEN,
BAJJI MOHAMMED,
JUNG RUDOLF,
CHAUMONT FRANÇOIS
Publication year - 2009
Publication title -
plant, cell and environment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.646
H-Index - 200
eISSN - 1365-3040
pISSN - 0140-7791
DOI - 10.1111/j.1365-3040.2009.02001.x
Subject(s) - aquaporin , gene expression , membrane , permeability (electromagnetism) , biology , protoplast , membrane permeability , aquaporin 2 , messenger rna , chemistry , microbiology and biotechnology , gene , water channel , biochemistry , engineering , mechanical engineering , inlet
Aquaporins (AQPs) are water channels that allow cells to rapidly alter their membrane water permeability. A convenient model for studying AQP expression and activity regulation is Black Mexican Sweet (BMS) maize cultured cells. In an attempt to correlate membrane osmotic water permeability coefficient (P f ) with AQP gene expression, we first examined the expression pattern of 33 AQP genes using macro‐array hybridization. We detected the expression of 18 different isoforms representing the four AQP subfamilies, i.e. eight plasma membrane (PIP), five tonoplast (TIP), three small basic (SIP) and two NOD26‐like (NIP) AQPs. While the expression of most of these genes was constant throughout all growth phases, mRNA levels of ZmPIP1;3 , ZmPIP2;1 , ZmPIP2;2, ZmPIP2;4 and ZmPIP2;6 increased significantly during the logarithmic growth phase and the beginning of the stationary phase. The use of specific anti‐ZmPIP antisera showed that the protein expression pattern correlated well with mRNA levels. Cell pressure probe and protoplast swelling measurements were then performed to determine the P f . Interestingly, we found that the P f were significantly increased at the end of the logarithmic growth phase and during the steady‐state phase compared to the lag phase, demonstrating a positive correlation between AQP abundance in the plasma membrane and the cell P f .