Nephron prorenin receptor deficiency alters renal medullary endothelin-1 and endothelin receptor expression
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
Grantová podpora
P01 HL136267
NHLBI NIH HHS - United States
PubMed
29947533
PubMed Central
PMC6355149
DOI
10.33549/physiolres.933809
PII: 933809
Knihovny.cz E-zdroje
- MeSH
- dřeň ledvin metabolismus MeSH
- endotelin-1 biosyntéza genetika MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- myši MeSH
- nefrony metabolismus MeSH
- receptor endotelinu A biosyntéza genetika MeSH
- receptor endotelinu B biosyntéza genetika MeSH
- receptor proreninu MeSH
- receptory buněčného povrchu nedostatek MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- endotelin-1 MeSH
- receptor endotelinu A MeSH
- receptor endotelinu B MeSH
- receptor proreninu MeSH
- receptory buněčného povrchu MeSH
The endothelin (ET) and prorenin/renin/prorenin receptor (PRR) systems have opposing physiological effects on collecting duct (CD) salt and water reabsorption. It is unknown if the CD ET and renin/PRR systems interact, hence we examined the effects of deleting CD renin or nephron PRR on CD ET system components. PRR knockout (KO) mice were polyuric and had markedly increased urinary ET-1 and inner medullary CD (IMCD) ET-1 mRNA. PRR KO mice had greatly increased IMCD ETA receptor mRNA and protein, while ETB mRNA and protein were decreased. Water loaded wild-type mice with similar polyuria as PRR KO mice had modestly increased urinary ET-1 excretion and inner medullary ET-1 mRNA, while inner medullary ETA and ETB mRNA or protein expression were unaffected. In contrast to PRR KO, CD prorenin/renin KO did not alter ET system components. Taken together, these results suggest that the nephron PRR is involved in regulating CD ET system expression, but this effect may be independent of CD-derived renin.
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