Summary of Study ST004402

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.

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 IDST004402
Study TitlePolar metabolomics on intracellular media of induced pluripotent stem cells (iPSC) derived forebrain excitatory neurons generated from a FXS and CRISPR edited isogenic control.
Study SummaryTo assess whether FMRP influences metabolism during neuron maturation, we differentiated isogenic lines into forebrain excitatory neurons and profiled intracellular metabolites at weeks 1. Polar metabolites during neuron differentiation revealed that amino acids, energy/nucleotide metabolism, and neurotransmitters were adversely affected in FXS cells at this stage.
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:SU004561
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
SA521264FXS_w1_2Male Homo sapien iPSCs derived neurons FXS
SA521265FXS_w1_1Male Homo sapien iPSCs derived neurons FXS
SA521266FXS_w1_3Male Homo sapien iPSCs derived neurons FXS
SA521267FXS_w1_4Male Homo sapien iPSCs derived neurons FXS
SA521268FXS_w1_5Male Homo sapien iPSCs derived neurons FXS
SA521269iControl_w1_1Male Homo sapien iPSCs derived neurons TD
SA521270iControl_w1_2Male Homo sapien iPSCs derived neurons TD
SA521271iControl_w1_3Male Homo sapien iPSCs derived neurons TD
SA521272iControl_w1_4Male Homo sapien iPSCs derived neurons TD
SA521273iControl_w1_5Male Homo sapien iPSCs derived neurons TD
Showing results 1 to 10 of 10

Collection:

Collection ID:CO004554
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. 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 Type:Cultured cells

Treatment:

Treatment ID:TR004570
Treatment Summary:No treatment other than standard culturing conditions and genotypes.

Sample Preparation:

Sampleprep ID:SP004567
Sampleprep Summary:For extraction from cell pellets from in-vitro cultures, samples were incubated on dry ice with cold 80% methanol. The extracts were spun down and the supernatant was vacuum dried before resuspending in LC/MS grade water.

Chromatography:

Chromatography ID:CH005578
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:AN007359
Analysis Type:MS
Chromatography ID:CH005578
Num Factors:2
Num Metabolites:94
Units:Peak area
  
Analysis ID:AN007360
Analysis Type:MS
Chromatography ID:CH005578
Num Factors:2
Num Metabolites:133
Units:Peak area
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