Dysfunctional high density lipoprotein failed to rescue the function of oxidized low density lipoprotein-treated endothelial progenitor cells: a novel index for the prediction of HDL functionality

Chun Ming Shih, Feng Yen Lin, Jong Shiuan Yeh, Yi Wen Lin, Shih Hurng Loh, Nai Wen Tsao, Hironori Nakagami, Ryuichi Morishita, Tatsuya Sawamura, Chi Yuan Li, Cheng Yen Lin, Chun Yao Huang

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Lipid metabolic disorders play critical roles in atherogenesis. Traditionally, it has been suggested that reduced high density lipoprotein (HDL) levels might be an important morbidity indicator for cardiovascular diseases. Therefore, it has been argued that therapeutically raising HDL levels may reduce atherogenesis in patients with dyslipidemia. However, recent clinical trials to elevate serum HDL levels by pharmacologic approaches failed to demonstrate clinical efficacy. Thus, to investigate the functionality of HDL and to explore the possible clinical relevance as well as to define an effective indicator that can represent HDL function may provide another key and reference to disclose the clinical treatment of dyslipidemia. We analyzed the association between the data of dichlorofluorescein assay (assay the functionality of HDL), the effect of HDL on oxidized low density lipoprotein (oxLDL)-stimulated endothelial progenitor cells (EPCs) in vitro, levels of circulating EPCs, and ex vitro EPC colony forming units of each case, we defined the indicator (relative HDL index (RHDL index) = dichlorofluorescein assay result of each subject/dichlorofluorescein assay reading of our young healthy controls) that may represent functionality of HDL. HDL from healthy adults protected oxLDL-treated EPCs by modulating p38 mitogen-activated protein kinase and Rho activation and by promoting nitric oxide production. HDL from subject with RHDL index ≧2 also failed to restore the functionality of oxLDL-treated EPCs via cell-signaling pathways in vitro. The RHDL index significantly correlated with patients’ circulating EPC number or EPC colony forming units ex vivo. In conclusions, we explored the RHDL index as a score to predict a patient's EPC functions in vivo and ex vitro.

Original languageEnglish
Pages (from-to)17-32
Number of pages16
JournalTranslational Research
Volume205
DOIs
Publication statusPublished - Mar 1 2019

Keywords

  • ACS = acute coronary syndrome
  • ALT= alanine transaminase
  • APOI = apocynin
  • CAD = coronary artery disease
  • CETP = cholesterol ester transfer protein
  • DCFH-DA = 2′,7′-dichlorofluorescin diacetate
  • HDL = high density lipoprotein
  • HPODE = hydroperoxyoctadeca-9Z,11E-dienoic acid
  • MNC = mononuclear cell
  • NO = nitric oxide
  • PAH-AH = platelet-activating factor acetylhydrolase
  • PMA = phorbol 12-myristate 13-acetate
  • PON1 = paraoxonase-1
  • RHDL index = relative HDL index
  • TBARS = thiobarbituric acid reactive substance
  • TC = total cholesterol
  • TG = triglycerides
  • eNOS = endothelial nitric oxide synthase

ASJC Scopus subject areas

  • Public Health, Environmental and Occupational Health
  • Biochemistry, medical
  • Physiology (medical)

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