Literature DB >> 26534937

Pappa2 is linked to salt-sensitive hypertension in Dahl S rats.

Allen W Cowley1, Chun Yang2, Vikash Kumar2, Jozef Lazar3, Howard Jacob4, Aron M Geurts5, Pengyuan Liu6, Alex Dayton2, Theresa Kurth2, Mingyu Liang2.   

Abstract

A 1.37 Mbp region of chromosome 13 previously identified by exclusion mapping was consistently associated with a reduction of salt-induced hypertension in the Dahl salt-sensitive (SS) rat. This region contained five genes that were introgressed from the salt-insensitive Brown Norway (BN) rat. The goal of the present study was to further narrow that region to identify the gene(s) most likely to protect from salt-induced hypertension. The studies yielded a subcongenic SS rat strain containing a 0.71 Mbp insert from BN (26-P strain) in which salt-induced hypertension was reduced by 24 mmHg. The region contained two protein-coding genes (Astn1 and Pappa2) and a microRNA (miR-488). Pappa2 mRNA in the renal cortex of the protected 26-P was 6- to 10-fold greater than in SS fed a 0.4% NaCl diet but was reduced to levels observed in SS when fed 8.0% NaCl diet for 7 days. Compared with brain nuclei (NTS, RVLM, CVLM) and the adrenal gland, Pappa2 in the renal cortex was the only gene found to be differentially expressed between SS and 26-P and that responded to changes of salt diet. Immunohistochemistry studies found Pappa2 localized in the cytosol of the epithelial cells of the cortical thick ascending limbs. In more distal segments of the renal tubules, it was observed within tubular lumens and most notably bound to the apical membranes of the intercalated cells of collecting ducts. We conclude that we have identified a variant form of Pappa2 that can protect against salt-induced hypertension in the Dahl S rat.
Copyright © 2016 the American Physiological Society.

Entities:  

Keywords:  Astn1; Dahl S rats; ENaC; Na excretion; Pappa2; congenic; genetics; intercalated cells; kidney; miR-488; renal collecting ducts; thick ascending limbs

Mesh:

Substances:

Year:  2015        PMID: 26534937      PMCID: PMC4757026          DOI: 10.1152/physiolgenomics.00097.2015

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


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