Summary of Study ST003389
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 PR002100. The data can be accessed directly via it's Project DOI: 10.21228/M85J80 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.
Study ID | ST003389 |
Study Title | Disruption of Glucose Homeostasis by Bacterial Infection Orchestrates Host Innate Immunity Through NAD+/NADH Balance |
Study Summary | Metabolic reprogramming is crucial for activating innate immunity in macrophages, and the accumulation of immunometabolites is thought essential for effective defense against infection. The NAD+/NADH redox couple serves as a critical node that integrates metabolic pathways and signaling events, but how this metabolite couple engages macrophage activation remains unclear. Here, we showed that the NAD+/NADH ratio serves as a molecular signal that regulates proinflammatory responses and type I interferon (IFN) responses divergently. Salmonella Typhimurium infection led to a decreased NAD+/NADH ratio by inducing the accumulation of NADH. Further investigation showed that an increased NAD+/NADH ratio correlates to attenuated proinflammatory responses and enhanced type I IFN responses. Conversely, a decreased NAD+/NADH ratio is linked to intensified proinflammatory responses and restrained type I IFN responses. These results showed the NAD+/NADH ratio is an essential cell-intrinsic factor that orchestrates innate immunity, which enhanced our understanding of how metabolites fine-tune innate immunity. |
Institute | Northwest A&F University |
Last Name | Xu |
First Name | Lei |
Address | Yangling, Xinong Road, Xiyang, 712100, China |
xulei@nwafu.edu.cn | |
Phone | 18149321513 |
Submit Date | 2024-07-27 |
Raw Data Available | Yes |
Raw Data File Type(s) | mzML |
Analysis Type Detail | LC-MS |
Release Date | 2024-08-09 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR002100 |
Project DOI: | doi: 10.21228/M85J80 |
Project Title: | The metabolome analysis of energy metabolites after Salmonella Typhimurium infection in mouse macrophages |
Project Type: | The metabolome analysis of energy metabolites |
Project Summary: | The metabolome analysis of energy metabolites after Salmonella Typhimurium infection in mouse macrophages. Glucose metabolites concentrations in S. Typhimurium-infected (MOI = 10, 6 h) and Mock-infected mouse Peritoneal macrophages (PM). PMs were also pretreated with 2-DG (10 mM, 18 h) and infected with S. Typhimurium (MOI =10, 6 h) or Mock-infected. PMs were also pretreated with Rotenone (2.5 μM, 4 h) and infected with S. Typhimurium (MOI =10, 6 h) or Mock-infected. |
Institute: | Northwest A&F University |
Last Name: | Xu |
First Name: | Lei |
Address: | Yangling, Xinong Road, Xianyang, 712100, China |
Email: | xulei@nwafu.edu.cn |
Phone: | 18149321513 |
Subject:
Subject ID: | SU003511 |
Subject Type: | Mammal |
Subject Species: | Mus musculus |
Taxonomy ID: | 10090 |
Subject ID: | SU003512 |
Subject Type: | Mammal |
Subject Species: | Mus musculus |
Taxonomy ID: | 10090 |
Factors:
Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)
mb_sample_id | local_sample_id | Sample source | Factor |
---|---|---|---|
SA367989 | STPM7 | Peritoneal macrophages | 2DG+Salmonella Typhimurium infection1 |
SA368001 | STPM7 | Peritoneal macrophages | 2DG+Salmonella Typhimurium infection1 |
SA367990 | STPM8 | Peritoneal macrophages | 2DG+Salmonella Typhimurium infection2 |
SA368002 | STPM8 | Peritoneal macrophages | 2DG+Salmonella Typhimurium infection2 |
SA367991 | STPM9 | Peritoneal macrophages | 2DG+Salmonella Typhimurium infection3 |
SA368003 | STPM9 | Peritoneal macrophages | 2DG+Salmonella Typhimurium infection3 |
SA367992 | STPM1 | Peritoneal macrophages | Control1 |
SA368004 | STPM1 | Peritoneal macrophages | Control1 |
SA367993 | STPM2 | Peritoneal macrophages | Control2 |
SA368005 | STPM2 | Peritoneal macrophages | Control2 |
SA367994 | STPM3 | Peritoneal macrophages | Control3 |
SA368006 | STPM3 | Peritoneal macrophages | Control3 |
SA367995 | STPM10 | Peritoneal macrophages | Rotenone+Salmonella Typhimurium infection1 |
SA368007 | STPM10 | Peritoneal macrophages | Rotenone+Salmonella Typhimurium infection1 |
SA367996 | STPM11 | Peritoneal macrophages | Rotenone+Salmonella Typhimurium infection2 |
SA368008 | STPM11 | Peritoneal macrophages | Rotenone+Salmonella Typhimurium infection2 |
SA367997 | STPM12 | Peritoneal macrophages | Rotenone+Salmonella Typhimurium infection3 |
SA368009 | STPM12 | Peritoneal macrophages | Rotenone+Salmonella Typhimurium infection3 |
SA367998 | STPM4 | Peritoneal macrophages | Salmonella Typhimurium infection1 |
SA368010 | STPM4 | Peritoneal macrophages | Salmonella Typhimurium infection1 |
SA367999 | STPM5 | Peritoneal macrophages | Salmonella Typhimurium infection2 |
SA368011 | STPM5 | Peritoneal macrophages | Salmonella Typhimurium infection2 |
SA368000 | STPM6 | Peritoneal macrophages | Salmonella Typhimurium infection3 |
SA368012 | STPM6 | Peritoneal macrophages | Salmonella Typhimurium infection3 |
Showing results 1 to 24 of 24 |
Collection:
Collection ID: | CO003504 |
Collection Summary: | Cells in plates were counted, washed with cold PBS and then flash-frozen in liquid nitrogen |
Sample Type: | Macrophages |
Collection ID: | CO003505 |
Collection Summary: | Cells in plates were counted, washed with cold PBS and then flash-frozen in liquid nitrogen |
Sample Type: | Macrophages |
Treatment:
Treatment ID: | TR003520 |
Treatment Summary: | The metabolome analysis of energy metabolites after Salmonella Typhimurium infection in mouse macrophages. Glucose metabolites concentrations in S. Typhimurium-infected (MOI = 10, 6 h) and Mock-infected mouse Peritoneal macrophages. PMs were also pretreated with 2-DG (10 mM, 18 h) and infected with S. Typhimurium (MOI =10, 6 h) or Mock-infected. PMs were also pretreated with Rotenone (2.5 μM, 4 h) and infected with S. Typhimurium (MOI =10, 6 h) or Mock-infected. |
Treatment ID: | TR003521 |
Treatment Summary: | The metabolome analysis of energy metabolites after Salmonella Typhimurium infection in mouse macrophages. Glucose metabolites concentrations in S. Typhimurium-infected (MOI = 10, 6 h) and Mock-infected mouse Peritoneal macrophages. PMs were also pretreated with 2-DG (10 mM, 18 h) and infected with S. Typhimurium (MOI =10, 6 h) or Mock-infected. PMs were also pretreated with Rotenone (2.5 μM, 4 h) and infected with S. Typhimurium (MOI =10, 6 h) or Mock-infected. |
Sample Preparation:
Sampleprep ID: | SP003518 |
Sampleprep Summary: | 2 × 107 cells were harvested and thawed at 4°C mixed with 200 μL water, and 800 μL of cold methanol/acetonitrile (1:1, v/v) to remove the protein. The mixture was centrifuged for 15 min (14000 × g, 4°C). The supernatant was dried in a vacuum centrifuge. |
Sampleprep ID: | SP003519 |
Sampleprep Summary: | 2 × 107 cells were harvested and thawed at 4°C mixed with 200 μL water, and 800 μL of cold methanol/acetonitrile (1:1, v/v) to remove the protein. The mixture was centrifuged for 15 min (14000 × g, 4°C). The supernatant was dried in a vacuum centrifuge. |
Combined analysis:
Analysis ID | AN005557 | AN005558 |
---|---|---|
Analysis type | MS | MS |
Chromatography type | HILIC | HILIC |
Chromatography system | Agilent 1290 Infinity | Agilent 1290 Infinity |
Column | Waters ACQUITY UPLC BEH Amide (150 x 2.1mm,1.7um) | Waters ACQUITY UPLC BEH Amide (150 x 2.1mm,1.7um) |
MS Type | ESI | ESI |
MS instrument type | Triple quadrupole | Triple quadrupole |
MS instrument name | ABI Sciex 5500 QTrap | ABI Sciex 5500 QTrap |
Ion Mode | NEGATIVE | NEGATIVE |
Units | μmol/g | umol/g |
Chromatography:
Chromatography ID: | CH004221 |
Instrument Name: | Agilent 1290 Infinity |
Column Name: | Waters ACQUITY UPLC BEH Amide (150 x 2.1mm,1.7um) |
Column Temperature: | 35°C |
Flow Gradient: | 0-18 min: 90% B to 40% B, 18-18.1 min: 40% B to 90% B, 18.1-23 min: 90% B. |
Flow Rate: | 300 μL/min |
Solvent A: | 100% water; 15 mM ammonium acetate |
Solvent B: | 100% acetonitrile |
Chromatography Type: | HILIC |
Chromatography ID: | CH004222 |
Instrument Name: | Agilent 1290 Infinity |
Column Name: | Waters ACQUITY UPLC BEH Amide (150 x 2.1mm,1.7um) |
Column Temperature: | 35°C |
Flow Gradient: | 0-18 min: 90% B to 40% B, 18-18.1 min: 40% B to 90% B, 18.1-23 min: 90% B. |
Flow Rate: | 300 μL/min |
Solvent A: | 100% water; 15 mM ammonium acetate |
Solvent B: | 100% acetonitrile |
Chromatography Type: | HILIC |
MS:
MS ID: | MS005282 |
Analysis ID: | AN005557 |
Instrument Name: | ABI Sciex 5500 QTrap |
Instrument Type: | Triple quadrupole |
MS Type: | ESI |
MS Comments: | sheath gas temperature: 350°C; ion Source Gas1 (Gas1): 45 psi, Ion Source Gas2 (Gas2): 45 psi, Curtain gas (CUR): 30 psi; IonSpray Voltage Floating (ISVF): 4500 V; nebulizer pressure: 40psi. The mass spectrometer operated with a dwell time of 200 ms. |
Ion Mode: | NEGATIVE |
MS ID: | MS005283 |
Analysis ID: | AN005558 |
Instrument Name: | ABI Sciex 5500 QTrap |
Instrument Type: | Triple quadrupole |
MS Type: | ESI |
MS Comments: | sheath gas temperature: 350°C; ion Source Gas1 (Gas1): 45 psi, Ion Source Gas2 (Gas2): 45 psi, Curtain gas (CUR): 30 psi; IonSpray Voltage Floating (ISVF): 4500 V; nebulizer pressure: 40psi. The mass spectrometer operated with a dwell time of 200 ms. |
Ion Mode: | NEGATIVE |