Am J Physiol Cell Physiol 285: C205-C214, 2003.
First published March 26, 2003; doi:10.1152/ajpcell.00008.2003
0363-6143/03 $5.00
MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS
pH of TGN and recycling endosomes of H+/K+-ATPase-transfected HEK-293 cells: implications for pH regulation in the secretory pathway
Terry E. Machen,1
Mary Jae Leigh,1
Carmen Taylor,1,3
Tohru Kimura,2
Shinji Asano,2 and
Hsiao-Ping H. Moore1
1Department of Molecular and Cell Biology, University of California, Berkeley,
California 94720-3200; 2Molecular Genetics Research Center, Toyama Medical and Pharmaceutical University, Toyama City, Toyama 930-0194, Japan; and 3Graduate Group in Bioengineering, University of California, Berkeley,
Calilfornia 94720-1762
Submitted 9 January 2003
; accepted in final form 13 March 2003
The influences of the gastric H+/K+ pump on organelle
pH during trafficking to and from the plasma membrane were investigated using
HEK-293 cells stably expressing the
- and
-subunits of human
H+/K+-ATPase (H+/K+-
,
cells). The pH values of trans-Golgi network (pHTGN) and
recycling endosomes (pHRE) were measured by transfecting
H+/K+-
,
cells with the pH-sensitive GFP
pHluorin fused to targeting sequences of either TGN38 or synaptobrevin,
respectively. Immunofluorescence showed that
H+/K+-ATPase was present in the plasma membrane, TGN,
and RE. The pHTGN was similar in both
H+/K+-
,
cells (pHTGN 6.36) and
vector-transfected ("mock") cells (pHTGN 6.34);
pHRE was also similar in H+/K+-
,
(pHRE 6.40) and mock cells (pHRE 6.37). SCH28080
(inhibits H+/K+-ATPase) caused TGN to alkalinize by 0.12
pH units; subsequent addition of bafilomycin (inhibits H+ v-ATPase)
caused TGN to alkalinize from pH 6.4 up to a new steady-state pHTGN
of 7.07.5, close to pHcytosol. Similar results were observed
in RE. Thus H+/K+-ATPases that trafficked to the plasma
membrane were active but had small effects to acidify the TGN and RE compared
with H+ v-ATPase. Mathematical modeling predicted a large number of
H+ v-ATPases (8,000) active in the TGN to balance a large, passive
H+ leak (with PH
103 cm/s) via unidentified pathways out of
the TGN. We propose that in the presence of this effective, though
inefficient, buffer system in the Golgi and TGN,
H+/K+-ATPases (estimated to be
4,000 active in the
TGN) and other transporters have little effect on luminal pH as they traffic
to the plasma membrane.
pHluorin; H+ v-ATPase; trans-Golgi network; organelle pH; H+ permeability
Address for reprint requests and other correspondence: T. E. Machen, 231 LSA,
Dept of Molecular and Cell Biology, Univ. of California - Berkeley, Berkeley,
CA 94720-3200 (E-mail:
machen{at}socrates.berkeley.edu).
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Copyright © 2003 by the American Physiological Society.