A Novel Relative High-Density Lipoprotein Index to Predict the Structural Changes in High-Density Lipoprotein and Its Ability to Inhibit Endothelial–Mesenchymal Transition
Therapeutic elevation of high-density lipoprotein (HDL) is thought to minimize atherogenesis in subjects with dyslipidemia. However, this is not the case in clinical practice. The function of HDL is not determined by its concentration in the plasma but by its specific structural components. We previ...
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Published in | International journal of molecular sciences Vol. 22; no. 10; p. 5210 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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14.05.2021
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ISSN | 1422-0067 1661-6596 1422-0067 |
DOI | 10.3390/ijms22105210 |
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Abstract | Therapeutic elevation of high-density lipoprotein (HDL) is thought to minimize atherogenesis in subjects with dyslipidemia. However, this is not the case in clinical practice. The function of HDL is not determined by its concentration in the plasma but by its specific structural components. We previously identified an index for the prediction of HDL functionality, relative HDL (rHDL) index, and preliminarily explored that dysfunctional HDL (rHDL index value > 2) failed to rescue the damage to endothelial progenitor cells (EPCs). To confirm the effectiveness of the rHDL index for predicting HDL functions, here we evaluated the effects of HDL from patients with different rHDL index values on the endothelial–mesenchymal transition (EndoMT) of EPCs. We also analyzed the lipid species in HDL with different rHDL index values and investigated the structural differences that affect HDL functions. The results indicate that HDL from healthy adults and subjects with an rHDL index value < 2 protected transforming growth factor (TGF)-β1-stimulated EndoMT by modulating Smad2/3 and Snail activation. HDL from subjects with an rHDL index value > 2 failed to restore the functionality of TGF-β1-treated EPCs. Lipidomic analysis demonstrated that HDL with different rHDL index values may differ in the composition of triglycerides, phosphatidylcholine, and phosphatidylinositol. In conclusion, we confirmed the applicability of the rHDL index value to predict HDL function and found structural differences that may affect the function of HDL, which warrants further in-depth studies. |
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AbstractList | Therapeutic elevation of high-density lipoprotein (HDL) is thought to minimize atherogenesis in subjects with dyslipidemia. However, this is not the case in clinical practice. The function of HDL is not determined by its concentration in the plasma but by its specific structural components. We previously identified an index for the prediction of HDL functionality, relative HDL (rHDL) index, and preliminarily explored that dysfunctional HDL (rHDL index value > 2) failed to rescue the damage to endothelial progenitor cells (EPCs). To confirm the effectiveness of the rHDL index for predicting HDL functions, here we evaluated the effects of HDL from patients with different rHDL index values on the endothelial–mesenchymal transition (EndoMT) of EPCs. We also analyzed the lipid species in HDL with different rHDL index values and investigated the structural differences that affect HDL functions. The results indicate that HDL from healthy adults and subjects with an rHDL index value < 2 protected transforming growth factor (TGF)-β1-stimulated EndoMT by modulating Smad2/3 and Snail activation. HDL from subjects with an rHDL index value > 2 failed to restore the functionality of TGF-β1-treated EPCs. Lipidomic analysis demonstrated that HDL with different rHDL index values may differ in the composition of triglycerides, phosphatidylcholine, and phosphatidylinositol. In conclusion, we confirmed the applicability of the rHDL index value to predict HDL function and found structural differences that may affect the function of HDL, which warrants further in-depth studies. Therapeutic elevation of high-density lipoprotein (HDL) is thought to minimize atherogenesis in subjects with dyslipidemia. However, this is not the case in clinical practice. The function of HDL is not determined by its concentration in the plasma but by its specific structural components. We previously identified an index for the prediction of HDL functionality, relative HDL (rHDL) index, and preliminarily explored that dysfunctional HDL (rHDL index value > 2) failed to rescue the damage to endothelial progenitor cells (EPCs). To confirm the effectiveness of the rHDL index for predicting HDL functions, here we evaluated the effects of HDL from patients with different rHDL index values on the endothelial-mesenchymal transition (EndoMT) of EPCs. We also analyzed the lipid species in HDL with different rHDL index values and investigated the structural differences that affect HDL functions. The results indicate that HDL from healthy adults and subjects with an rHDL index value < 2 protected transforming growth factor (TGF)-β1-stimulated EndoMT by modulating Smad2/3 and Snail activation. HDL from subjects with an rHDL index value > 2 failed to restore the functionality of TGF-β1-treated EPCs. Lipidomic analysis demonstrated that HDL with different rHDL index values may differ in the composition of triglycerides, phosphatidylcholine, and phosphatidylinositol. In conclusion, we confirmed the applicability of the rHDL index value to predict HDL function and found structural differences that may affect the function of HDL, which warrants further in-depth studies.Therapeutic elevation of high-density lipoprotein (HDL) is thought to minimize atherogenesis in subjects with dyslipidemia. However, this is not the case in clinical practice. The function of HDL is not determined by its concentration in the plasma but by its specific structural components. We previously identified an index for the prediction of HDL functionality, relative HDL (rHDL) index, and preliminarily explored that dysfunctional HDL (rHDL index value > 2) failed to rescue the damage to endothelial progenitor cells (EPCs). To confirm the effectiveness of the rHDL index for predicting HDL functions, here we evaluated the effects of HDL from patients with different rHDL index values on the endothelial-mesenchymal transition (EndoMT) of EPCs. We also analyzed the lipid species in HDL with different rHDL index values and investigated the structural differences that affect HDL functions. The results indicate that HDL from healthy adults and subjects with an rHDL index value < 2 protected transforming growth factor (TGF)-β1-stimulated EndoMT by modulating Smad2/3 and Snail activation. HDL from subjects with an rHDL index value > 2 failed to restore the functionality of TGF-β1-treated EPCs. Lipidomic analysis demonstrated that HDL with different rHDL index values may differ in the composition of triglycerides, phosphatidylcholine, and phosphatidylinositol. In conclusion, we confirmed the applicability of the rHDL index value to predict HDL function and found structural differences that may affect the function of HDL, which warrants further in-depth studies. |
Author | Lin, Feng-Yen Tsai, Yi-Ting Tung, Yu-Tang Huang, Chun-Yao Lin, Yi-Wen Li, Chi-Yuan Lin, Shing-Jong Shih, Chun-Ming Chen, Yung-Hsiang Lin, Cheng-Yen |
AuthorAffiliation | 7 Graduate Institute of Integrated Medicine, China Medical University, Taichung 406, Taiwan; yhchen@mail.cmu.edu.tw 10 Division of Cardiovascular Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei 115, Taiwan 9 Healthcare Information and Management Department, Ming Chuan University, Taoyuan 333, Taiwan; a684094@ms28.hinet.net 1 Taipei Heart Institute, Taipei Medical University, Taipei 110, Taiwan; g870905@tmu.edu.tw (F.-Y.L.); cmshih53@tmu.edu.tw (C.-M.S.); sjlin@tmu.edu.tw (S.-J.L.) 5 Graduate Institute of Biotechnology, National Chung Hsing University, Taichung 238, Taiwan; peggytung@nchu.edu.tw 8 Department of Psychology, College of Medical and Health Science, Asia University, Taichung 413, Taiwan 3 Division of Cardiology, Department of Internal Medicine and Cardiovascular Research Center, Taipei Medical University Hospital, Taipei 110, Taiwan 4 Institute of Oral Biology, National Yang Ming Chiao Tung University, Hsinchu 300, Taiwan; ywlin@ym.edu.tw 2 Department |
AuthorAffiliation_xml | – name: 5 Graduate Institute of Biotechnology, National Chung Hsing University, Taichung 238, Taiwan; peggytung@nchu.edu.tw – name: 8 Department of Psychology, College of Medical and Health Science, Asia University, Taichung 413, Taiwan – name: 4 Institute of Oral Biology, National Yang Ming Chiao Tung University, Hsinchu 300, Taiwan; ywlin@ym.edu.tw – name: 3 Division of Cardiology, Department of Internal Medicine and Cardiovascular Research Center, Taipei Medical University Hospital, Taipei 110, Taiwan – name: 1 Taipei Heart Institute, Taipei Medical University, Taipei 110, Taiwan; g870905@tmu.edu.tw (F.-Y.L.); cmshih53@tmu.edu.tw (C.-M.S.); sjlin@tmu.edu.tw (S.-J.L.) – name: 6 Department of Anesthesiology and Graduate Institute of Clinical Medical Science, China Medical University and Hospital, Taichung 406, Taiwan; cyli168@gmail.com – name: 2 Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan – name: 7 Graduate Institute of Integrated Medicine, China Medical University, Taichung 406, Taiwan; yhchen@mail.cmu.edu.tw – name: 9 Healthcare Information and Management Department, Ming Chuan University, Taoyuan 333, Taiwan; a684094@ms28.hinet.net – name: 10 Division of Cardiovascular Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei 115, Taiwan |
Author_xml | – sequence: 1 givenname: Feng-Yen orcidid: 0000-0002-4939-2899 surname: Lin fullname: Lin, Feng-Yen – sequence: 2 givenname: Yi-Wen surname: Lin fullname: Lin, Yi-Wen – sequence: 3 givenname: Chun-Ming surname: Shih fullname: Shih, Chun-Ming – sequence: 4 givenname: Shing-Jong surname: Lin fullname: Lin, Shing-Jong – sequence: 5 givenname: Yu-Tang surname: Tung fullname: Tung, Yu-Tang – sequence: 6 givenname: Chi-Yuan surname: Li fullname: Li, Chi-Yuan – sequence: 7 givenname: Yung-Hsiang orcidid: 0000-0002-8756-5113 surname: Chen fullname: Chen, Yung-Hsiang – sequence: 8 givenname: Cheng-Yen surname: Lin fullname: Lin, Cheng-Yen – sequence: 9 givenname: Yi-Ting surname: Tsai fullname: Tsai, Yi-Ting – sequence: 10 givenname: Chun-Yao surname: Huang fullname: Huang, Chun-Yao |
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SubjectTerms | Atherosclerosis Bone marrow Cardiovascular disease Cholesterol Cloning Diabetes Endothelium Gene expression High density lipoprotein Lipids Lipoproteins Morphology Nitric oxide Oxidative stress Protein expression Proteins Smooth muscle |
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Title | A Novel Relative High-Density Lipoprotein Index to Predict the Structural Changes in High-Density Lipoprotein and Its Ability to Inhibit Endothelial–Mesenchymal Transition |
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