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  1. Article ; Online: Kinase Scaffold Cab39 Is Necessary for Phospho-Activation of the Thiazide-Sensitive NCC.

    Ferdaus, Mohammed Z / Koumangoye, Rainelli B / Welling, Paul A / Delpire, Eric

    Hypertension (Dallas, Tex. : 1979)

    2024  Volume 81, Issue 4, Page(s) 801–810

    Abstract: Background: Potassium regulates the WNK (with no lysine kinase)-SPAK (STE20/SPS1-related proline/alanine-rich kinase) signaling axis, which in turn controls the phosphorylation and activation of the distal convoluted tubule thiazide-sensitive NCC ( ... ...

    Abstract Background: Potassium regulates the WNK (with no lysine kinase)-SPAK (STE20/SPS1-related proline/alanine-rich kinase) signaling axis, which in turn controls the phosphorylation and activation of the distal convoluted tubule thiazide-sensitive NCC (sodium-chloride cotransporter) for sodium-potassium balance. Although their roles in the kidney have not been investigated, it has been postulated that Cab39 (calcium-binding protein 39) or Cab39l (Cab39-like) is required for SPAK/OSR1 (oxidative stress response 1) activation. This study demonstrates how they control the WNK-SPAK/OSR1-NCC pathway.
    Methods: We created a global knockout of Cab39l and a tamoxifen-inducible, NCC-driven, Cab39 knockout. The 2 lines were crossed to generate Cab39-DKO (Cab39 double knockout) animals. Mice were studied under control and low-potassium diet, which activates WNK-SPAK/OSR1-NCC phosphorylation. Western blots were used to assess the expression and phosphorylation of proteins. Blood and urine electrolytes were measured to test for compromised NCC function. Immunofluorescence studies were conducted to localize SPAK and OSR1.
    Results: Both Cab39l and Cab39 are expressed in distal convoluted tubule, and only the elimination of both leads to a striking absence of NCC phosphorylation. Cab39-DKO mice exhibited a loss-of-NCC function, like in Gitelman syndrome. In contrast to the apical membrane colocalization of SPAK with NCC in wild-type mice, SPAK and OSR1 become confined to intracellular puncta in the Cab39-DKO mice.
    Conclusions: In the absence of Cab39 proteins, NCC cannot be phosphorylated, resulting in a Gitelman-like phenotype. Cab39 proteins function to localize SPAK at the apical membrane with NCC, reminiscent of the Cab39 yeast homolog function, translocating kinases during cytokinesis.
    MeSH term(s) Mice ; Animals ; Protein Serine-Threonine Kinases/genetics ; Protein Serine-Threonine Kinases/metabolism ; Solute Carrier Family 12, Member 3/genetics ; Solute Carrier Family 12, Member 3/metabolism ; Thiazides/pharmacology ; Phosphorylation ; Kidney Tubules, Distal/metabolism ; Potassium/metabolism
    Chemical Substances Protein Serine-Threonine Kinases (EC 2.7.11.1) ; Solute Carrier Family 12, Member 3 ; Thiazides ; Potassium (RWP5GA015D)
    Language English
    Publishing date 2024-01-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 423736-5
    ISSN 1524-4563 ; 0194-911X ; 0362-4323
    ISSN (online) 1524-4563
    ISSN 0194-911X ; 0362-4323
    DOI 10.1161/HYPERTENSIONAHA.123.22464
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Autosomal dominant PKD gets an atomic map.

    Welling, Paul A

    Nature reviews. Nephrology

    2018  Volume 14, Issue 12, Page(s) 725–726

    MeSH term(s) Humans ; Polycystic Kidney, Autosomal Dominant
    Language English
    Publishing date 2018-10-02
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Comment
    ZDB-ID 2490366-8
    ISSN 1759-507X ; 1759-5061
    ISSN (online) 1759-507X
    ISSN 1759-5061
    DOI 10.1038/s41581-018-0066-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: WNKs on the Fly.

    Welling, Paul A

    Journal of the American Society of Nephrology : JASN

    2018  Volume 29, Issue 5, Page(s) 1347–1349

    MeSH term(s) Animals ; Biological Transport ; Chlorides ; Ion Transport ; Malpighian Tubules ; Signal Transduction
    Chemical Substances Chlorides
    Language English
    Publishing date 2018-04-12
    Publishing country United States
    Document type Editorial ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 1085942-1
    ISSN 1533-3450 ; 1046-6673
    ISSN (online) 1533-3450
    ISSN 1046-6673
    DOI 10.1681/ASN.2018030318
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Roles and Regulation of Renal K Channels.

    Welling, Paul A

    Annual review of physiology

    2016  Volume 78, Page(s) 415–435

    Abstract: More than two dozen types of potassium channels, with different biophysical and regulatory properties, are expressed in the kidney, influencing renal function in many important ways. Recently, a confluence of discoveries in areas from human genetics to ... ...

    Abstract More than two dozen types of potassium channels, with different biophysical and regulatory properties, are expressed in the kidney, influencing renal function in many important ways. Recently, a confluence of discoveries in areas from human genetics to physiology, cell biology, and biophysics has cast light on the special function of five different potassium channels in the distal nephron, encoded by the genes KCNJ1, KCNJ10, KCNJ16, KCNMA1, and KCNN3. Research aimed at understanding how these channels work in health and go awry in disease has transformed our understanding of potassium balance and provided new insights into mechanisms of renal sodium handling and the maintenance of blood pressure. This review focuses on recent advances in this rapidly evolving field.
    MeSH term(s) Animals ; Humans ; Kidney Tubules, Distal/physiology ; Potassium/metabolism ; Potassium Channels/metabolism
    Chemical Substances Potassium Channels ; Potassium (RWP5GA015D)
    Language English
    Publishing date 2016
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 207933-1
    ISSN 1545-1585 ; 0066-4278
    ISSN (online) 1545-1585
    ISSN 0066-4278
    DOI 10.1146/annurev-physiol-021115-105423
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Potassium-Switch Signaling Pathway Dictates Acute Blood Pressure Response to Dietary Potassium.

    Welling, Paul A / Little, Robert / Al-Qusairi, Lama / Delpire, Eric / Ellison, David H / Fenton, Robert A / Grimm, P Richard

    Hypertension (Dallas, Tex. : 1979)

    2024  Volume 81, Issue 5, Page(s) 1044–1054

    Abstract: Background: Potassium (K: Methods: To test the hypothesis that small, physiological changes in plasma K: Results: As P: Conclusions: Low ... ...

    Abstract Background: Potassium (K
    Methods: To test the hypothesis that small, physiological changes in plasma K
    Results: As P
    Conclusions: Low K
    MeSH term(s) Animals ; Mice ; Potassium/metabolism ; Protein Serine-Threonine Kinases/metabolism ; Potassium, Dietary/metabolism ; Blood Pressure/physiology ; Sodium Chloride/metabolism ; Solute Carrier Family 12, Member 3/metabolism ; Signal Transduction ; Phosphorylation ; Kidney Tubules, Distal/metabolism ; Hydrochlorothiazide ; Sodium/metabolism ; Alanine/metabolism ; Proline/metabolism
    Chemical Substances Potassium (RWP5GA015D) ; Protein Serine-Threonine Kinases (EC 2.7.11.1) ; Potassium, Dietary ; Sodium Chloride (451W47IQ8X) ; Solute Carrier Family 12, Member 3 ; Hydrochlorothiazide (0J48LPH2TH) ; Sodium (9NEZ333N27) ; Alanine (OF5P57N2ZX) ; Proline (9DLQ4CIU6V)
    Language English
    Publishing date 2024-03-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 423736-5
    ISSN 1524-4563 ; 0194-911X ; 0362-4323
    ISSN (online) 1524-4563
    ISSN 0194-911X ; 0362-4323
    DOI 10.1161/HYPERTENSIONAHA.123.22546
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Insights into Salt Handling and Blood Pressure. Reply.

    Ellison, David H / Welling, Paul

    The New England journal of medicine

    2022  Volume 386, Issue 7, Page(s) e18

    MeSH term(s) Blood Pressure/physiology ; Humans ; Hypertension/physiopathology ; Sodium Chloride ; Sodium Chloride, Dietary/adverse effects
    Chemical Substances Sodium Chloride, Dietary ; Sodium Chloride (451W47IQ8X)
    Language English
    Publishing date 2022-02-16
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMc2119480
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Low Salt Delivery Triggers Autocrine Release of Prostaglandin E2 From the Aldosterone-Sensitive Distal Nephron in Familial Hyperkalemic Hypertension Mice.

    Zapf, Ava M / Grimm, Paul R / Al-Qusairi, Lama / Delpire, Eric / Welling, Paul A

    Frontiers in physiology

    2022  Volume 12, Page(s) 787323

    Abstract: Aberrant activation of with-no-lysine kinase (WNK)-STE20/SPS1-related proline-alanine-rich protein kinase (SPAK) kinase signaling in the distal convoluted tubule (DCT) causes unbridled activation of the thiazide-sensitive sodium chloride cotransporter ( ... ...

    Abstract Aberrant activation of with-no-lysine kinase (WNK)-STE20/SPS1-related proline-alanine-rich protein kinase (SPAK) kinase signaling in the distal convoluted tubule (DCT) causes unbridled activation of the thiazide-sensitive sodium chloride cotransporter (NCC), leading to familial hyperkalemic hypertension (FHHt) in humans. Studies in FHHt mice engineered to constitutively activate SPAK specifically in the DCT (CA-SPAK mice) revealed maladaptive remodeling of the aldosterone sensitive distal nephron (ASDN), characterized by decrease in the potassium excretory channel, renal outer medullary potassium (ROMK), and epithelial sodium channel (ENaC), that contributes to the hyperkalemia. The mechanisms by which NCC activation in DCT promotes remodeling of connecting tubule (CNT) are unknown, but paracrine communication and reduced salt delivery to the ASDN have been suspected. Here, we explore the involvement of prostaglandin E2 (PGE2). We found that PGE2 and the terminal PGE2 synthase, mPGES1, are increased in kidney cortex of CA-SPAK mice, compared to control or SPAK KO mice. Hydrochlorothiazide (HCTZ) reduced PGE2 to control levels, indicating increased PGE2 synthesis is dependent on increased NCC activity. Immunolocalization studies revealed mPGES1 is selectively increased in the CNT of CA-SPAK mice, implicating low salt-delivery to ASDN as the trigger. Salt titration studies in an
    Language English
    Publishing date 2022-01-06
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2564217-0
    ISSN 1664-042X
    ISSN 1664-042X
    DOI 10.3389/fphys.2021.787323
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Doxycycline Changes the Transcriptome Profile of mIMCD3 Renal Epithelial Cells.

    Jung, Hyun Jun / Coleman, Richard / Woodward, Owen M / Welling, Paul A

    Frontiers in physiology

    2021  Volume 12, Page(s) 771691

    Abstract: Tetracycline-inducible gene expression systems have been used successfully to study gene ... ...

    Abstract Tetracycline-inducible gene expression systems have been used successfully to study gene function
    Language English
    Publishing date 2021-11-05
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2564217-0
    ISSN 1664-042X
    ISSN 1664-042X
    DOI 10.3389/fphys.2021.771691
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: α-Ketoglutarate drives electroneutral NaCl reabsorption in intercalated cells by activating a G-protein coupled receptor, Oxgr1.

    Grimm, Paul R / Welling, Paul A

    Current opinion in nephrology and hypertension

    2017  Volume 26, Issue 5, Page(s) 426–433

    Abstract: Purpose of review: This review describes the recent discoveries about a powerful electroneutral NaCl reabsorption mechanism in intercalated cells, and its regulation by an intrarenal metabolite paracrine, α-ketoglutartate, and the G-protein coupled ... ...

    Abstract Purpose of review: This review describes the recent discoveries about a powerful electroneutral NaCl reabsorption mechanism in intercalated cells, and its regulation by an intrarenal metabolite paracrine, α-ketoglutartate, and the G-protein coupled receptor, Oxgr1.
    Recent findings: The distal nephron fine-tunes sodium, chloride, potassium, hydrogen, bicarbonate and water transport to maintain electrolyte homeostasis and blood pressure. Intercalated cells have been traditionally viewed as the professional regulators of acid-base balance, but recent studies reveal that a specific population of intercalated cells, identified by the pendrin-transporter, have a surprising role in the regulation of salt balance. The pendrin-positive intercalated cells (PP-ICs) facilitate electroneutral NaCl reabsorption through the cooperative activation of multitransport protein network. α-Ketoglutartate is synthesized and secreted into the proximal tubule lumen in the combined state of metabolic alkalosis and intravascular volume contraction to activate Oxgr1 in PP-IC, which in turn activates the multitransport protein network to drive salt reabsorption and bicarbonate secretion by these cells.
    Summary: Recent studies identify a novel salt transport pathway in intercalated cells that is activated by an intrarenal paracrine system, α-ketoglutartate/Oxgr1. Activation of the paracrine system and transport pathway, particularly during alkalosis and volume contraction, mitigates deleterious salt wasting while restoring acid-base balance.
    Language English
    Publishing date 2017-09
    Publishing country England
    Document type Journal Article
    ZDB-ID 1151092-4
    ISSN 1473-6543 ; 1535-3842 ; 1062-4813 ; 1062-4821
    ISSN (online) 1473-6543 ; 1535-3842
    ISSN 1062-4813 ; 1062-4821
    DOI 10.1097/MNH.0000000000000353
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Does the early aldosterone-induced SGK1 play a role in early Kaliuresis?

    Al-Qusairi, Lama / Basquin, Denis / Stifanelli, Matteo / Welling, Paul A / Staub, Olivier

    Physiological reports

    2022  Volume 10, Issue 4, Page(s) e15188

    Abstract: ... Urinary ... ...

    Abstract Urinary K
    MeSH term(s) Aldosterone ; Animals ; Epithelial Sodium Channels/genetics ; Mice ; Nedd4 Ubiquitin Protein Ligases/genetics ; Potassium/metabolism ; Sodium/metabolism ; Sodium Chloride, Dietary/metabolism ; Solute Carrier Family 12, Member 3/genetics
    Chemical Substances Epithelial Sodium Channels ; Sodium Chloride, Dietary ; Solute Carrier Family 12, Member 3 ; Aldosterone (4964P6T9RB) ; Sodium (9NEZ333N27) ; Nedd4 Ubiquitin Protein Ligases (EC 2.3.2.26) ; Potassium (RWP5GA015D)
    Language English
    Publishing date 2022-02-10
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2724325-4
    ISSN 2051-817X ; 2051-817X
    ISSN (online) 2051-817X
    ISSN 2051-817X
    DOI 10.14814/phy2.15188
    Database MEDical Literature Analysis and Retrieval System OnLINE

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