Cargando…

Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation

Abnormal cellular lipid metabolism has a very important role in the occurrence and progression of diabetic kidney disease (DKD). However, the lipid composition and differential expression by high glucose stimulation of renal tubular cells and their exosomes, which is a vital part of the development...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Weidong, Li, Tingting, Li, Zhijie, Wang, Hongmiao, Liu, Xiaodan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795806/
https://www.ncbi.nlm.nih.gov/pubmed/35165524
http://dx.doi.org/10.7150/ijms.67326
_version_ 1784641155208577024
author Wang, Weidong
Li, Tingting
Li, Zhijie
Wang, Hongmiao
Liu, Xiaodan
author_facet Wang, Weidong
Li, Tingting
Li, Zhijie
Wang, Hongmiao
Liu, Xiaodan
author_sort Wang, Weidong
collection PubMed
description Abnormal cellular lipid metabolism has a very important role in the occurrence and progression of diabetic kidney disease (DKD). However, the lipid composition and differential expression by high glucose stimulation of renal tubular cells and their exosomes, which is a vital part of the development of DKD, are largely unknown. In this study, based on targeted lipid analysis by isotope labeling and tandem mass spectrometry, a total of 421 and 218 lipid species were quantified in HK-2 cells and exosomes, respectively. More importantly, results showed that GM3 d18:1/22:0, GM3 d18:1/16:0, GM3 d18:0/16:0, GM3 d18:1/22:1 were significantly increased, while LPE18:1, LPE, CL66:4 (16:1), BMP36:3, CL70:7 (16:1), CL74:8 (16:1) were significantly decreased in high glucose-stimulated HK-2 cells. Also, PG36:1, FFA22:5, PC38:3, SM d18:1/16:1, CE-16:1, CE-18:3, CE-20:5, and CE-22:6 were significantly increased, while GM3 d18:1/24:1, GM3 were significantly decreased in exosomes secreted by high glucose-stimulated HK-2 cells. Furthermore, TAG, PC, CL were decreased significantly in the exosomes comparing with the HK-2 cells, and LPA18:2, LPI22:5, PG32:2, FFA16:1, GM3 d18:1/18:1, GM3 d18:1/20:1, GM3 d18:0/20:0, PC40:6p, TAG52:1(18:1), TAG52:0(18:0), CE-20:5, CE-20:4, CE-22:6 were only found in exosomes. In addition, the expression of PI4P in HK-2 cells decreased under a high glucose state. These data may be useful to provide new targets for exploring the mechanisms of DKD.
format Online
Article
Text
id pubmed-8795806
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-87958062022-02-13 Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation Wang, Weidong Li, Tingting Li, Zhijie Wang, Hongmiao Liu, Xiaodan Int J Med Sci Research Paper Abnormal cellular lipid metabolism has a very important role in the occurrence and progression of diabetic kidney disease (DKD). However, the lipid composition and differential expression by high glucose stimulation of renal tubular cells and their exosomes, which is a vital part of the development of DKD, are largely unknown. In this study, based on targeted lipid analysis by isotope labeling and tandem mass spectrometry, a total of 421 and 218 lipid species were quantified in HK-2 cells and exosomes, respectively. More importantly, results showed that GM3 d18:1/22:0, GM3 d18:1/16:0, GM3 d18:0/16:0, GM3 d18:1/22:1 were significantly increased, while LPE18:1, LPE, CL66:4 (16:1), BMP36:3, CL70:7 (16:1), CL74:8 (16:1) were significantly decreased in high glucose-stimulated HK-2 cells. Also, PG36:1, FFA22:5, PC38:3, SM d18:1/16:1, CE-16:1, CE-18:3, CE-20:5, and CE-22:6 were significantly increased, while GM3 d18:1/24:1, GM3 were significantly decreased in exosomes secreted by high glucose-stimulated HK-2 cells. Furthermore, TAG, PC, CL were decreased significantly in the exosomes comparing with the HK-2 cells, and LPA18:2, LPI22:5, PG32:2, FFA16:1, GM3 d18:1/18:1, GM3 d18:1/20:1, GM3 d18:0/20:0, PC40:6p, TAG52:1(18:1), TAG52:0(18:0), CE-20:5, CE-20:4, CE-22:6 were only found in exosomes. In addition, the expression of PI4P in HK-2 cells decreased under a high glucose state. These data may be useful to provide new targets for exploring the mechanisms of DKD. Ivyspring International Publisher 2022-01-24 /pmc/articles/PMC8795806/ /pubmed/35165524 http://dx.doi.org/10.7150/ijms.67326 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Weidong
Li, Tingting
Li, Zhijie
Wang, Hongmiao
Liu, Xiaodan
Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation
title Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation
title_full Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation
title_fullStr Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation
title_full_unstemmed Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation
title_short Differential lipidomics of HK-2 cells and exosomes under high glucose stimulation
title_sort differential lipidomics of hk-2 cells and exosomes under high glucose stimulation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795806/
https://www.ncbi.nlm.nih.gov/pubmed/35165524
http://dx.doi.org/10.7150/ijms.67326
work_keys_str_mv AT wangweidong differentiallipidomicsofhk2cellsandexosomesunderhighglucosestimulation
AT litingting differentiallipidomicsofhk2cellsandexosomesunderhighglucosestimulation
AT lizhijie differentiallipidomicsofhk2cellsandexosomesunderhighglucosestimulation
AT wanghongmiao differentiallipidomicsofhk2cellsandexosomesunderhighglucosestimulation
AT liuxiaodan differentiallipidomicsofhk2cellsandexosomesunderhighglucosestimulation