Microtubule-dependent relocation of branchial V-H+-ATPase to the basolateral membrane in the Pacific spiny dogfish (Squalus acanthias): a role in base secretion
- PMID: 16449555
- DOI: 10.1242/jeb.02059
Microtubule-dependent relocation of branchial V-H+-ATPase to the basolateral membrane in the Pacific spiny dogfish (Squalus acanthias): a role in base secretion
Abstract
We have previously shown that continuous intravenous infusion of NaHCO3 for 24 h ( approximately 1000 micromol kg(-1) h(-1)) results in the relocation of V-H+-ATPase from the cytoplasm to the basolateral membrane in the gills of the Pacific dogfish. To further investigate this putative base-secretive process we performed similar experiments with the addition of colchicine, an inhibitor of cytoskeleton-dependent cellular trafficking processes. Blood pH and plasma total CO2 were significantly higher in the colchicines-treated, HCO3- -infused fish compared with fish infused with HCO3- alone. The effect of colchicine was highest after 24 h of infusion (8.33+/-0.06 vs 8.02+/-0.03 pH units, 15.72+/-3.29 vs 6.74+/-1.34 mmol CO2 l(-1), N=5). Immunohistochemistry and western blotting confirmed that colchicine blocked the transit of V-H+-ATPase to the basolateral membrane. Furthermore, western blotting analyses from whole gill and cell membrane samples suggest that the short-term (6 h) response to alkaline stress consists of relocation of V-H+-ATPases already present in the cell to the basolateral membrane, while in the longer term (24 h) there is both relocation of preexistent enzyme and upregulation in the synthesis of new units. Our results strongly suggest that cellular relocation of V-H+-ATPase is necessary for enhanced HCO3- secretion across the gills of the Pacific dogfish.
Similar articles
-
Regulation of branchial V-H(+)-ATPase, Na(+)/K(+)-ATPase and NHE2 in response to acid and base infusions in the Pacific spiny dogfish (Squalus acanthias).J Exp Biol. 2005 Jan;208(Pt 2):345-54. doi: 10.1242/jeb.01382. J Exp Biol. 2005. PMID: 15634853
-
Recovery from blood alkalosis in the Pacific hagfish (Eptatretus stoutii): involvement of gill V-H+-ATPase and Na+/K+-ATPase.Comp Biochem Physiol A Mol Integr Physiol. 2007 Sep;148(1):133-41. doi: 10.1016/j.cbpa.2007.03.032. Epub 2007 Apr 18. Comp Biochem Physiol A Mol Integr Physiol. 2007. PMID: 17512231
-
V-H+ -ATPase translocation during blood alkalosis in dogfish gills: interaction with carbonic anhydrase and involvement in the postfeeding alkaline tide.Am J Physiol Regul Integr Comp Physiol. 2007 May;292(5):R2012-9. doi: 10.1152/ajpregu.00814.2006. Epub 2007 Jan 4. Am J Physiol Regul Integr Comp Physiol. 2007. PMID: 17204588
-
Vacuolar H(+)-ATPase in the kidney.J Nephrol. 2002 Mar-Apr;15 Suppl 5:S22-31. J Nephrol. 2002. PMID: 12027218 Review.
-
Acid-base balance and CO2 excretion in fish: unanswered questions and emerging models.Respir Physiol Neurobiol. 2006 Nov;154(1-2):199-215. doi: 10.1016/j.resp.2006.04.010. Epub 2006 Jun 13. Respir Physiol Neurobiol. 2006. PMID: 16777496 Review.
Cited by
-
Bicarbonate-sensing soluble adenylyl cyclase is present in the cell cytoplasm and nucleus of multiple shark tissues.Physiol Rep. 2017 Jan;5(2):e13090. doi: 10.14814/phy2.13090. Physiol Rep. 2017. PMID: 28108644 Free PMC article.
-
Inhibitors of the V0 subunit of the vacuolar H+-ATPase prevent segregation of lysosomal- and secretory-pathway proteins.J Cell Sci. 2009 Oct 1;122(Pt 19):3542-53. doi: 10.1242/jcs.034298. Epub 2009 Sep 8. J Cell Sci. 2009. PMID: 19737820 Free PMC article.
-
The role of cAMP-mediated intracellular signaling in regulating Na+ uptake in zebrafish larvae.Am J Physiol Regul Integr Comp Physiol. 2014 Jan 1;306(1):R51-60. doi: 10.1152/ajpregu.00317.2013. Epub 2013 Nov 20. Am J Physiol Regul Integr Comp Physiol. 2014. PMID: 24259461 Free PMC article.
-
Development in a naturally acidified environment: Na+/H+-exchanger 3-based proton secretion leads to CO2 tolerance in cephalopod embryos.Front Zool. 2013 Aug 29;10(1):51. doi: 10.1186/1742-9994-10-51. Front Zool. 2013. PMID: 23988184 Free PMC article.
-
How to get into bones: proton pump and carbonic anhydrase in Osedax boneworms.Proc Biol Sci. 2013 May 1;280(1761):20130625. doi: 10.1098/rspb.2013.0625. Print 2013 Jun 22. Proc Biol Sci. 2013. PMID: 23760644 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources