The Na <sup>+</sup> /K <sup>+</sup> ‐ATPase β1 Subunit is a Kidney ADP‐Ribosyl Cyclase

ADP-ribosyl cyclase (ARC) produces a Ca<sup>2+</sup>-mobilizing second messenger, cyclic ADP-ribose (cADPR), from NAD. In this study, we purified an ARC from rat kidney, which was identified as the β1 subunit of Na, K-ATPase (Atp1b1). Recombinant Atp1b1 exhibited ARC activity and generated cADPR. Knockdown of Atp1b1 in mouse mesangial cells (MES-13) inhibited angiotensin II (AngII)-induced cADPR synthesis and the subsequent long-lasting Ca<sup>2+</sup> signals. These findings demonstrate that Atp1b1 is coupled with the AngII receptor and is activated to produce cADPR, thereby mediating Ca<sup>2+</sup> signaling in the kidney.

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Publication Details

Journal
The FASEB Journal
Published
2025-10-14
DOI
https://doi.org/10.1096/fj.202502065rr
Primary Topic
Calcium signaling and nucleotide metabolism
Type
article
Field-Weighted Citation Impact
0.00

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article

The Na + /K + ‐ATPase β1 Subunit is a Kidney ADP‐Ribosyl Cyclase

Tae‐Sik Nam, Uh‐Hyun Kim, Seong‐Kyu Choe
The FASEB Journal
Calcium signaling and nucleotide metabolism
article

The Na + /K + ‐ATPase β1 Subunit is a Kidney ADP‐Ribosyl Cyclase

Tae‐Sik Nam, Uh‐Hyun Kim, Seong‐Kyu Choe
article en

Abstract

ADP-ribosyl cyclase (ARC) produces a Ca<sup>2+</sup>-mobilizing second messenger, cyclic ADP-ribose (cADPR), from NAD. In this study, we purified an ARC from rat kidney, which was identified as the β1 subunit of Na, K-ATPase (Atp1b1). Recombinant Atp1b1 exhibited ARC activity and generated cADPR. Knockdown of Atp1b1 in mouse mesangial cells (MES-13) inhibited angiotensin II (AngII)-induced cADPR synthesis and the subsequent long-lasting Ca<sup>2+</sup> signals. These findings demonstrate that Atp1b1 is coupled with the AngII receptor and is activated to produce cADPR, thereby mediating Ca<sup>2+</sup> signaling in the kidney.

The FASEB JournalVol. 39(20)
Wonkwang University (KR)
National Research Foundation, National Research Foundation of Korea
Openalex Percentile: Top 71%
Calcium signaling and nucleotide metabolism
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