Young-Mi Park
Ewha Womans University · Medicine
About the Lab
Professor Young-Mi Park's research lab focuses on the molecular mechanisms underlying atherosclerosis, with a central emphasis on the role of CD36 in macrophage dysfunction, foam cell formation, and immune cell trafficking. The lab investigates how oxidized low-density lipoprotein (oxLDL) signaling through CD36 contributes to chronic inflammation, impaired macrophage migration, and cellular polarization defects in atherosclerotic plaque development. Additionally, the lab explores the systemic links between oral infections—particularly *Porphyromonas gingivalis*—and gut microbiota dysbiosis in promoting cardiovascular disease. The research integrates in vitro cell biology, in vivo murine models, and multi-omics approaches such as 16S rRNA sequencing and lipid metabolism profiling.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15CD36 is a membrane glycoprotein that is present on various types of cells, including monocytes, macrophages, microvascular endothelial cells, adipocytes and platelets. Macrophage CD36 participates in atherosclerotic arterial lesion formation through its interaction with oxidized low-density lipoprotein (oxLDL), which triggers signaling cascades for inflammatory responses. CD36 functions in oxLDL uptake and foam cell formation, which is the initial critical stage of atherosclerosis. In addition,
The trapping of lipid-laden macrophages in the arterial intima is a critical but reversible step in atherogenesis. However, the mechanism by which this occurs is not clearly defined. Here, we tested in mice the hypothesis that CD36, a class B scavenger receptor expressed on macrophages, has a role in this process. Using both in vivo and in vitro migration assays, we found that oxidized LDL (oxLDL), but not native LDL, inhibited migration of WT mouse macrophages but not CD36-deficient cells. We f
CD36 is a membrane glycoprotein that is present on various types of cells, including monocytes, macrophages, microvascular endothelial cells, adipocytes and platelets. Macrophage CD36 participates in atherosclerotic arterial lesion formation through its interaction with oxidized low-density lipoprotein (oxLDL), which triggers signaling cascades for inflammatory responses. CD36 functions in oxLDL uptake and foam cell formation, which is the initial critical stage of atherosclerosis. In addition,
Cell polarization is essential for migration and the exploratory function of leukocytes. However, the mechanism by which cells maintain polarity or how cells revert to the immobilized state by gaining cellular symmetry is not clear. Previously we showed that interaction between oxidized low-density lipoprotein (oxLDL) and CD36 inhibits macrophage migration; in the current study we tested the hypothesis that oxLDL/CD36-induced inhibition of migration is the result of intracellular signals that re
AIM: The link between periodontitis and intestinal dysbiosis, two factors that contribute to atherosclerosis, has not been clearly defined. We investigated the integrative effects of oral infection with Porphyromonas gingivalis (PG), the major pathogen for periodontitis, on intestinal microbiota and atherosclerosis. MATERIALS AND METHODS: CFUs of live PG into the oral cavity of each mouse using a feeding needle five times a week for 3 weeks. Atherosclerotic lesions of the aortae were measured, a
Atherosclerosis, the major pathology of cardiovascular disease, is caused by multiple factors involving psychological stress. Corticotropin-releasing hormone (CRH), which is released by neurosecretory cells in the hypothalamus, peripheral nerve terminals and epithelial cells, regulates various stress-related responses. Our current study aimed to verify the role of CRH in macrophage foam cell formation, the initial critical stage of atherosclerosis. Our quantitative real-time reverse transcriptas
Oxidized LDL (oxLDL) performs critical roles in atherosclerosis by inducing macrophage foam cell formation and promoting inflammation. There have been reports showing that oxLDL modulates macrophage cytoskeletal functions for oxLDL uptake and trapping, however, the precise mechanism has not been clearly elucidated. Our study examined the effect of oxLDL on non-muscle myosin heavy chain IIA (MHC-IIA) in macrophages. We demonstrated that oxLDL induces phosphorylation of MHC-IIA (Ser1917) in perito
The purpose of this study was to examine the mediating effect of perceptions regarding the importance of patient safety management in the relationship between incident reporting attitudes and patient safety care activities for nurses in small-and medium-sized general hospitals. The objective was to provide a basis for planning tailored training programs aimed at improving patient safety care activities. Methods : This study was conducted with 187 participants in small-and medium-sized general ho
Vimentin is a type III intermediate filament protein expressed in cells of mesenchymal origin. Vimentin has been thought to function mainly as a structural protein and roles of vimentin in other cellular processes have not been extensively studied. Our current study aims to reveal functions of vimentin in macrophage foam cell formation, the critical stage of atherosclerosis. We demonstrated that vimentin null ( Vim –/ – ) mouse peritoneal macrophages take up less oxidized LDL (oxLDL) than viment
본 연구는 다슬기(Semisulcospira libertine) 열수 추출물이 D-galactosamine에 의해 급성 간독성이 유도된 흰쥐에 미치는 보호 효과를 조사하였다. 다슬기 열수 추출물은 D-galactosamine에 의해 유발된 간 조직 내 국소적 지방변성과 염증세포 침윤을 크게 완화하여 대조군과 유사하게 보호하는 경향을 보였다. 또한 다슬기 열수 추출물을 처리한 실험군은 간 손상 지표 효소인 AST와 ALT, LDH 및 ALP의 활성이 대조군 수준으로 유지되었으며 간조직 내 지질함량과 과산화지질함량이 감소되는 것으로 나타나 다슬기 열수 추출물이 D-galactosamine으로 인한 혈중 효소 활성과 조직 내 지질함량을 개선하는 것으로 조사되었다. 또한 다슬기 열수 추출물을 처리한 실험군은 염증반응을 촉진시켜 조직 상해 및 괴사를 유도하는 TNF-α의 발현을 억제하고 있어 염증 반응에서 세포 손상을 감소시키는 데 관여하는 것으로 나타났다. 따라서 다슬기 열수 추
Oxidized LDL (oxLDL) performs critical roles in atherosclerosisby inducing macrophage foam cell formation and promotinginflammation. There have been reports showing that oxLDLmodulates macrophage cytoskeletal functions for oxLDLuptake and trapping, however, the precise mechanism has notbeen clearly elucidated. Our study examined the effect ofoxLDL on non-muscle myosin heavy chain IIA (MHC-IIA) inmacrophages. We demonstrated that oxLDL induces phosphorylationof MHC-IIA (Ser1917) in peritoneal mac
본 연구는 산겨릅나무 세포배양 추출물이 D-galactosamine에 의해 유발된 간독성에 따른 보호 효과를 살펴보았다. 간 조직 내 국소적 지방 변성과 염증세포 침윤은 산겨릅나무 세포배양 추출물을 처리한 실험군에서 크게 감소되는 경향을 보였다. 또한 산겨릅나무 세포배양 추출물을 처리한 실험군은 간 손상에 의해 급격히 증가된 AST와 ALT, LDH 및 ALP의 활성과 조직 내 지질함량과 과산화지질함량이 감소되는 것으로 나타나 산겨릅나무 세포배양 추출물이 D-galactosamine으로 인한 혈중 효소활성과 조직 내 지질함량을 개선하는 것으로 조사되었다. 이와 더불어 산겨릅나무 세포배양 추출물을 처리한 실험군은 염증반응을 촉진시켜 조직 상해 및 괴사를 유도하는 TNF-α의 발현 수준이 간독성을 유발한 실험군에 비해 낮은 것으로 확인되었고 항산화효소의 활성을 효과적으로 조절하였다. 이러한 결과로 미루어 보아 산겨릅나무 세포배양 추출물은 D-galactosamine에 의한 조직 괴사를
The purpose of the study was to investigate nutritional status of chronic obstructive pulmonary disease (COPD) patients and to find out the differences according to the stages of disease. From March to October, 2006, 41 stable male patients of mild to severe COPD patients were recruited from Seoul National University hospital. The patients' of body weight and fat free mass were assessed by bioelectrical impedance analysis. The nutritional status of the patients was also assessed by 3-day recall,
Research Areas
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