Summary of Study ST002140

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 PR001355. The data can be accessed directly via it's Project DOI: 10.21228/M8K70K 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.

Perform statistical analysis  |  Show all samples  |  Show named metabolites  |  Download named metabolite data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST002140
Study TitleMitochondrial respiration in B lymphocytes is essential for humoral immunity by controlling flux of the TCA cycle
Study SummaryThe function of mitochondrial respiration during B cell fate decisions and differentiation 55 remained equivocal. This study reveals that selection for mitochondrial fitness occurs during B 56 cell activation and is essential for subsequent plasma cell differentiation. By expressing a 57 mutated mitochondrial helicase in transitional B cells, we depleted mitochondrial DNA during 58 B cell maturation, resulting in reduced oxidative phosphorylation. Although no changes in 59 follicular B cell development were evident, germinal centers, class switch recombination to 60 IgG, plasma cell maturation and humoral immunity were diminished. Defective oxidative 61 phosphorylation led to aberrant flux of the tricarboxylic acid cycle and lowered the amount of 62 saturated phosphatidic acid. Consequently, mTOR activity and BLIMP1 induction were 63 curtailed whereas HIF1 _and glycolysis were amplified. Exogenous phosphatidic acid 64 increased mTOR activity in activated B cells. Hence, mitochondrial function is required and 65 selected for in activated B cells for the successful generation of functional plasma cells.
Institute
University of Erlangen-Nürnberg
DepartmentDivision of Molecular Immunology.Universitätsklinikum Erlangen, Nikolaus Fibinger Zentrum
LaboratoryProf. Mielenz
Last NameMielenz
First NameDirk
AddressNikolaus-Fiebiger-Zentrum, Glückstraße 6, 91054 Erlangen
Emaildirk.mielenz@fau.de
Phone++49 9131 8539105
Submit Date2022-04-06
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS/MS(Dir. Inf.)
Release Date2022-05-02
Release Version1
Dirk Mielenz Dirk Mielenz
https://dx.doi.org/10.21228/M8K70K
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Factors:

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

mb_sample_id local_sample_id Genotype
SA205445B cells_DNT_GPL analysis 1-S05_DNTmutant
SA205446B cells_DNT_GPL analysis 1-S03_DNTmutant
SA2054475cDNTmutant
SA205448B cells_DNT_GPL analysis 2b-S02_DNT2mutant
SA2054496cDNTmutant
SA205450B cells_DNT_GPL analysis 2b-S04_DNT4mutant
SA205451B cells_DNT_GPL analysis 2b-S10_DNT10mutant
SA205452B cells_DNT_GPL analysis 2b-S08_DNT8mutant
SA205453B cells_DNT_GPL analysis 2b-S06_DNT6mutant
SA2054544cDNTmutant
SA205455B cells_DNT_GPL analysis 1-S01_DNTmutant
SA2054564aDNTmutant
SA2054574bDNTmutant
SA2054583aDNTmutant
SA2054593bDNTmutant
SA205460B cells_DNT_GPL analysis 2b-S05_Cre5wildtype
SA2054612bCrewildtype
SA205462B cells_DNT_GPL analysis 2b-S07_Cre7wildtype
SA2054632aCrewildtype
SA205464B cells_DNT_GPL analysis 2b-S03_Cre3wildtype
SA2054651bCrewildtype
SA205466B cells_DNT_GPL analysis 2b-S01_Cre1wildtype
SA2054671aCrewildtype
SA2054682cCrewildtype
SA205469B cells_DNT_GPL analysis 1-S02_Crewildtype
SA2054701cCrewildtype
SA205471B cells_DNT_GPL analysis 1-S06_Crewildtype
SA205472B cells_DNT_GPL analysis 1-S04_Crewildtype
SA2054733cCrewildtype
Showing results 1 to 29 of 29
  logo