Gene expression profiles during tissue remodeling following bladder outlet obstruction

Abstract Bladder outlet obstruction (BOO) often results in lower urinary tract symptoms (LUTSs) and negatively affects quality of life. Here, we evaluated gene expression patterns in the urinary bladder during tissue remodeling due to BOO. We divided BOO model rats into two groups according to the d...

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Autores principales: Saya Ito, Takeshi Nomura, Takashi Ueda, Shogo Inui, Yukako Morioka, Hisashi Honjo, Ayako Fukui, Atsuko Fujihara, Fumiya Hongo, Osamu Ukimura
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/9d1aac88f93c4a0494190c13d14503bf
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spelling oai:doaj.org-article:9d1aac88f93c4a0494190c13d14503bf2021-12-02T16:07:04ZGene expression profiles during tissue remodeling following bladder outlet obstruction10.1038/s41598-021-92756-12045-2322https://doaj.org/article/9d1aac88f93c4a0494190c13d14503bf2021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-92756-1https://doaj.org/toc/2045-2322Abstract Bladder outlet obstruction (BOO) often results in lower urinary tract symptoms (LUTSs) and negatively affects quality of life. Here, we evaluated gene expression patterns in the urinary bladder during tissue remodeling due to BOO. We divided BOO model rats into two groups according to the degree of hypertrophy of smooth muscle in the bladder. The strong muscular hypertrophy group, which exhibited markedly increased bladder smooth muscle proportion and HIF1α mRNA levels compared with the control group, was considered a model for the termination of hypertrophy, whereas the mild muscular hypertrophy group was considered a model of the initiation of hypertrophy. Some genes related to urinary function showed different expression patterns between the two groups. Furthermore, we found that several genes, including D-box binding PAR bZIP transcription factor (DBP), were upregulated only in the mild muscular hypertrophy group. DBP expression levels were increased in bladder smooth muscle cells in response to hypoxic stress. DBP associated with enhancer and promoter regions of NOS3 gene locus and upregulated NOS3 gene expression under hypoxic conditions. These findings suggested that the regulatory systems of gene expression were altered during tissue remodeling following BOO. Furthermore, circadian clock components might be involved in control of urinary function via transcriptional gene regulation in response to hypoxic stimuli.Saya ItoTakeshi NomuraTakashi UedaShogo InuiYukako MoriokaHisashi HonjoAyako FukuiAtsuko FujiharaFumiya HongoOsamu UkimuraNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Saya Ito
Takeshi Nomura
Takashi Ueda
Shogo Inui
Yukako Morioka
Hisashi Honjo
Ayako Fukui
Atsuko Fujihara
Fumiya Hongo
Osamu Ukimura
Gene expression profiles during tissue remodeling following bladder outlet obstruction
description Abstract Bladder outlet obstruction (BOO) often results in lower urinary tract symptoms (LUTSs) and negatively affects quality of life. Here, we evaluated gene expression patterns in the urinary bladder during tissue remodeling due to BOO. We divided BOO model rats into two groups according to the degree of hypertrophy of smooth muscle in the bladder. The strong muscular hypertrophy group, which exhibited markedly increased bladder smooth muscle proportion and HIF1α mRNA levels compared with the control group, was considered a model for the termination of hypertrophy, whereas the mild muscular hypertrophy group was considered a model of the initiation of hypertrophy. Some genes related to urinary function showed different expression patterns between the two groups. Furthermore, we found that several genes, including D-box binding PAR bZIP transcription factor (DBP), were upregulated only in the mild muscular hypertrophy group. DBP expression levels were increased in bladder smooth muscle cells in response to hypoxic stress. DBP associated with enhancer and promoter regions of NOS3 gene locus and upregulated NOS3 gene expression under hypoxic conditions. These findings suggested that the regulatory systems of gene expression were altered during tissue remodeling following BOO. Furthermore, circadian clock components might be involved in control of urinary function via transcriptional gene regulation in response to hypoxic stimuli.
format article
author Saya Ito
Takeshi Nomura
Takashi Ueda
Shogo Inui
Yukako Morioka
Hisashi Honjo
Ayako Fukui
Atsuko Fujihara
Fumiya Hongo
Osamu Ukimura
author_facet Saya Ito
Takeshi Nomura
Takashi Ueda
Shogo Inui
Yukako Morioka
Hisashi Honjo
Ayako Fukui
Atsuko Fujihara
Fumiya Hongo
Osamu Ukimura
author_sort Saya Ito
title Gene expression profiles during tissue remodeling following bladder outlet obstruction
title_short Gene expression profiles during tissue remodeling following bladder outlet obstruction
title_full Gene expression profiles during tissue remodeling following bladder outlet obstruction
title_fullStr Gene expression profiles during tissue remodeling following bladder outlet obstruction
title_full_unstemmed Gene expression profiles during tissue remodeling following bladder outlet obstruction
title_sort gene expression profiles during tissue remodeling following bladder outlet obstruction
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/9d1aac88f93c4a0494190c13d14503bf
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