Lipidomic analysis of urinary exosomes from hereditary α‐tryptasemia patients and healthy volunteers

• Published in: FASEB bioAdvances Vol. 1; no. 10; pp. 624 - 638
• Main Authors: Glover, Sarah C., Nouri, Mohammad‐Zaman, Tuna, Kubra M., Mendoza Alvarez, Lybil B., Ryan, Lisa K., Shirley, James F., Tang, Ying, Denslow, Nancy D., Alli, Abdel A.
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.10.2019; John Wiley and Sons Inc; Wiley
• Subjects: Biosynthesis; Cell differentiation; Cell interactions; Cell signaling; Cholesterol; Enzymes; Exosomes; Genetic disorders; glycerolipids; glycerophospholipids; hereditary α‐tryptasemia; Investigations; Irritable bowel syndrome; Laboratories; Lipid composition; lipidomics; Lipids; Liquid chromatography; Mass spectroscopy; Phospholipids; Species; Sphingolipids; Sterols; urinary exosomes; Urine; glycerolipids; urinary exosomes; sterols; lipidomics; glycerophospholipids; hereditary α-tryptasemia
• ISSN: 2573-9832; 2573-9832
• DOI: 10.1096/fba.2019-00030

Exosomes are nano‐sized vesicles that are involved in various biological processes including cell differentiation, proliferation, signaling, and intercellular communication. Urinary exosomes were isolated from a cohort of hereditary α‐tryptasemia (HαT) patients and from healthy volunteers. There was a greater number of exosomes isolated from the urine in the HαT group compared to the control volunteers. Here, we investigated the differences in both lipid classes and lipid species within urinary exosomes of the two groups. Lipids were extracted from urinary exosomes and subjected to liquid chromatography mass spectrometry using a targeted approach. Various molecular species of glycerophospholipids, glycerolipids, and sterols were significantly reduced in HαT patients. Out of a possible 1127 lipids, 521 lipid species were detected, and relative quantities were calculated. Sixty‐four lipids were significantly reduced in urinary exosomes of HαT patients compared to controls. All significantly reduced sphingolipids and most of the phospholipids were saturated or mono‐unsaturated lipids. These results suggest exosome secretion is augmented in HαT patients and the lipids within these exosomes may be involved in various biological processes. The unique lipid composition of urinary exosomes from HαT patients will contribute to our understanding of the biochemistry of this disease.