Summary of Study ST003455

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 PR002128. The data can be accessed directly via it's Project DOI: 10.21228/M8JN72 This work is supported by NIH grant, U2C- DK119886.

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Study IDST003455
Study TitleMetabolic alterations in pulmonary artery smooth muscle cells of idiopathic pulmonary arterial hypertension (IPAH) patients.
Study SummaryHypoxia-inducible factor 1α (HIF1α) is a master regulator of biological processes in hypoxia. Yet, the mechanisms and biological consequences of aerobic HIF1α activation by intrinsic factors, particularly in normal (primary) cells, remain elusive. Here, we show that HIF1α signalling is activated in several human primary vascular cells in normoxia, and in vascular smooth muscle cells (VSMCs) of normal human lungs. Mechanistically, aerobic HIF1α activation is mediated by paracrine secretion of three branched chain α-ketoacids (BCKAs), which suppress PHD2 activity via direct inhibition and via LDHA-mediated generation of L-2-hydroxyglutarate. BCKA-mediated HIF1α signalling activation stimulated glycolytic activity and governed a phenotypic switch of pulmonary artery SMCs, which correlated with BCKA metabolic dysregulation and pathophenotypic changes in pulmonary arterial hypertension patients and male rat models. We thus identify BCKAs as novel signalling metabolites that aerobically activate HIF1α and that the BCKA-HIF1α pathway modulates VSMC function, an effect that may be relevant to pulmonary vascular pathobiology.
Institute
Peking University
DepartmentDepartment of Toxicology
Last NameXiao
First NameWusheng
Address38 Xueyuan Rd, Haidian District, Beijing, Beijing, 100191, China
Emailwxiao@bjmu.edu.cn
Phone+1-010-82801628
Submit Date2023-08-07
Analysis Type DetailMALDI-MS
Release Date2024-09-19
Release Version1
Wusheng Xiao Wusheng Xiao
https://dx.doi.org/10.21228/M8JN72
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR002128
Project DOI:doi: 10.21228/M8JN72
Project Title:Aerobic activation of hypoxia-inducible factor 1alpha in vascular cells.
Project Summary:This project aims to delineate the possible mediators of aerobic activation of HIF1alpha in normal primary cells and its biological consequences related to pulmonary vascular pathobiology.
Institute:Peking University
Department:Department of Toxicology
Laboratory:WXIAO
Last Name:Xiao
First Name:Wusheng
Address:38 Xueyuan Rd, Haidian District, Beijing, Beijing, 100191, China
Email:wxiao@bjmu.edu.cn
Phone:+1-010-82801628

Subject:

Subject ID:SU003583
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606
Gender:Male and female
Species Group:Mammals

Factors:

Subject type: Cultured cells; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA382044PASMC-d#3control
SA382045PASMC-D#4control
SA382046PASMC-D#1control
SA382047PASMC-D#2control
SA382048PASMC-D#5control
SA382039PASMC-IPAH L82IPAH
SA382040PASMC-IPAH L75IPAH
SA382041PASMC-IPAH L89IPAH
SA382042PASMC-IPAH L95IPAH
SA382043PASMC-IPAH L105IPAH
Showing results 1 to 10 of 10

Collection:

Collection ID:CO003576
Collection Summary:Intracellular metabolites were collected and stored at -80 degree before LC-MS analysis.
Sample Type:Vascular smooth muscle cells
Collection Method:-80 C precold 80% LC-MS grade methanol was used to collect cell metabolites by scraping and centrifugation
Collection Location:on dry ice
Collection Duration:1 min
Storage Conditions:-80℃
Tissue Cell Identification:Pulmonary artery smooth muscle cells (PASMC)

Treatment:

Treatment ID:TR003592
Treatment Summary:human primary pulmonary artery smooth muscle cells from idiopathic pulmonary arterial hypertension patients and normal control individuals.
Treatment:normal vs diseased
Treatment Compound:N/A
Treatment Route:N/A
Treatment Dose:N/A
Treatment Dosevolume:N/A
Treatment Doseduration:N/A
Treatment Vehicle:N/A
Cell Growth Container:75 cm flasks
Cell Growth Config:1200 rpm
Cell Growth Rate:30-40 hours
Cell Media:Complete vascular smooth muscle cell growth medium supplemented with growth factors and 5% FBS
Cell Envir Cond:37 C and 5% CO2
Cell Pct Confluence:70-80%
Cell Media Lastchanged:Every 48 hours

Sample Preparation:

Sampleprep ID:SP003590
Sampleprep Summary:PASMCs were quickly washed with two volumes of ice-cold PBS, lysed for 15 min in pre-chilled 80% liquid chromatography-mass spectrometry (LC-MS)-grade methanol, and harvested by scraping on dry ice followed by centrifugation at maximal speed for 30 min at 4°C. For medium samples, 50 μL of medium were incubated in 200 μL of pre-cooled 100% LC-MS-grade methanol for 15 min on dry ice and then centrifuged as cell samples did. The supernatants of cell and medium samples were collected and evaporated to dryness on an Integrated SpeedVac System (Thermo Fisher Scientific; Waltham, MA) at 42°C. The resulting pellets were resuspended in 50 μL of LC-MS-grade water. Twenty microliters of sample were loaded in an autosampler vial for analysis.
Processing Storage Conditions:Described in summary
Extract Storage:Described in summary

Chromatography:

Chromatography ID:CH004311
Chromatography Summary:Vanquish ultra-high performance liquid chromatography system coupled to a Q Exactive mass spectrometer
Instrument Name:Thermo Vanquish
Column Name:Merck ZIC-pHILIC(150 mm × 2.1 mm,3.5um)
Column Temperature:4
Flow Gradient:gradient (%B) was 0 min, 80%; 20 min, 20%; 20.5 min, 80%; 28 min, 80%; and 42 min
Flow Rate:100
Solvent A:100% water; 20 mM ammonium carbonate; 0.1% ammonium hydroxide
Solvent B:100% acetonitrile
Chromatography Type:HILIC

Analysis:

Analysis ID:AN005676
Analysis Type:MS
Chromatography ID:CH004311
Num Factors:2
Num Metabolites:139
Units:ion intensity
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