Constitutive expression of inducible nitric oxide synthase in healthy rat urothelium?Show others and affiliations
2021 (English)In: Scandinavian journal of urology, ISSN 2168-1805, E-ISSN 2168-1813, Vol. 55, no 6, p. 493-497Article in journal (Refereed) Published
Abstract [en]
BACKGROUND: Contrasting findings have been reported regarding a possible constitutive expression of inducible nitric oxide synthase (iNOS) in a normal mammalian bladder. The current study was designed to further investigate such putative iNOS expression.
MATERIALS AND METHODS: The experiments were conducted with paraffin-embedded archival material from the urinary bladder of 6 normal, male Sprague-Dawley rats. In addition, two normal female mice (C57BL/6) were sacrificed and the urinary bladders were harvested. The occurrence of iNOS mRNA was examined by the RNAScope in situ hybridization method. Protein expression of iNOS and 3-nitrotyrosine (the latter used as an indicator of oxidative stress) was investigated by immunohistochemistry.
RESULTS: No expression of iNOS mRNA was observed in the bladder tissue. iNOS protein and 3-nitrotyrosine were strongly expressed in the urothelium. iNOS was also expressed perinuclearly in the detrusor.
CONCLUSIONS: Although the RNAScope methodology could not demonstrate mRNA for iNOS in the normal urinary bladder, the results by immunohistochemistry strongly suggest the occurrence of iNOS in particular, in the urothelium. Positive reactivity for 3-nitrotyrosine may indicate ongoing oxidative stress of the urothelium. The finding of perinuclear iNOS immunoreactivity could suggest an intracrine signaling function by iNOS to the nucleus.
Place, publisher, year, edition, pages
Taylor & Francis, 2021. Vol. 55, no 6, p. 493-497
Keywords [en]
Immunohistochemistry, in situ hybridization, inducible, mRNA, nitric oxide synthase, nuclear, rat, urinary bladder, urothelium
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:oru:diva-95198DOI: 10.1080/21681805.2021.1948097ISI: 000710400200001PubMedID: 34689710Scopus ID: 2-s2.0-85118106793OAI: oai:DiVA.org:oru-95198DiVA, id: diva2:1627010
Note
Funding agencies:
Anna-Lisa and Bror Björnsson's Research Foundation
Martha and Gustaf Ågren's Research Foundation
Örebro University
Swedish government
2022-01-122022-01-122022-01-12Bibliographically approved