Matthew R Alexander1, Allison E Norlander2, Fernando Elijovich3, Ravi V Atreya4, Amadou Gaye5, Juan S Gnecco6, Cheryl L Laffer3, Cristi L Galindo1, Meena S Madhur1,2,3. 1. Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, USA. 2. Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA. 3. Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA. 4. Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA. 5. Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, National Human Genome Research Institute, Bethesda, MD, USA. 6. Department of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN, USA.
Abstract
BACKGROUND AND PURPOSE: Monocytes play a critical role in hypertension. The purpose of our study was to use an unbiased approach to determine whether hypertensive individuals on conventional therapy exhibit an altered monocyte gene expression profile and to perform validation studies of selected genes to identify novel therapeutic targets for hypertension. EXPERIMENTAL APPROACH: Next generation RNA sequencing identified differentially expressed genes in a small discovery cohort of normotensive and hypertensive individuals. Several of these genes were further investigated for association with hypertension in multiple validation cohorts using qRT-PCR, regression analysis, phenome-wide association study and case-control analysis of a missense polymorphism. KEY RESULTS: We identified 60 genes that were significantly differentially expressed in hypertensive monocytes, many of which are related to IL-1β. Uni- and multivariate regression analyses of the expression of these genes with mean arterial pressure (MAP) revealed four genes that significantly correlated with MAP in normotensive and/or hypertensive individuals. Of these, lactoferrin (LTF), peptidoglycan recognition protein 1 and IL-18 receptor accessory protein (IL18RAP) remained significantly elevated in peripheral monocytes of hypertensive individuals in a separate validation cohort. Interestingly, IL18RAP expression associated with MAP in a cohort of African Americans. Furthermore, homozygosity for a missense single nucleotide polymorphism in LTF that decreases antimicrobial function and increases protein levels (rs1126478) was over-represented in patients with hypertension relative to controls (odds ratio 1.16). CONCLUSIONS AND IMPLICATIONS: These data demonstrate that monocytes exhibit enhanced pro-inflammatory gene expression in hypertensive individuals and identify IL18RAP and LTF as potential novel mediators of human hypertension. LINKED ARTICLES: This article is part of a themed section on Immune Targets in Hypertension. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.12/issuetoc.
BACKGROUND AND PURPOSE: Monocytes play a critical role in hypertension. The purpose of our study was to use an unbiased approach to determine whether hypertensive individuals on conventional therapy exhibit an altered monocyte gene expression profile and to perform validation studies of selected genes to identify novel therapeutic targets for hypertension. EXPERIMENTAL APPROACH: Next generation RNA sequencing identified differentially expressed genes in a small discovery cohort of normotensive and hypertensive individuals. Several of these genes were further investigated for association with hypertension in multiple validation cohorts using qRT-PCR, regression analysis, phenome-wide association study and case-control analysis of a missense polymorphism. KEY RESULTS: We identified 60 genes that were significantly differentially expressed in hypertensive monocytes, many of which are related to IL-1β. Uni- and multivariate regression analyses of the expression of these genes with mean arterial pressure (MAP) revealed four genes that significantly correlated with MAP in normotensive and/or hypertensive individuals. Of these, lactoferrin (LTF), peptidoglycan recognition protein 1 and IL-18 receptor accessory protein (IL18RAP) remained significantly elevated in peripheral monocytes of hypertensive individuals in a separate validation cohort. Interestingly, IL18RAP expression associated with MAP in a cohort of African Americans. Furthermore, homozygosity for a missense single nucleotide polymorphism in LTF that decreases antimicrobial function and increases protein levels (rs1126478) was over-represented in patients with hypertension relative to controls (odds ratio 1.16). CONCLUSIONS AND IMPLICATIONS: These data demonstrate that monocytes exhibit enhanced pro-inflammatory gene expression in hypertensive individuals and identify IL18RAP and LTF as potential novel mediators of humanhypertension. LINKED ARTICLES: This article is part of a themed section on Immune Targets in Hypertension. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.12/issuetoc.
Authors: George Davey Smith; Debbie A Lawlor; Roger Harbord; Nic Timpson; Ann Rumley; Gordon D O Lowe; Ian N M Day; Shah Ebrahim Journal: Arterioscler Thromb Vasc Biol Date: 2005-02-24 Impact factor: 8.311
Authors: Y Dörffel; C Lätsch; B Stuhlmüller; S Schreiber; S Scholze; G R Burmester; J Scholze Journal: Hypertension Date: 1999-07 Impact factor: 10.190
Authors: Rebecca P Gelber; J Michael Gaziano; JoAnn E Manson; Julie E Buring; Howard D Sesso Journal: Am J Hypertens Date: 2007-04 Impact factor: 2.689
Authors: José Maria Moreno-Navarrete; Francisco José Ortega; Judit Bassols; Antoni Castro; Wifredo Ricart; José Manuel Fernández-Real Journal: Clin Chem Date: 2007-12-21 Impact factor: 8.327
Authors: Asif Nashiry; Shauli Sarmin Sumi; Salequl Islam; Julian M W Quinn; Mohammad Ali Moni Journal: Brief Bioinform Date: 2021-03-22 Impact factor: 11.622
Authors: Melis Sahinoz; Fernando Elijovich; Lale A Ertuglu; Jeanne Ishimwe; Ashley Pitzer; Mohammad Saleem; Naome Mwesigwa; Thomas R Kleyman; Cheryl L Laffer; Annet Kirabo Journal: Antioxid Redox Signal Date: 2021-12-20 Impact factor: 8.401
Authors: Meena S Madhur; Fernando Elijovich; Matthew R Alexander; Ashley Pitzer; Jeanne Ishimwe; Justin P Van Beusecum; David M Patrick; Charles D Smart; Thomas R Kleyman; Justin Kingery; Robert N Peck; Cheryl L Laffer; Annet Kirabo Journal: Circ Res Date: 2021-04-01 Impact factor: 17.367