Early Pro-Inflammatory Remodeling of HDL Proteome in a Model of Diet-Induced Obesity: 2H2O-Metabolic Labeling-Based Kinetic Approach

Autor: Li Lin, Mirjavid Aghayev, Prabodh Sadana, Serguei Ilchenko, Takhar Kasumov
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
Male
Proteomics
Proteome
030204 cardiovascular system & hematology
Mass Spectrometry
lcsh:Chemistry
Mice
0302 clinical medicine
Non-alcoholic Fatty Liver Disease
insulin resistance
Protein Interaction Mapping
Protein Interaction Maps
lcsh:QH301-705.5
Spectroscopy
Fatty liver
General Medicine
Computer Science Applications
high-fat diet
Factor H
acute-phase proteins
Disease Susceptibility
Lipoproteins
HDL

medicine.medical_specialty
diet-induced obesity
Complement factor I
high-density lipoprotein
Diet
High-Fat

Complement factor B
Catalysis
Article
Inorganic Chemistry
03 medical and health sciences
Insulin resistance
Internal medicine
NAFLD
medicine
Animals
Obesity
Physical and Theoretical Chemistry
Molecular Biology
business.industry
Organic Chemistry
dyslipidemia
nutritional and metabolic diseases
medicine.disease
Diet
Disease Models
Animal

030104 developmental biology
Endocrinology
lcsh:Biology (General)
lcsh:QD1-999
inflammation
Steatosis
business
proteome dynamics
Dyslipidemia
Biomarkers
Lipoprotein
Zdroj: International Journal of Molecular Sciences
Volume 21
Issue 20
International Journal of Molecular Sciences, Vol 21, Iss 7472, p 7472 (2020)
ISSN: 1422-0067
DOI: 10.3390/ijms21207472
Popis: Mice fed a high-fat diet for 12 weeks or longer develop hyperglycemia, insulin resistance, dyslipidemia, and fatty liver. Additionally, a high-fat diet induces inflammation that remodels and affects the anti-inflammatory and antiatherogenic property of the high-density lipoprotein (HDL). However, the precise time course of metabolic disease progression and HDL remodeling remains unclear. Short-term (four weeks) high-fat feeding (60% fat calories) was performed in wild-type male C57BL/6J mice to gain insights into the early metabolic disease processes in conjunction with a HDL proteome dynamics analysis using a heavy water metabolic labeling approach. The high-fat diet-fed mice developed hyperglycemia, impaired glucose tolerance, hypercholesterolemia without hypertriglyceridemia or hepatic steatosis. A plasma HDL proteome dynamics analysis revealed increased turnover rates (and reduced half-lives) of several acute-phase response proteins involved in innate immunity, including complement C3 (12.77 ±
0.81 vs. 9.98 ±
1.20 h, p <
0.005), complement factor B (12.71 ±
1.01 vs. 10.85 ±
1.04 h, p <
0.05), complement Factor H (19.60 ±
1.84 vs. 16.80 ±
1.58 h, p <
0.05), and complement factor I (25.25 ±
1.29 vs. 19.88 ±
1.50 h, p <
0.005). Our findings suggest that an early immune response-induced inflammatory remodeling of the plasma HDL proteome precedes the diet-induced steatosis and dyslipidemia.
Databáze: OpenAIRE
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