PXD038792 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Amino acid availability acts as a metabolic rheostat to determine the magnitude of ILC2 responses - WT ILC2 |
Description | Group 2 innate lymphoid cells (ILC2) are functionally poised, tissue-resident lymphocytes that respond rapidly to damage and infection at mucosal barrier sites. ILC2 reside within complex microenvironments where they are subject to cues from both the diet and invading pathogens – including helminths. Emerging evidence suggests ILC2 are acutely sensitive not only to canonical activating signals, but also perturbations in nutrient availability. In the context of helminth infection, we identify amino acid availability as a nutritional cue in regulating ILC2 responses. ILC2 were found to be uniquely pre-primed to import amino acids via the large neutral amino acid transporters Slc7a5 and Slc7a8. Cell-intrinsic deletion of these transporters individually impaired ILC2 expansion, while concurrent loss of both transporters markedly impaired the proliferative and cytokine producing capacity of ILC2. Moreover, amino acid determined the magnitude of ILC2 responses in part via tuning of mTOR. These findings implicate essential amino acids as a metabolic requisite for optimal ILC2 responses within mucosal barrier tissues. |
HostingRepository | PRIDE |
AnnounceDate | 2022-12-22 |
AnnouncementXML | Submission_2022-12-22_05:12:21.155.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | AndrewHowden |
SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: 10090; |
ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2022-12-12 23:20:53 | ID requested | |
⏵ 1 | 2022-12-22 05:12:21 | announced | |
2 | 2024-10-22 05:41:28 | announced | 2024-10-22: Updated project metadata. |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: ILC2, immunology |
Contact List
Dr MatthewHepworth |
contact affiliation | Lydia Becker Institute of Immunology and Inflammation | Branch Lead for Immune Tolerance Division of Infection, Immunity & Respiratory Medicine| School of Biological Sciences I Faculty of Biology, Medicine and Health| The University of Manchester |
contact email | matthew.hepworth@manchester.ac.uk |
lab head | |
AndrewHowden |
contact affiliation | University of Dundee |
contact email | a.howden@dundee.ac.uk |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/12/PXD038792 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD038792
- Label: PRIDE project
- Name: Amino acid availability acts as a metabolic rheostat to determine the magnitude of ILC2 responses - WT ILC2