期刊
JOURNAL OF PHYSIOLOGY-LONDON
卷 568, 期 2, 页码 445-458出版社
BLACKWELL PUBLISHING
DOI: 10.1113/jphysiol.2005.092957
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Cell migration is crucial for immune defence, wound healing or formation of tumour metastases. it has been shown that the activity of the Na+-H+ exchanger (NHEI) plays an important role in cell migration. However, so far it is unknown whether Na+-HCO3 cotransport (NBC), which has similar functions in the regulation of intracellular pH (pH(i)) as NHEI, is also involved in cell migration. We therefore isolated NHE-deficient Madin-Darby canine kidney (MDCK-F) cells and tested whether NBC compensates for NHE in pH(i) and cell volume regulation as well as in migration. Intracellular pH was measured with the fluorescent pH indicator 2'7'-bis(carboxyethyl)-5-carboxyfluorescein (BCECF). The expression of NBC isoforms was determined with semiquantitative PCR. Migration was monitored with time-lapse video microscopy and quantified as the displacement of the cell centre. We found that MDCK-F cells express the isoform NBC1 (SLCA4A gene product) at a much higher level than the isoform kNBC3 (SLCA4A8 gene product). This difference is even more pronounced in NHE-deficient cells so that NBC1 is likely to be the major acid extruder in these cells and the major mediator of propionate-induced cell volume increase. NHE-deficient MDCK-F cells migrate more slowly than normal MDCK-F cells. NBC activity promotes migration during an acute intracellular acid load and increases migratory speed and displacement on a short timescale (< 30 min) whereas it has no effect on the long-term behaviour of migrating MDCK-F cells. Taken together, our results show that NBC actvity, despite many functional similarities, does not have the same importance for cell migration as NHE1 activity.
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