Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.

Hypertension is a multifactorial disease with stage-specific gene expression changes occurring in multiple organs over time. The temporal sequence and the extent of gene regulatory network changes occurring across organs during the development of hypertension remain unresolved. In this study, female...

Full description

Saved in:
Bibliographic Details
Main Authors: Eden Hornung, Sirisha Achanta, Alison Moss, James S Schwaber, Rajanikanth Vadigepalli
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2024-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0313252
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846163583372623872
author Eden Hornung
Sirisha Achanta
Alison Moss
James S Schwaber
Rajanikanth Vadigepalli
author_facet Eden Hornung
Sirisha Achanta
Alison Moss
James S Schwaber
Rajanikanth Vadigepalli
author_sort Eden Hornung
collection DOAJ
description Hypertension is a multifactorial disease with stage-specific gene expression changes occurring in multiple organs over time. The temporal sequence and the extent of gene regulatory network changes occurring across organs during the development of hypertension remain unresolved. In this study, female spontaneously hypertensive (SHR) and normotensive Wistar Kyoto (WKY) rats were used to analyze expression patterns of 96 genes spanning inflammatory, metabolic, sympathetic, fibrotic, and renin-angiotensin (RAS) pathways in five organs, at five time points from the onset to established hypertension. We analyzed this multi-dimensional dataset containing ~15,000 data points and developed a data-driven dynamic network model that accounts for gene regulatory influences within and across visceral organs and multiple brainstem autonomic control regions. We integrated the data from female SHR and WKY with published multiorgan gene expression data from male SHR and WKY. In female SHR, catecholaminergic processes in the adrenal gland showed the earliest gene expression changes prior to inflammation-related gene expression changes in the kidney and liver. Hypertension pathogenesis in male SHR instead manifested early as catecholaminergic gene expression changes in brainstem and kidney, followed by an upregulation of inflammation-related genes in liver. RAS-related gene expression from the kidney-liver-lung axis was downregulated and intra-adrenal RAS was upregulated in female SHR, whereas the opposite pattern of gene regulation was observed in male SHR. We identified disease-specific and sex-specific differences in regulatory interactions within and across organs. The inferred multi-organ network model suggests a diminished influence of central autonomic neural circuits over multi-organ gene expression changes in female SHR. Our results point to the gene regulatory influence of the adrenal gland on spleen in female SHR, as compared to brainstem influence on kidney in male SHR. Our integrated molecular profiling and network modeling identified a stage-specific, sex-dependent, multi-organ cascade of gene regulation during the development of hypertension.
format Article
id doaj-art-de5dc4249c734a06b5b38cf725b3c5e2
institution Kabale University
issn 1932-6203
language English
publishDate 2024-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj-art-de5dc4249c734a06b5b38cf725b3c5e22024-11-19T05:31:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032024-01-011911e031325210.1371/journal.pone.0313252Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.Eden HornungSirisha AchantaAlison MossJames S SchwaberRajanikanth VadigepalliHypertension is a multifactorial disease with stage-specific gene expression changes occurring in multiple organs over time. The temporal sequence and the extent of gene regulatory network changes occurring across organs during the development of hypertension remain unresolved. In this study, female spontaneously hypertensive (SHR) and normotensive Wistar Kyoto (WKY) rats were used to analyze expression patterns of 96 genes spanning inflammatory, metabolic, sympathetic, fibrotic, and renin-angiotensin (RAS) pathways in five organs, at five time points from the onset to established hypertension. We analyzed this multi-dimensional dataset containing ~15,000 data points and developed a data-driven dynamic network model that accounts for gene regulatory influences within and across visceral organs and multiple brainstem autonomic control regions. We integrated the data from female SHR and WKY with published multiorgan gene expression data from male SHR and WKY. In female SHR, catecholaminergic processes in the adrenal gland showed the earliest gene expression changes prior to inflammation-related gene expression changes in the kidney and liver. Hypertension pathogenesis in male SHR instead manifested early as catecholaminergic gene expression changes in brainstem and kidney, followed by an upregulation of inflammation-related genes in liver. RAS-related gene expression from the kidney-liver-lung axis was downregulated and intra-adrenal RAS was upregulated in female SHR, whereas the opposite pattern of gene regulation was observed in male SHR. We identified disease-specific and sex-specific differences in regulatory interactions within and across organs. The inferred multi-organ network model suggests a diminished influence of central autonomic neural circuits over multi-organ gene expression changes in female SHR. Our results point to the gene regulatory influence of the adrenal gland on spleen in female SHR, as compared to brainstem influence on kidney in male SHR. Our integrated molecular profiling and network modeling identified a stage-specific, sex-dependent, multi-organ cascade of gene regulation during the development of hypertension.https://doi.org/10.1371/journal.pone.0313252
spellingShingle Eden Hornung
Sirisha Achanta
Alison Moss
James S Schwaber
Rajanikanth Vadigepalli
Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.
PLoS ONE
title Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.
title_full Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.
title_fullStr Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.
title_full_unstemmed Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.
title_short Multi-organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat.
title_sort multi organ gene expression analysis and network modeling reveal regulatory control cascades during the development of hypertension in female spontaneously hypertensive rat
url https://doi.org/10.1371/journal.pone.0313252
work_keys_str_mv AT edenhornung multiorgangeneexpressionanalysisandnetworkmodelingrevealregulatorycontrolcascadesduringthedevelopmentofhypertensioninfemalespontaneouslyhypertensiverat
AT sirishaachanta multiorgangeneexpressionanalysisandnetworkmodelingrevealregulatorycontrolcascadesduringthedevelopmentofhypertensioninfemalespontaneouslyhypertensiverat
AT alisonmoss multiorgangeneexpressionanalysisandnetworkmodelingrevealregulatorycontrolcascadesduringthedevelopmentofhypertensioninfemalespontaneouslyhypertensiverat
AT jamessschwaber multiorgangeneexpressionanalysisandnetworkmodelingrevealregulatorycontrolcascadesduringthedevelopmentofhypertensioninfemalespontaneouslyhypertensiverat
AT rajanikanthvadigepalli multiorgangeneexpressionanalysisandnetworkmodelingrevealregulatorycontrolcascadesduringthedevelopmentofhypertensioninfemalespontaneouslyhypertensiverat