Summary of Study ST004400

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 PR002783. The data can be accessed directly via it's Project DOI: 10.21228/M8XK1H This work is supported by NIH grant, U2C- DK119886.

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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 IDST004400
Study TitleExtracellular polar metabolomics on media neural progenitor cells (NPCs) generated using dual SMAD inhibition method from FXS and CRISPR edited isogenic rescue induced pluripotent stem cells (iPSCs)
Study SummaryTo test FMRP dependence of metabolite changes, we examined NPCs generated from two independent FXS lines and their CRISPR-edited isogenic rescue counterparts and did polar metabolomics on them. LC/MS profiling of extracellular polar metabolites from the cultured media (triplicates per line) showed genotype-specific differences.
Institute
UMass Chan Medical School
Last NameUMass Chan
First NameSpinelli Lab
Address55 Lake Avenue North, Worcester, Massachusetts, 01605, USA
Emailspinellilab@gmail.com
Phone(508) 856-8989 ext. 68148
Submit Date2025-11-13
Raw Data AvailableYes
Raw Data File Type(s)mzML, raw(Thermo)
Analysis Type DetailLC-MS
Release Date2025-12-01
Release Version1
Spinelli Lab UMass Chan Spinelli Lab UMass Chan
https://dx.doi.org/10.21228/M8XK1H
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR002783
Project DOI:doi: 10.21228/M8XK1H
Project Title:Metabolic Reprogramming during Human Neuron Differentiation Indicates Glutaminase as a Key Determinant in Fragile X Syndrome
Project Summary:Metabolic homeostasis gone awry is a contributor to, if not an underlying cause of, several neurologic disorders. Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by a trinucleotide repeat expansion in FMR1 and consequent loss of the encoded protein FMRP, which results in downstream molecular, neurologic, and mitochondrial deficits that are linked to cognitive impairment. In human postmortem brain, many metabolites and solute carrier proteins are coordinately dysregulated, which also occurs during differentiation of human iPSCs into excitatory neurons. Metabolic tracing in FXS neurons demonstrates a dearth of glutamine deamidation to glutamate, which reduces anaplerosis into the TCA cycle, potentially hindering bioenergetic and biosynthetic functions of mitochondria. Mechanistically, aberrant expression of glutaminase isoforms in FXS is responsible for reduced glutaminolysis, thereby altering glutamate levels which may contribute to FXS.
Institute:UMass Chan Medical School
Last Name:UMass Chan
First Name:Richter Lab
Address:55 Lake Avenue North, Worcester, Massachusetts, 01605, USA
Email:spinellilab@gmail.com
Phone:(508) 856-8989 ext. 68148

Subject:

Subject ID:SU004559
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606
Gender:Male

Factors:

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

mb_sample_id local_sample_id Sample source Genotype
SA521240C1-2_1Male Homo sapien CRISPR rescue NPC FXS
SA521241C1-2_2Male Homo sapien CRISPR rescue NPC FXS
SA521242C1-2_3Male Homo sapien CRISPR rescue NPC FXS
SA521243FXS-SW_1Male Homo sapien CRISPR rescue NPC FXS
SA521244FXS-SW_2Male Homo sapien CRISPR rescue NPC FXS
SA521245FXS-SW_3Male Homo sapien CRISPR rescue NPC FXS
SA521246iControl_1Male Homo sapien CRISPR rescue NPC TD
SA521247iControl_2Male Homo sapien CRISPR rescue NPC TD
SA521248iControl_3Male Homo sapien CRISPR rescue NPC TD
SA521249FNPC_1Male Homo sapien CRISPR rescue NPC TD
SA521250FNPC_2Male Homo sapien CRISPR rescue NPC TD
SA521251FNPC_3Male Homo sapien CRISPR rescue NPC TD
Showing results 1 to 12 of 12

Collection:

Collection ID:CO004552
Collection Summary:iPSC lines were cultured on Matrigel coated plates in mTeSR™1 (Catalog #85850) with 10uM ROCK inhibitor (Y-27632). Neural induction was performed using the embryoid body formation protocol from StemCell technologies. Briefly cells were plated on Matrigel coated AggreWell™800 wells in STEMdiff™ Neural Induction Medium + SMADi and embryoid bodies were allowed to form for 13 days followed by Rosette selection as per manufactures instructions. The rosettes were plated on Poly-L-Ornithine (PLO)/ laminin coated plates for 3 days and then dissociated into single cells and expanded as NPCs in STEMdiff™ Neural Progenitor Medium.
Sample Type:Media

Treatment:

Treatment ID:TR004568
Treatment Summary:To generate neuron precursors, NPCs were cultured in STEMdiff™ Forebrain Neuron Differentiation media (Catalog #08600) for 3 days on PLO/laminin plates followed by replating at a density of 135,000 cells/cm2 in PLO/laminin plates in STEMdiff™ Forebrain Neuron Maturation media (Catalog #08605) with Compound E for 4 weeks.

Sample Preparation:

Sampleprep ID:SP004565
Sampleprep Summary:For media, 10ul of sample was added to 90ul of 80% methanol and vortexed for 10mins before spinning to collect the supernatant containing extracted metabolites and vacuum dried. The extract was then resuspended in LC/MS grade water.

Chromatography:

Chromatography ID:CH005576
Instrument Name:Thermo Vanquish
Column Name:Merck SeQuant ZIC-HILIC (150 x 2.1mm,5um)
Column Temperature:25
Flow Gradient:20 min, 80% - 20% B; 0.5 min, 20% - 80% B; 7.5min, 80% B
Flow Rate:0.15ml/min
Solvent A:100% water; 0.1% ammonium hydroxide; 20mM ammonium carbonate
Solvent B:100% acetonitrile
Chromatography Type:HILIC

Analysis:

Analysis ID:AN007355
Analysis Type:MS
Chromatography ID:CH005576
Num Factors:2
Num Metabolites:77
Units:Peak Area
  
Analysis ID:AN007356
Analysis Type:MS
Chromatography ID:CH005576
Num Factors:2
Num Metabolites:96
Units:Peak Area
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