Defects in V-ATPase-dependent acidification in the kidney collecting duct results in distal tubular acidosis and nephrolithiasis. This MERIT award focuses on the role of intercalated cells (IC) in modulating proton secretion via the V-ATPase. Since the start of this award in 2008, we have published 20 original papers and 4 review articles on V- ATPase function and protein trafficking. Our work, summarized in the progress report, includes identifying signal transduction and trafficking pathways regulating proton- secretion by IC;identifying new V-ATPase interacting proteins;revealing many new splice variants of V-ATPase subunits that may have cell specific roles;performing an exhaustive proteomic analysis of 10;characterizing accessory proteins involved in trafficking pathways in different kidney tubules;generating new knockout and transgenic mice that open new avenues for understanding IC development and V-ATPase function; identifying multiple phosphorylation sites on V-ATPase subunits by mass spectrometry. Importantly, we have developed techniques to maintain differentiated 10 in vitro for several days. This now allows us unprecedented access to their proteome, RNA expression, and their acidification function in direct response to physiological/hormonal stimuli. In the extension period, we will: 1) Exterid our ongoing studies to identify the sensing and signal transduction cascade that leads to modulation of acid/base transport by 10 in the kidneys of normal and V-ATPase subunit-depJeted mice, and in our isolated EGFP-IC in vitro. We will use V-ATPase-Cre mice to selectively delete critical proteins including the soluble adenylyl cyclase (sAO), cytoskeletal proteins and accessory trafficking proteins from ICs. In vitro real time and in vivo intravital microscopy as well as functional measurements of proton secretion will be applied to follow 10 responses to stimuli. 2) We will dissect protein interactions and phosphorylation events that regulate V-ATPase trafficking and function a) by continuing to characterize cytoskeletal protein interactions (including FRET and Biacore assays) and b) by identifying phosphorylation events necessary for V-ATPase activation using expression of phosphomutant subunits in our cell culture systems. We will continue producing anti-phospho-V-ATPase antibodies. 3) We will characterize the expression, distribution and function of newly- identified V-ATPase a4 subunit splice variants that could explain differential membrane targeting of V-ATPase in 10 and other cells. In summary, our proposed studies are focused on the application-of new tools that will ultimately allow us to therapeutically modify renal acidification process by understanding acid/base sensing and V-ATPase trafficking mechanisms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37DK042956-22
Application #
8655149
Study Section
Special Emphasis Panel (NSS)
Program Officer
Mullins, Christopher V
Project Start
1991-08-01
Project End
2018-03-31
Budget Start
2014-04-01
Budget End
2015-03-31
Support Year
22
Fiscal Year
2014
Total Cost
$411,247
Indirect Cost
$167,397
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Battistone, Maria A; Nair, Anil V; Barton, Claire R et al. (2018) Extracellular Adenosine Stimulates Vacuolar ATPase-Dependent Proton Secretion in Medullary Intercalated Cells. J Am Soc Nephrol 29:545-556
Merkulova, Maria; P?unescu, Teodor G; Nair, Anil V et al. (2018) Targeted deletion of the Ncoa7 gene results in incomplete distal renal tubular acidosis in mice. Am J Physiol Renal Physiol 315:F173-F185
Christensen, Henriette L; P?unescu, Teodor G; Matchkov, Vladimir et al. (2017) The V-ATPase is expressed in the choroid plexus and mediates cAMP-induced intracellular pH alterations. Physiol Rep 5:
Chen, Lihe; Lee, Jae Wook; Chou, Chung-Lin et al. (2017) Transcriptomes of major renal collecting duct cell types in mouse identified by single-cell RNA-seq. Proc Natl Acad Sci U S A 114:E9989-E9998
Chen, Ying-Chu; Backus, Keriann M; Merkulova, Maria et al. (2017) Covalent Modulators of the Vacuolar ATPase. J Am Chem Soc 139:639-642
Mumtaz, Rizwan; Trepiccione, Francesco; Hennings, J Christopher et al. (2017) Intercalated Cell Depletion and Vacuolar H+-ATPase Mistargeting in an Ae1 R607H Knockin Model. J Am Soc Nephrol 28:1507-1520
Cotter, Kristina; Liberman, Rachel; Sun-Wada, GeHong et al. (2016) The a3 isoform of subunit a of the vacuolar ATPase localizes to the plasma membrane of invasive breast tumor cells and is overexpressed in human breast cancer. Oncotarget 7:46142-46157
Trepiccione, Francesco; Gerber, Simon D; Grahammer, Florian et al. (2016) Renal Atp6ap2/(Pro)renin Receptor Is Required for Normal Vacuolar H+-ATPase Function but Not for the Renin-Angiotensin System. J Am Soc Nephrol 27:3320-3330
Inoue, Yoshitaka; Yu, Yong-Ming; Kurihara, Tomohiro et al. (2016) Kidney and Liver Injuries After Major Burns in Rats Are Prevented by Resolvin D2. Crit Care Med 44:e241-52
Azroyan, Anie; Cortez-Retamozo, Virna; Bouley, Richard et al. (2015) Renal intercalated cells sense and mediate inflammation via the P2Y14 receptor. PLoS One 10:e0121419

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