Inhye Park
DPhil
BHF CRE Intermediate Transition Research Fellow
I undertook my DPhil project in the laboratory of Prof. Claudia Monaco at the University of Oxford to investigate how a C-type lectin receptor CLEC4A2 directs macrophages towards a protective function in atherosclerosis. In 2021, I was awarded a Novo Nordisk Fellowship to identify key transcription factors that define tissue identity of resident vascular macrophages using in vitro and in vivo validation. The project aimed to identify target genes that were conserved in resident macrophages in human and mouse vascular tissues. Target validation was performed using a platform that combines vascular co-culture and CRISPR screens and functional studies in murine models of atherosclerosis. To pursue my independent research, I applied for a BHF CRE Transition Fellowship to explore the role of a novel subset of vascular macrophages identified in my previous studies in acute and chronic heart failure models. This work will be supported by two leading experts in this field, Prof. Paul Riley (IDRM) in cardiovascular regenerative medicine and Prof. Claudia Monaco (Kennedy, NDORMS) in cardiovascular inflammation. Through this fellowship, I aim to build on my own research linking immunology and metabolism in macrophages in CVD and identifying therapeutic targets for translational application in the clinic.
Recent publications
Identification of a non-canonical chemokine-receptor pathway suppressing regulatory T cells to drive atherosclerosis.
Journal article
Döring Y. et al, (2024), Nat Cardiovasc Res, 3, 221 - 242
Interferon regulatory factor-5-dependent CD11c+ macrophages contribute to the formation of rupture-prone atherosclerotic plaques.
Journal article
Edsfeldt A. et al, (2022), Eur Heart J, 43, 1864 - 1877
blood atlas of COVID-19 defines hallmarks of disease severity and specificity.
Journal article
COvid-19 Multi-omics Blood ATlas (COMBAT) Consortium. Electronic address: julian.knight@well.ox.ac.uk . and COvid-19 Multi-omics Blood ATlas (COMBAT) Consortium ., (2022), Cell, 185, 916 - 938.e58
Interferon regulatory factor-5-dependent CD11c+ macrophages contribute to the formation of rupture-prone atherosclerotic plaques.
Journal article
Edsfeldt A. et al, (2022), Eur Heart J
C-type lectin receptor CLEC4A2 promotes tissue adaptation of macrophages and protects against atherosclerosis.
Journal article
Park I. et al, (2022), Nat Commun, 13

