Abstract

Background and aimsAdipose tissue plays a pivotal role in storing excess fat and its composition reflects the history of person’s lifestyle and metabolic health. Broad profiling of lipids with mass spectrometry has potential for uncovering new knowledge on the pathology of obesity, metabolic syndrome, diabetes and other related conditions. Here, we developed a lipidomic method for analyzing human subcutaneous adipose biopsies. We applied the method to four body areas to understand the differences in lipid composition between these areas.Materials and methodsAdipose tissue biopsies from 10 participants were analyzed using ultra-high-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry. The sample preparation optimization included the optimization of the lipid extraction, the sample amount and the sample dilution factor to detect lipids in an appropriate concentration range. Lipidomic analyses were performed for adipose tissue collected from the abdomen, breast, thigh and lower back. Differences in lipid levels between tissues were visualized with heatmaps.ResultsLipidomic analysis on human adipose biopsies lead to the identification of 186lipids in 2 mg of sample. Technical variation of the lipid-class specific internal standards were below 5%, thus indicating acceptable repeatability. Triacylglycerols were highly represented in the adipose tissue samples, and lipids from 13 lipid classes were identified. Long polyunsaturated triacylglycerols in higher levels in thigh (q<0.05), when compared with the abdomen, breast and lower back, indicating that the lipidome was area-specific.ConclusionThe method presented here is suitable for the analysis of lipid profiles in 2 mg of adipose tissue. The amount of fat across the body is important for health but we argue that also the distribution and the particular profile of the lipidome may be relevant for metabolic outcomes. We suggest that the method presented in this paper could be useful for detecting such aberrations.

Highlights

  • Adipocytes are cells that form and store lipids in adipose tissue, they play a major role in energy homeostasis [1,2]

  • Adipose tissue biopsies from 10 participants were analyzed using ultra-high-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry

  • Obesity, which is characterized by increased storage of lipids in adipose tissue and modification of the metabolic functions of adipocytes, is a risk factor for several metabolic diseases, including atherosclerosis, cardiovascular ischemic disease, hypertension, hyperglycemia and insulin resistance in type 2 diabetes[1,3,4,5,6,7]

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Summary

Introduction

Adipocytes are cells that form and store lipids in adipose tissue, they play a major role in energy homeostasis [1,2]. Obesity, which is characterized by increased storage of lipids in adipose tissue and modification of the metabolic functions of adipocytes, is a risk factor for several metabolic diseases, including atherosclerosis, cardiovascular ischemic disease, hypertension, hyperglycemia and insulin resistance in type 2 diabetes[1,3,4,5,6,7]. The molecular composition of adipose tissue may reveal its functionality and links to metabolic disease[8,2]. Global lipidomic analysis of multiple areas of adipose tissue may lead to a better understanding of metabolism in disease[10,11]. Adipose tissue plays a pivotal role in storing excess fat and its composition reflects the history of person’s lifestyle and metabolic health. We applied the method to four body areas to understand the differences in lipid composition between these areas.

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