دورية أكاديمية

Composition-function analysis of HDL subpopulations: influence of lipid composition on particle functionality.

التفاصيل البيبلوغرافية
العنوان: Composition-function analysis of HDL subpopulations: influence of lipid composition on particle functionality.
المؤلفون: Niisuke K; Cardiovascular Nutrition Laboratory, Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111., Kuklenyik Z; Centers for Disease Control and Prevention, Division of Laboratory Sciences, Atlanta, GA 30341., Horvath KV; Cardiovascular Nutrition Laboratory, Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111., Gardner MS; Centers for Disease Control and Prevention, Division of Laboratory Sciences, Atlanta, GA 30341., Toth CA; Centers for Disease Control and Prevention, Division of Laboratory Sciences, Atlanta, GA 30341., Asztalos BF; Cardiovascular Nutrition Laboratory, Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111.
المصدر: Journal of lipid research [J Lipid Res] 2020 Mar; Vol. 61 (3), pp. 306-315. Date of Electronic Publication: 2020 Jan 17.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 0376606 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1539-7262 (Electronic) Linking ISSN: 00222275 NLM ISO Abbreviation: J Lipid Res Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : [New York] : Elsevier
Original Publication: Memphis, Lipid Research, inc.
مواضيع طبية MeSH: Coronary Disease/*blood , Lipid Droplets/*chemistry , Lipoproteins, HDL/*blood, Adult ; Aged ; Coronary Disease/metabolism ; Female ; Humans ; Lipid Droplets/metabolism ; Lipoproteins, HDL/metabolism ; Male ; Middle Aged ; Particle Size ; Young Adult
مستخلص: The composition-function relationship of HDL particles and its effects on the mechanisms driving coronary heart disease (CHD) is poorly understood. We tested the hypothesis that the functionality of HDL particles is significantly influenced by their lipid composition. Using a novel 3D-separation method, we isolated five different-sized HDL subpopulations from CHD patients who had low preβ-1 functionality (low-F) (ABCA1-dependent cholesterol-efflux normalized for preβ-1 concentration) and controls who had either low-F or high preβ-1 functionality (high-F). Molecular numbers of apoA-I, apoA-II, and eight major lipid classes were determined in each subpopulation by LC-MS. The average number of lipid molecules decreased from 422 in the large spherical α-1 particles to 57 in the small discoid preβ-1 particles. With decreasing particle size, the relative concentration of free cholesterol (FC) decreased in α-mobility but not in preβ-1 particles. Preβ-1 particles contained more lipids than predicted; 30% of which were neutral lipids (cholesteryl ester and triglyceride), indicating that these particles were mainly remodeled from larger particles not newly synthesized. There were significant correlations between HDL-particle functionality and the concentrations of several lipids. Unexpectedly, the phospholipid:FC ratio was significantly correlated with large-HDL-particle functionality but not with preβ-1 functionality. There was significant positive correlation between particle functionality and total lipids in high-F controls, indicating that the lipid-binding capacity of apoA-I plays a major role in the cholesterol efflux capacity of HDL particles. Functionality and lipid composition of HDL particles are significantly correlated and probably both are influenced by the lipid-binding capacity of apoA-I.
References: Circulation. 1989 Jan;79(1):8-15. (PMID: 2642759)
Arterioscler Thromb Vasc Biol. 2000 Dec;20(12):2670-6. (PMID: 11116070)
Arterioscler Thromb Vasc Biol. 2013 Dec;33(12):2715-23. (PMID: 24092747)
N Engl J Med. 2011 Dec 15;365(24):2255-67. (PMID: 22085343)
JAMA Cardiol. 2016 Jul 1;1(4):413-23. (PMID: 27438317)
Arterioscler Thromb Vasc Biol. 2004 Nov;24(11):2181-7. (PMID: 15388521)
J Lipid Res. 2001 Aug;42(8):1308-17. (PMID: 11483633)
Arterioscler Thromb Vasc Biol. 2005 Oct;25(10):2185-91. (PMID: 16123324)
Circulation. 1999 Feb 16;99(6):736-43. (PMID: 9989957)
J Am Soc Mass Spectrom. 2017 Nov;28(11):2319-2329. (PMID: 28801822)
J Lipid Res. 2005 Oct;46(10):2246-53. (PMID: 16061948)
N Engl J Med. 2012 Nov 29;367(22):2089-99. (PMID: 23126252)
N Engl J Med. 2011 Jan 13;364(2):127-35. (PMID: 21226578)
Arterioscler Thromb Vasc Biol. 2018 Sep;38(9):2007-2015. (PMID: 30002062)
Arterioscler Thromb Vasc Biol. 2003 May 1;23(5):847-52. (PMID: 12637338)
JAMA. 2007 Feb 7;297(5):499-508. (PMID: 17284700)
Arterioscler Thromb Vasc Biol. 2002 Sep 1;22(9):1482-8. (PMID: 12231570)
J Lipid Res. 2013 Nov;54(11):2950-63. (PMID: 23543772)
Lancet Diabetes Endocrinol. 2015 Jul;3(7):507-13. (PMID: 26025389)
J Appl Lab Med. 2017 Sep 1;2(2):186-200. (PMID: 32630971)
Lancet. 2005 Nov 26;366(9500):1849-61. (PMID: 16310551)
N Engl J Med. 2014 Dec 18;371(25):2383-93. (PMID: 25404125)
J Proteomics. 2017 Jan 6;150:258-267. (PMID: 27667389)
J Biol Chem. 2013 Aug 9;288(32):23150-60. (PMID: 23836906)
Sci Rep. 2016 Jan 18;6:19249. (PMID: 26778677)
J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Jun 15;1118-1119:137-147. (PMID: 31035135)
Chem Phys Lipids. 2008 Sep;155(1):57-62. (PMID: 18611396)
معلومات مُعتمدة: R01 HL117933 United States HL NHLBI NIH HHS
فهرسة مساهمة: Keywords: high density lipoprotein; lipid ratios; phospholipids; pre-beta
المشرفين على المادة: 0 (Lipoproteins, HDL)
تواريخ الأحداث: Date Created: 20200119 Date Completed: 20210603 Latest Revision: 20240328
رمز التحديث: 20240329
مُعرف محوري في PubMed: PMC7053829
DOI: 10.1194/jlr.RA119000258
PMID: 31953305
قاعدة البيانات: MEDLINE
الوصف
تدمد:1539-7262
DOI:10.1194/jlr.RA119000258