Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors

PLoS One. 2017 Aug 2;12(8):e0180772. doi: 10.1371/journal.pone.0180772. eCollection 2017.

Abstract

Cholesteryl ester transfer protein (CETP) is a plasma protein that mediates bidirectional transfers of cholesteryl esters and triglycerides between low-density lipoproteins and high-density lipoproteins (HDL). Because low levels of plasma CETP are associated with increased plasma HDL-cholesterol, therapeutic inhibition of CETP activity is considered an attractive strategy for elevating plasma HDL-cholesterol, thereby hoping to reduce the risk of cardiovascular disease. Interestingly, only a few laboratory animals, such as rabbits, guinea pigs, and hamsters, have plasma CETP activity, whereas mice and rats do not. It is not known whether all CETPs in these laboratory animals are functionally similar to human CETP. In the current study, we compared plasma CETP activity and characterized the plasma lipoprotein profiles of these animals. Furthermore, we studied the three CETP molecular structures, physicochemical characteristics, and binding properties with known CETP inhibitors in silico. Our results showed that rabbits exhibited higher CETP activity than guinea pigs and hamsters, while these animals had different lipoprotein profiles. CETP inhibitors can inhibit rabbit and hamster CETP activity in a similar manner to human CETP. Analysis of CETP molecules in silico revealed that rabbit and hamster CETP showed many features that are similar to human CETP. These results provide novel insights into understanding CETP functions and molecular properties.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Anticholesteremic Agents / chemistry
  • Anticholesteremic Agents / metabolism*
  • Benzodiazepines / chemistry
  • Benzodiazepines / metabolism
  • Binding Sites
  • Cholesterol / blood
  • Cholesterol Ester Transfer Proteins / antagonists & inhibitors
  • Cholesterol Ester Transfer Proteins / classification
  • Cholesterol Ester Transfer Proteins / metabolism*
  • Cholesterol, HDL / blood
  • Cricetinae
  • Guinea Pigs
  • Lipoproteins, LDL / blood
  • Male
  • Molecular Dynamics Simulation
  • Oxazolidinones / chemistry
  • Oxazolidinones / metabolism
  • Phylogeny
  • Protein Structure, Tertiary
  • Rabbits
  • Triglycerides / blood

Substances

  • Anticholesteremic Agents
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • Lipoproteins, LDL
  • Oxazolidinones
  • Triglycerides
  • Benzodiazepines
  • evacetrapib
  • Cholesterol
  • anacetrapib

Grants and funding

This work was supported by the National Natural Science Foundation of China (grant no. 21272017, 20802006 to ZL & 81173470/H2903 to JX), Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports and Technology, Japan (22390068, 25670190 and 15H04718 to JF), and the Natural Science Foundation of Shaanxi Province (2017JZ028). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.