Identification of a gene network driving the attenuated response to lipopolysaccharide of monocytes from hypertensive coronary artery disease patients

Introduction: The impact of cardiovascular disease (CVD) risk factors, encompassing various biological determinants and unhealthy lifestyles, on the functional dynamics of circulating monocytes - a pivotal cell type in CVD pathophysiology remains elusive. In this study, we aimed to elucidate the inf...

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Hauptverfasser: Lu, Chang (VerfasserIn) , Donners, Marjo M. P. C. (VerfasserIn) , de Baaij, Julius B. J. (VerfasserIn) , Jin, Han (VerfasserIn) , Otten, Jeroen J. T. (VerfasserIn) , Manca, Marco (VerfasserIn) , van Zonneveld, Anton Jan (VerfasserIn) , Jukema, J. Wouter (VerfasserIn) , Kraaijeveld, Adriaan (VerfasserIn) , Kuiper, Johan (VerfasserIn) , Pasterkamp, Gerard (VerfasserIn) , Mees, Barend (VerfasserIn) , Sluimer, Judith C. (VerfasserIn) , Cavill, Rachel (VerfasserIn) , Karel, Joël M. H. (VerfasserIn) , Goossens, Pieter (VerfasserIn) , Biessen, Erik A. L. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 12 February 2024
In: Frontiers in immunology
Year: 2024, Jahrgang: 15, Pages: 1-13
ISSN:1664-3224
DOI:10.3389/fimmu.2024.1286382
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.3389/fimmu.2024.1286382
Verlag, kostenfrei, Volltext: https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1286382/full
Volltext
Verfasserangaben:Chang Lu, Marjo M.P.C. Donners, Julius B.J. de Baaij, Han Jin, Jeroen J.T. Otten, Marco Manca, Anton Jan van Zonneveld, J. Wouter Jukema, Adriaan Kraaijeveld, Johan Kuiper, Gerard Pasterkamp, Barend Mees, Judith C. Sluimer, Rachel Cavill, Joël M.H. Karel, Pieter Goossens and Erik A.L. Biessen

MARC

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245 1 0 |a Identification of a gene network driving the attenuated response to lipopolysaccharide of monocytes from hypertensive coronary artery disease patients  |c Chang Lu, Marjo M.P.C. Donners, Julius B.J. de Baaij, Han Jin, Jeroen J.T. Otten, Marco Manca, Anton Jan van Zonneveld, J. Wouter Jukema, Adriaan Kraaijeveld, Johan Kuiper, Gerard Pasterkamp, Barend Mees, Judith C. Sluimer, Rachel Cavill, Joël M.H. Karel, Pieter Goossens and Erik A.L. Biessen 
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520 |a Introduction: The impact of cardiovascular disease (CVD) risk factors, encompassing various biological determinants and unhealthy lifestyles, on the functional dynamics of circulating monocytes - a pivotal cell type in CVD pathophysiology remains elusive. In this study, we aimed to elucidate the influence of CVD risk factors on monocyte transcriptional responses to an infectious stimulus. Methods: We conducted a comparative analysis of monocyte gene expression profiles from the CTMM - CIRCULATING CELLS Cohort of coronary artery disease (CAD) patients, at baseline and after lipopolysaccharide (LPS) stimulation. Gene co-expression analysis was used to identify gene modules and their correlations with CVD risk factors, while pivotal transcription factors controlling the hub genes in these modules were identified by regulatory network analyses. The identified gene module was subjected to a drug repurposing screen, utilizing the LINCS L1000 database. Results: Monocyte responsiveness to LPS showed a highly significant, negative correlation with blood pressure levels (ρ< -0.4; P<10<sup>-80</sup>). We identified a ZNF12/ZBTB43-driven gene module closely linked to diastolic blood pressure, suggesting that monocyte responses to infectious stimuli, such as LPS, are attenuated in CAD patients with elevated diastolic blood pressure. This attenuation appears associated with a dampening of the LPS-induced suppression of oxidative phosphorylation. Finally, we identified the serine-threonine inhibitor MW-STK33-97 as a drug candidate capable of reversing this aberrant LPS response. Conclusions: Monocyte responses to infectious stimuli may be hampered in CAD patients with high diastolic blood pressure and this attenuated inflammatory response may be reversed by the serine-threonine inhibitor MW-STK33-97. Whether the identified gene module is a mere indicator of, or causal factor in diastolic blood pressure and the associated dampened LPS responses remains to be determined. 
650 4 |a circulating monocytes3 
650 4 |a coronary artery disease1 
650 4 |a gene regulatory network5 
650 4 |a hypertension2 
650 4 |a Inflammatory responses4 
700 1 |a Donners, Marjo M. P. C.  |e VerfasserIn  |4 aut 
700 1 |a de Baaij, Julius B. J.  |e VerfasserIn  |4 aut 
700 1 |a Jin, Han  |e VerfasserIn  |4 aut 
700 1 |a Otten, Jeroen J. T.  |e VerfasserIn  |4 aut 
700 1 |a Manca, Marco  |e VerfasserIn  |4 aut 
700 1 |a van Zonneveld, Anton Jan  |e VerfasserIn  |4 aut 
700 1 |a Jukema, J. Wouter  |e VerfasserIn  |4 aut 
700 1 |a Kraaijeveld, Adriaan  |e VerfasserIn  |4 aut 
700 1 |a Kuiper, Johan  |e VerfasserIn  |4 aut 
700 1 |a Pasterkamp, Gerard  |e VerfasserIn  |4 aut 
700 1 |a Mees, Barend  |e VerfasserIn  |4 aut 
700 1 |a Sluimer, Judith C.  |e VerfasserIn  |4 aut 
700 1 |a Cavill, Rachel  |e VerfasserIn  |4 aut 
700 1 |a Karel, Joël M. H.  |e VerfasserIn  |4 aut 
700 1 |a Goossens, Pieter  |e VerfasserIn  |4 aut 
700 1 |a Biessen, Erik A. L.  |e VerfasserIn  |4 aut 
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