TY - JOUR
T1 - Secreted Metabolome of Human Macrophages Exposed to Methamphetamine
AU - Pawlak, Katarzyna
AU - Lech, Katarzyna
AU - Vei, Akou
AU - Burch, Sydney
AU - Zieschang, Sarah
AU - Jaquet, Spencer
AU - Yu, Fang
AU - Harwood, Emma
AU - Morsey, Brenda
AU - Fox, Howard S.
AU - Ciborowski, Pawel
N1 - Funding Information:
The authors would like to thank Dr. Michael Belshan (Creighton University; Omaha, NE) for his critical review of this manuscript and Robin Taylor for editorial assistance. Financial support was provided by National Institutes of Health Grants: R01 DA043258 and P30 MH062261.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/6/20
Y1 - 2019/6/20
N2 - Macrophages comprise a major component of the human innate immune system that is involved in maintaining homeostasis and responding to infections or other insults. Besides cytokines and chemokines, macrophages presumably influence the surrounding environment by secreting various types of metabolites. Characterization of secreted metabolites under normal and pathological conditions is critical for understanding the complex innate immune system. To investigate the secreted metabolome, we developed a novel workflow consisting of one Reverse Phase (RP) C18 column linked in tandem with a Cogent cholesterol-modified RP C18. This system was used to compare the secreted metabolomes of human monocyte-derived macrophages (hMDM) under normal conditions to those exposed to methamphetamine (Meth). This new experimental approach allowed us to measure 92 metabolites, identify 11 of them as differentially expressed, separate and identify three hydroxymethamphetamine (OHMA) isomers, and identify a new, yet unknown metabolite with a m/z of 192. This study is the first of its kind to address the secreted metabolomic response of hMDM to an insult by Meth. Besides the discovery of novel metabolites secreted by macrophages, we provide a novel methodology to investigate metabolomic profiling.
AB - Macrophages comprise a major component of the human innate immune system that is involved in maintaining homeostasis and responding to infections or other insults. Besides cytokines and chemokines, macrophages presumably influence the surrounding environment by secreting various types of metabolites. Characterization of secreted metabolites under normal and pathological conditions is critical for understanding the complex innate immune system. To investigate the secreted metabolome, we developed a novel workflow consisting of one Reverse Phase (RP) C18 column linked in tandem with a Cogent cholesterol-modified RP C18. This system was used to compare the secreted metabolomes of human monocyte-derived macrophages (hMDM) under normal conditions to those exposed to methamphetamine (Meth). This new experimental approach allowed us to measure 92 metabolites, identify 11 of them as differentially expressed, separate and identify three hydroxymethamphetamine (OHMA) isomers, and identify a new, yet unknown metabolite with a m/z of 192. This study is the first of its kind to address the secreted metabolomic response of hMDM to an insult by Meth. Besides the discovery of novel metabolites secreted by macrophages, we provide a novel methodology to investigate metabolomic profiling.
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U2 - 10.1021/acs.analchem.9b01952
DO - 10.1021/acs.analchem.9b01952
M3 - Article
C2 - 31265257
AN - SCOPUS:85069948710
SN - 0003-2700
VL - 91
SP - 9190
EP - 9197
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 14
ER -