Transport, cilia, and PKD: must we in (cyst) on interrelationships? Focus on “Increased Na+/H+ exchanger activity on the apical surface of a cilium-deficient cortical collecting duct principal cell model of polycystic kidney disease”

Avner, Ellis D.; McDonough, Alicia A.; Sweeney, William E.

doi:10.1152/ajpcell.00070.2012

Cited by 6 publications

(3 citation statements)

References 13 publications

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“…NHE1 is mislocalized to the apical membrane in PKD cell models where it absorbs Na + ions, in exchange for H + (Avner et al . ; Olteanu et al . ).…”

Section: Discussionmentioning

confidence: 99%

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NHA2 promotes cyst development in an in vitro model of polycystic kidney disease

Prasad

Dang

Kondapalli

et al. 2018

The Journal of Physiology

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Key points Significant and selective up‐regulation of the Na+/H+ exchanger NHA2 (SLC9B2) was observed in cysts of patients with autosomal dominant polycystic kidney disease. Using the MDCK cell model of cystogenesis, it was found that NHA2 increases cyst size. Silencing or pharmacological inhibition of NHA2 inhibits cyst formation in vitro. Polycystin‐1 represses NHA2 expression via Ca2+/NFAT signalling whereas the dominant negative membrane‐anchored C‐terminal fragment (PC1‐MAT) increased NHA2 levels. Drugs (caffeine, theophylline) and hormones (vasopressin, aldosterone) known to exacerbate cysts elicit NHA2 expression. Taken together, the findings reveal NHA2 as a potential new player in salt and water homeostasis in the kidney and in the pathogenesis of polycystic kidney disease. Abstract Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in PKD1 and PKD2 encoding polycystin‐1 (PC1) and polycystin‐2 (PC2), respectively. The molecular pathways linking polycystins to cyst development in ADPKD are still unclear. Intracystic fluid secretion via ion transporters and channels plays a crucial role in cyst expansion in ADPKD. Unexpectedly, we observed significant and selective up‐regulation of NHA2, a member of the SLC9B family of Na+/H+ exchangers, that correlated with cyst size and disease severity in ADPKD patients. Using three‐dimensional cultures of MDCK cells to model cystogenesis in vitro, we showed that ectopic expression of NHA2 is causal to increased cyst size. Induction of PC1 in MDCK cells inhibited NHA2 expression with concordant inhibition of Ca2+ influx through store‐dependent and ‐independent pathways, whereas reciprocal activation of Ca2+ influx by the dominant negative membrane‐anchored C‐terminal tail fragment of PC1 elevated NHA2. We showed that NHA2 is a target of Ca2+/NFAT signalling and is transcriptionally induced by methylxanthine drugs such as caffeine and theophylline, which are contraindicated in ADPKD patients. Finally, we observed robust induction of NHA2 by vasopressin, which is physiologically consistent with increased levels of circulating vasopressin and up‐regulation of vasopressin V2 receptors in ADPKD. Our findings have mechanistic implications on the emerging use of vasopressin V2 receptor antagonists such as tolvaptan as safe and effective therapy for polycystic kidney disease and reveal a potential new regulator of transepithelial salt and water transport in the kidney.

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“…NHE1 is mislocalized to the apical membrane in PKD cell models where it absorbs Na + ions, in exchange for H + (Avner et al . ; Olteanu et al . ).…”

Section: Discussionmentioning

confidence: 99%

“…In this context, increased plasma membrane Na + /H + exchange (NHE) activity has been reported in cilium‐deficient collecting duct cells from the Oak Ridge mouse model of polycystic kidney disease (Avner et al . ; Olteanu et al . ).…”

Section: Introductionmentioning

confidence: 99%

NHA2 promotes cyst development in an in vitro model of polycystic kidney disease

Prasad

Dang

Kondapalli

et al. 2018

The Journal of Physiology

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“…In this context, increased plasma membrane Na + /H + exchange (NHE) activity has been reported in cilium-deficient collecting duct cells from the Oak Ridge mouse model of polycystic kidney disease (8,9). Apical mislocalization of NHE1 in these cells leads to hyperabsorption of Na + and epidermal growth factor-induced cell proliferation (8,10).…”

Section: Introductionmentioning

confidence: 99%

NHA2 promotes cyst development in an in vitro model of polycystic kidney disease

Prasad

Dang

Kondapalli

et al. 2018

Preprint

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Key pointsr Significant and selective up-regulation of the Na + /H + exchanger NHA2 (SLC9B2) was observed in cysts of patients with autosomal dominant polycystic kidney disease.r Using the MDCK cell model of cystogenesis, it was found that NHA2 increases cyst size.Silencing or pharmacological inhibition of NHA2 inhibits cyst formation in vitro.r Polycystin-1 represses NHA2 expression via Ca 2+ /NFAT signalling whereas the dominant negative membrane-anchored C-terminal fragment (PC1-MAT) increased NHA2 levels.r Drugs (caffeine, theophylline) and hormones (vasopressin, aldosterone) known to exacerbate cysts elicit NHA2 expression.r Taken together, the findings reveal NHA2 as a potential new player in salt and water homeostasis in the kidney and in the pathogenesis of polycystic kidney disease.Abstract Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in PKD1 and PKD2 encoding polycystin-1 (PC1) and polycystin-2 (PC2), respectively. The molecular pathways linking polycystins to cyst development in ADPKD are still unclear. Intracystic fluid secretion via ion transporters and channels plays a crucial role in cyst expansion in ADPKD. Unexpectedly, we observed significant and selective up-regulation of NHA2, a member of the SLC9B family of Na + /H + exchangers, that correlated with cyst size and disease severity in ADPKD patients. Using three-dimensional cultures of MDCK cells to model cystogenesis in vitro, we showed that ectopic expression of NHA2 is causal to increased cyst size. Induction of PC1 in MDCK cells inhibited NHA2 expression with concordant inhibition of Ca 2+ influx through store-dependent and -independent pathways, whereas reciprocal activation of Ca 2+ influx by the dominant negative membrane-anchored C-terminal tail fragment of PC1 elevated NHA2. We showed that NHA2 is a target of Ca 2+ /NFAT signalling and is transcriptionally induced by

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What Is Your Family History? The Molecular Genetics of Inherited Kidney Diseases

Rayner

Thomas

Milford

2020

Understanding Kidney Diseases

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Transport, cilia, and PKD: must we in (cyst) on interrelationships? Focus on “Increased Na⁺/H⁺ exchanger activity on the apical surface of a cilium-deficient cortical collecting duct principal cell model of polycystic kidney disease”

Cited by 6 publications

References 13 publications

NHA2 promotes cyst development in an in vitro model of polycystic kidney disease

NHA2 promotes cyst development in an in vitro model of polycystic kidney disease

NHA2 promotes cyst development in an in vitro model of polycystic kidney disease

What Is Your Family History? The Molecular Genetics of Inherited Kidney Diseases

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