Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic intervention
The removal of excess cholesterol from the body by High-density lipoprotein (HDL) in a process termed reverse cholesterol transport (RCT) has long been proposed to play a critical role in reduction of the lipid burden in arterial wall atherosclerotic lesions. While HDL-cholesterol levels are associa...
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| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2025-07-01
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| Series: | Frontiers in Cardiovascular Medicine |
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fcvm.2025.1608384/full |
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| author | Martin P. Playford Edward B. Neufeld Rafael Zubirán Alan T. Remaley |
| author_facet | Martin P. Playford Edward B. Neufeld Rafael Zubirán Alan T. Remaley |
| author_sort | Martin P. Playford |
| collection | DOAJ |
| description | The removal of excess cholesterol from the body by High-density lipoprotein (HDL) in a process termed reverse cholesterol transport (RCT) has long been proposed to play a critical role in reduction of the lipid burden in arterial wall atherosclerotic lesions. While HDL-cholesterol levels are associated with decreased cardiovascular risk and considered to be “good-cholesterol”, clinical studies using HDL-raising therapies to potentially enhance RCT have consistently produced disappointing results. In this mini review we evaluate the effects of human disease on RCT along with the changes in this process upon various therapeutic interventions. Despite the importance of assay standardization, the major method for monitoring RCT has relied upon the cholesterol efflux capacity (CEC) assay, a highly-difficult and tedious cell culture assay, which is low-throughput and only suitable for research studies. Hence, we also briefly review several new methods to measure RCT both in vitro and in vivo, along with new cell-free alternative RCT assays, which have the potential to be developed into routine automated diagnostic assay. The benefits of HDL may yet be revealed by the use of these new high-throughput RCT assays perhaps as a screening tool for novel RCT boosting agents or as new biomarkers for cardiovascular disease risk. |
| format | Article |
| id | doaj-art-e6bdd0831a044602b5d40e07bd3f1565 |
| institution | Kabale University |
| issn | 2297-055X |
| language | English |
| publishDate | 2025-07-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Cardiovascular Medicine |
| spelling | doaj-art-e6bdd0831a044602b5d40e07bd3f15652025-08-20T03:50:26ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2025-07-011210.3389/fcvm.2025.16083841608384Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic interventionMartin P. Playford0Edward B. Neufeld1Rafael Zubirán2Alan T. Remaley3Section of Inflammation and Cardiometabolic Diseases, National Heart, Lung and Blood Institute, NIH, Bethesda, MD, United StatesLipoprotein Metabolism Laboratory, National Heart, Lung, and Blood Institute (NHLBI), NIH, Bethesda, MD, United StatesLipoprotein Metabolism Laboratory, National Heart, Lung, and Blood Institute (NHLBI), NIH, Bethesda, MD, United StatesLipoprotein Metabolism Laboratory, National Heart, Lung, and Blood Institute (NHLBI), NIH, Bethesda, MD, United StatesThe removal of excess cholesterol from the body by High-density lipoprotein (HDL) in a process termed reverse cholesterol transport (RCT) has long been proposed to play a critical role in reduction of the lipid burden in arterial wall atherosclerotic lesions. While HDL-cholesterol levels are associated with decreased cardiovascular risk and considered to be “good-cholesterol”, clinical studies using HDL-raising therapies to potentially enhance RCT have consistently produced disappointing results. In this mini review we evaluate the effects of human disease on RCT along with the changes in this process upon various therapeutic interventions. Despite the importance of assay standardization, the major method for monitoring RCT has relied upon the cholesterol efflux capacity (CEC) assay, a highly-difficult and tedious cell culture assay, which is low-throughput and only suitable for research studies. Hence, we also briefly review several new methods to measure RCT both in vitro and in vivo, along with new cell-free alternative RCT assays, which have the potential to be developed into routine automated diagnostic assay. The benefits of HDL may yet be revealed by the use of these new high-throughput RCT assays perhaps as a screening tool for novel RCT boosting agents or as new biomarkers for cardiovascular disease risk.https://www.frontiersin.org/articles/10.3389/fcvm.2025.1608384/fullcholesterolABCA1ApoA-1inflammationreverse cholesterol transport (RCT) |
| spellingShingle | Martin P. Playford Edward B. Neufeld Rafael Zubirán Alan T. Remaley Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic intervention Frontiers in Cardiovascular Medicine cholesterol ABCA1 ApoA-1 inflammation reverse cholesterol transport (RCT) |
| title | Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic intervention |
| title_full | Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic intervention |
| title_fullStr | Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic intervention |
| title_full_unstemmed | Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic intervention |
| title_short | Reverse cholesterol transport: current assay methods, alterations with disease and response to therapeutic intervention |
| title_sort | reverse cholesterol transport current assay methods alterations with disease and response to therapeutic intervention |
| topic | cholesterol ABCA1 ApoA-1 inflammation reverse cholesterol transport (RCT) |
| url | https://www.frontiersin.org/articles/10.3389/fcvm.2025.1608384/full |
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