Advertisement
Research Article Free access | 10.1172/JCI116367
Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205.
Find articles by Uchida, S. in: JCI | PubMed | Google Scholar
Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205.
Find articles by Yamauchi, A. in: JCI | PubMed | Google Scholar
Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205.
Find articles by Preston, A. in: JCI | PubMed | Google Scholar
Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205.
Find articles by Kwon, H. in: JCI | PubMed | Google Scholar
Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205.
Find articles by Handler, J. in: JCI | PubMed | Google Scholar
Published April 1, 1993 - More info
Betaine is one of the major compatible osmolytes accumulated by kidney derived Madin-Darby canine kidney cells cultured in hypertonic medium. Betaine is accumulated by Na(+)- and Cl(-)-dependent uptake from the medium. To gain insight into the mechanism by which hypertonicity evokes an increase in the Vmax of the betaine transporter in Madin-Darby canine kidney cells, we measured the relative abundance of mRNA for the transporter in cells shifted to a hypertonic medium and found parallel increases in mRNA abundance and cotransporter activity. The increase in mRNA levels preceded the increase in transporter activity slightly. Transcription of the gene for the transporter rose rapidly and to the same relative extent as mRNA abundance in cells shifted to hypertonic medium, indicating that transcription of the gene for the cotransporter plays a major role in regulating the accumulation of betaine in response to hypertonicity.
Images.
Click on an image below to see the page. View PDF of the complete article