Summary of Study ST002378

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001524. The data can be accessed directly via it's Project DOI: 10.21228/M8Q13W This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002378
Study TitleTargeted metabolomics analysis of WT and GSDMDKO macrophages
Study TypeMS analysis
Study SummaryActivating macrophage NLRP3 inflammasome can promote excessive inflammation, with severe cell and tissue damage and organ dysfunction. Here, we show that pharmacological or genetic inhibition of pyruvate dehydrogenase kinase (PDHK) significantly attenuates NLRP3 inflammasome activation in murine and human macrophages and septic mice by lowering caspase-1 cleavage and IL-1beta secretion. Inhibiting PDHK reverses NLRP3 inflammasome-induced metabolic reprogramming, enhances autophagy, promotes mitochondrial fusion over fission, preserves cristae ultrastructure, and attenuates mitochondrial ROS production. The suppressive effect of PDHK inhibition on the NLRP3 inflammasome is independent of its canonical role as a pyruvate dehydrogenase regulator. We suggest that PDHK inhibition improves mitochondrial fitness by reversing NLRP3 inflammasome activation in acutely inflamed macrophages.
Institute
Wake Forest School of Medicine
Last NameZhu
First NameXuewei
Address575 Patterson Ave, Winston-Salem, NC 27101
Emailxwzhu@wakehealth.edu
Phone3367131445
Submit Date2022-11-16
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2022-12-15
Release Version1
Xuewei Zhu Xuewei Zhu
https://dx.doi.org/10.21228/M8Q13W
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Cultured cells; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Genotype
SA237399GSDMD-LPS-1GSDMDKO | Treatment:LPS
SA237400GSDMD-LPS-2GSDMDKO | Treatment:LPS
SA237401GSDMD-LPS-3GSDMDKO | Treatment:LPS
SA237402GSDMD-LPS-4GSDMDKO | Treatment:LPS
SA237403GSDMD-ATP-2GSDMDKO | Treatment:LPS+ATP
SA237404GSDMD-ATP-4GSDMDKO | Treatment:LPS+ATP
SA237405GSDMD-ATP-3GSDMDKO | Treatment:LPS+ATP
SA237406GSDMD-ATP-1GSDMDKO | Treatment:LPS+ATP
SA237407GSDMD-JX-1GSDMDKO | Treatment:LPS+JX06+ATP
SA237408GSDMD-JX-4GSDMDKO | Treatment:LPS+JX06+ATP
SA237409GSDMD-JX-2GSDMDKO | Treatment:LPS+JX06+ATP
SA237410GSDMD-JX-3GSDMDKO | Treatment:LPS+JX06+ATP
SA237411GSDMD-control-2GSDMDKO | Treatment:no treatment
SA237412GSDMD-control-4GSDMDKO | Treatment:no treatment
SA237413GSDMD-control-3GSDMDKO | Treatment:no treatment
SA237414GSDMD-control-1GSDMDKO | Treatment:no treatment
SA237415WT-LPS-3WT | Treatment:LPS
SA237416WT-LPS-1WT | Treatment:LPS
SA237417WT-LPS-2WT | Treatment:LPS
SA237418WT-LPS-4WT | Treatment:LPS
SA237419WT-ATP-1WT | Treatment:LPS+ATP
SA237420WT-ATP-4WT | Treatment:LPS+ATP
SA237421WT-ATP-2WT | Treatment:LPS+ATP
SA237422WT-ATP-3WT | Treatment:LPS+ATP
SA237423WT-JX-3WT | Treatment:LPS+JX06+ATP
SA237424WT-JX-4WT | Treatment:LPS+JX06+ATP
SA237425WT-JX-2WT | Treatment:LPS+JX06+ATP
SA237426WT-JX-1WT | Treatment:LPS+JX06+ATP
SA237427WT-control-2WT | Treatment:no treatment
SA237428WT-control-3WT | Treatment:no treatment
SA237429WT-control-1WT | Treatment:no treatment
SA237430WT-control-4WT | Treatment:no treatment
Showing results 1 to 32 of 32
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