Urinary concentrating defect in mice lacking Epac1 or Epac2. Issue 2 (25th September 2018)
- Record Type:
- Journal Article
- Title:
- Urinary concentrating defect in mice lacking Epac1 or Epac2. Issue 2 (25th September 2018)
- Main Title:
- Urinary concentrating defect in mice lacking Epac1 or Epac2
- Authors:
- Cherezova, Alena
Tomilin, Viktor
Buncha, Vadym
Zaika, Oleg
Ortiz, Pablo A.
Mei, Fang
Cheng, Xiaodong
Mamenko, Mykola
Pochynyuk, Oleh - Abstract:
- ABSTRACT: cAMP is a universal second messenger regulating a plethora of processes in the kidney. Two downstream effectors of cAMP are PKA and exchange protein directly activated by cAMP (Epac), which, unlike PKA, is often linked to elevation of [Ca 2+ ]i . While both Epac isoforms (Epac1 and Epac2) are expressed along the nephron, their relevance in the kidney remains obscure. We combined ratiometric calcium imaging with quantitative immunoblotting, immunofluorescent confocal microscopy, and balance studies in mice lacking Epac1 or Epac2 to determine the role of Epac in renal water‐solute handling. Epac1 −/− and Epac2 −/− mice developed polyuria despite elevated arginine vasopressin levels. We did not detect major deficiencies in arginine vasopressin [Ca 2+ ]i signaling in split‐opened collecting ducts or decreases in aquaporin water channel type 2 levels. Instead, sodium‐hydrogen exchanger type 3 levels in the proximal tubule were dramatically reduced in Epac1 −/− and Epac2 −/− mice. Water deprivation revealed persisting polyuria, impaired urinary concentration ability, and augmented urinary excretion of Na + and urea in both mutant mice. In summary, we report a nonredundant contribution of Epac isoforms to renal function. Deletion of Epac1 and Epac2 decreases sodium–hydrogen exchanger type 3 expression in the proximal tubule, leading to polyuria and osmotic diuresis.—Cherezova, A., Tomilin, V., Buncha, V., Zaika, O., Ortiz, P. A., Mei, F., Cheng, X., Mamenko, M.,ABSTRACT: cAMP is a universal second messenger regulating a plethora of processes in the kidney. Two downstream effectors of cAMP are PKA and exchange protein directly activated by cAMP (Epac), which, unlike PKA, is often linked to elevation of [Ca 2+ ]i . While both Epac isoforms (Epac1 and Epac2) are expressed along the nephron, their relevance in the kidney remains obscure. We combined ratiometric calcium imaging with quantitative immunoblotting, immunofluorescent confocal microscopy, and balance studies in mice lacking Epac1 or Epac2 to determine the role of Epac in renal water‐solute handling. Epac1 −/− and Epac2 −/− mice developed polyuria despite elevated arginine vasopressin levels. We did not detect major deficiencies in arginine vasopressin [Ca 2+ ]i signaling in split‐opened collecting ducts or decreases in aquaporin water channel type 2 levels. Instead, sodium‐hydrogen exchanger type 3 levels in the proximal tubule were dramatically reduced in Epac1 −/− and Epac2 −/− mice. Water deprivation revealed persisting polyuria, impaired urinary concentration ability, and augmented urinary excretion of Na + and urea in both mutant mice. In summary, we report a nonredundant contribution of Epac isoforms to renal function. Deletion of Epac1 and Epac2 decreases sodium–hydrogen exchanger type 3 expression in the proximal tubule, leading to polyuria and osmotic diuresis.—Cherezova, A., Tomilin, V., Buncha, V., Zaika, O., Ortiz, P. A., Mei, F., Cheng, X., Mamenko, M., Pochynyuk, O. Urinary concentrating defect in mice lacking Epac1 or Epac2. FASEB J. 33, 2156–2170 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 2(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 2(2019)
- Issue Display:
- Volume 33, Issue 2 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 2
- Issue Sort Value:
- 2019-0033-0002-0000
- Page Start:
- 2156
- Page End:
- 2170
- Publication Date:
- 2018-09-25
- Subjects:
- collecting duct -- AQP2 -- NHE-3 -- urea -- water deprivation
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201800435R ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13220.xml