Lipidomic profiling of adipose tissue reveals an inflammatory signature in cancer-related and primary Lymphedema
Sedger, LM
Tull, DL
McConville, MJ
De Souza, DP
Rupasinghe, TWT
Williams, SJ
Dayalan, S
Lanzer, D
Mackie, H
Lam, TC
Boyages, J
Tull, DL
McConville, MJ
De Souza, DP
Rupasinghe, TWT
Williams, SJ
Dayalan, S
Lanzer, D
Mackie, H
Lam, TC
Boyages, J
- Publication Type:
- Journal Article
- Citation:
- PLoS ONE, 2016, 11 (5)
- Issue Date:
- 2016-05-01
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© 2016 Sedger et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Cancer-related and primary lymphedema (LE) are associated with the production of adipose tissue (AT). Nothing is known, however, about the lipid-based molecules that comprise LE AT. We therefore analyzed lipid molecules in lipoaspirates and serum obtained from LE patients, and compared them to lipoaspirates from cosmetic surgery patients and healthy control cohort serum. LE patient serum analysis demonstrated that triglycerides, HDL- and LDL-cholesterol and lipid transport molecules remained within the normal range, with no alterations in individual fatty acids. The lipidomic analysis also identified 275 lipid-based molecules, including triacylglycerides, diacylglycerides, fatty acids and phospholipids in AT oil and fat. Although the majority of lipid molecules were present in a similar abundance in LE and non-LE samples, there were several small changes: increased C20:5-containing triacylglycerides, reduced C10:0 caprinic and C24:1 nervonic acids. LE AT oil also contained a signature of increased cyclopropane-type fatty acids and inflammatory mediators arachidonic acid and ceramides. Interestingly C20:5 and C22:6 omega-3-type lipids are increased in LE AT, correlating with LE years. Hence, LE AT has a normal lipid profile containing a signature of inflammation and omega-3-lipids. It remains unclear, however, whether these differences reflect a small-scale global metabolic disturbance or effects within localised inflammatory foci.
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