2012
DOI: 10.1002/jcb.24246
|View full text |Cite
|
Sign up to set email alerts
|

Aquaporin 2‐increased renal cell proliferation is associated with cell volume regulation

Abstract: We have previously demonstrated that in renal cortical collecting duct cells (RCCD(1)) the expression of the water channel Aquaporin 2 (AQP2) raises the rate of cell proliferation. In this study, we investigated the mechanisms involved in this process, focusing on the putative link between AQP2 expression, cell volume changes, and regulatory volume decrease activity (RVD). Two renal cell lines were used: WT-RCCD(1) (not expressing aquaporins) and AQP2-RCCD(1) (transfected with AQP2). Our results showed that wh… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
21
0

Year Published

2013
2013
2020
2020

Publication Types

Select...
8
1

Relationship

3
6

Authors

Journals

citations
Cited by 21 publications
(22 citation statements)
references
References 37 publications
1
21
0
Order By: Relevance
“…Indeed, we demonstrated a few years ago that, in native, isolated perfused, CCDs, induction of PCs to swell by current transfer techniques was immediately followed by cell volume regulation back to control volume states, a process that was dependent upon the Ba 2+ -sensitive apical K + channels [85] that would include ROMK and all K Ca channels. Others have shown that CCD cells in culture undergo regulatory volume decrease upon cell swelling [86] and that cell swelling activates TRP channels to induce Ca 2+ influx in collecting duct cells [43], [86], [87]. Since we have also shown that, in M-1 cells, cell swelling activates TRPV4 and Ca 2+ influx which, in turn, leads to activation of both BK and SK3, it seems reasonable to conclude that swelling states in native CCD and CNT, at least for PCs, leads to activation of both BK and SK3 to effect cell volume regulation.…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, we demonstrated a few years ago that, in native, isolated perfused, CCDs, induction of PCs to swell by current transfer techniques was immediately followed by cell volume regulation back to control volume states, a process that was dependent upon the Ba 2+ -sensitive apical K + channels [85] that would include ROMK and all K Ca channels. Others have shown that CCD cells in culture undergo regulatory volume decrease upon cell swelling [86] and that cell swelling activates TRP channels to induce Ca 2+ influx in collecting duct cells [43], [86], [87]. Since we have also shown that, in M-1 cells, cell swelling activates TRPV4 and Ca 2+ influx which, in turn, leads to activation of both BK and SK3, it seems reasonable to conclude that swelling states in native CCD and CNT, at least for PCs, leads to activation of both BK and SK3 to effect cell volume regulation.…”
Section: Discussionmentioning
confidence: 99%
“…According to the phylogenetic analysis of Johanson and Gustavsson [18], plant aquaporins are classified into four main subfamilies, widely distributed among higher plants: PIPs (plasma membrane intrinsic proteins), TIPs (tonoplast intrinsic proteins), SIPs (small basic intrinsic proteins), and NIPs (26 kDa intrinsic proteins). The aquaporins are presently and extensively studied, since their importance spans from animal [19] and human physiology [20] to osmo-adaptation of microorganisms [21] and vegetables [22, 23]. The transcripts encoding sugarcane aquaporins have only marginally been described, despite their significant physiological influence and participation in several processes during plant growth and acclimation against biotic and abiotic stresses [24, 25].…”
Section: Introductionmentioning
confidence: 99%
“…Due to the sub-second resolution of our method we cannot compare our findings directly with the available literature since both experimental and theoretical approaches involve slow exchange processes or steady state modeling [23,24,25,26]. However, as far as the trafficking of AQP2 is concerned it has already been reported in CD8 cells ( in vitro system as opposed to our ex vivo system) that hypotonic challenge induces internalization of AQP2 [20].…”
Section: Discussionmentioning
confidence: 39%