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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 

Expression of aquaporin-3 in human peritoneal mesothelial cells and its up-regulation by glucose in vitro.

BACKGROUND: Aquaporin-3 (AQP3) is a member of the water channel family that is selective for the passage of not only water, but also glycerol and urea. Our recent study demonstrated the presence of aquaporin-1 in human peritoneal mesothelial cells (HPMC). Although transcripts encoding for AQP3 has been detected by reverse transcription-polymerase chain reaction (RT-PCR) in murine peritoneal mesothelium, to date there is no documentation of protein expression on peritoneal mesothelial cells. METHOD: Our present study was designed to explore the gene and protein expression of AQP3 in HPMC and its regulation under different concentrations of glucose. RESULTS: AQP3 protein was detected in the human peritoneal tissue by immunohistological staining using specific, affinity-purified polyclonal anti-AQP3 antibodies. AQ3 transcripts and protein expression in cultured HPMC were investigated by RT-PCR and immunoblotting analysis respectively. Cell permeability to glycerol (flux) was measured using [(14)C]glycerol incorporation. AQP3 transcript and protein were weakly expressed in HPMC constitutively. The gene expression of AQP3 and its protein biosynthesis in HPMC were inducible following exposure to glucose in a dose- and time-dependent manner (P < 0.0001). Glucose at a concentration of 200 mmol induced glycerol flux by 4.82-fold above the control value (P < 0.0001) and its effect was significantly inhibited by mercuric chloride (P < 0.01). CONCLUSION: Our novel observation demonstrated the AQP3 expression and biosynthesis in HPMC and in vitro studies revealed that glycerol permeability in HPMC was up-regulated by glucose. Further study is warranted to elucidate the role of AQP3 in HPMC for maintaining the ultrafiltration of the peritoneal membrane.[1]

References

  1. Expression of aquaporin-3 in human peritoneal mesothelial cells and its up-regulation by glucose in vitro. Lai, K.N., Leung, J.C., Chan, L.Y., Tang, S., Li, F.K., Lui, S.L., Chan, T.M. Kidney Int. (2002) [Pubmed]
 
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