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PXD003628

PXD003628 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleSNX27 interactome during immune synapse formation
DescriptionT lymphocyte recognition of antigenic peptides on the surface of antigen-presenting cells (APC) leads to immune synapse formation (IS). By analogy with the nervous synapse, this cell-cell communication model requires the formation of highly organized structures that delimit an active zone of membrane traffic. For T cells to connect antigen recognition with the biological response, receptors and signaling proteins must be recycled. Sorting nexin 27 (SNX27) is an endosomal protein best known for its role in recycling PDZ (PSD95, Dlg1, ZO-1)-interacting neuronal proteins via the retromer transport machinery. Alteration of this sorting pathway leads to neurodegeneration and is associated to Down syndrome, Alzheimer’s and Parkinson’s diseases. In T lymphocytes, SNX27 interacts with diacylglycerol kinase zeta (DGKz), which provides a mechanistic link between diacylglycerol metabolism and membrane trafficking. Following antigen recognition, SNX27-positive endosomes polarize to the IS and a PDZ-dependent SNX27 pool accumulates at the cell-cell contact area. To test for additional SNX27 functions, we carried out proteomic analysis of the SNX27 interactome purified from T cells in contact with APC, and identified SNX27 interaction with the retromer and with members of the WASH (Wiskott-Aldrich syndrome protein and SCAR homologue) complex. This finding indicates the conserved nature of the SNX27/WASH/retromer complex in hematopoietic cells and suggests similarity between neurological diseases and abnormal immune/inflammatory responses. We also found PDZ-dependent SNX27 cargoes, including modulators of cytoskeletal reorganization such as zona occludens-2 (ZO-2). ZO-2, a cytosolic component of epithelial cell-cell junctions, localized to the IS, and SNX27 silencing affected ZO-2 stability at the synapse. This study broadens our knowledge of SNX27 function in T lymphocytes, and suggests that pathways that delimit polarized structures in epithelial systems also participate in IS regulation.
HostingRepositoryPRIDE
AnnounceDate2017-05-11
AnnouncementXMLSubmission_2017-05-11_04:15:38.xml
DigitalObjectIdentifierhttps://dx.doi.org/10.6019/PXD003628
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterGonzalo Martínez
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListmonohydroxylated residue; acetylated residue; iodoacetamide derivatized residue
InstrumentTripleTOF 5600
Dataset History
RevisionDatetimeStatusChangeLog Entry
02016-02-15 00:45:24ID requested
12017-05-11 04:15:39announced
Publication List
Tello-Lafoz M, Mart, í, nez-Mart, í, nez G, Rodr, í, guez-Rodr, í, guez C, Albar JP, Huse M, Gharbi S, Merida I, Sorting nexin 27 interactome in T-lymphocytes identifies zona occludens-2 dynamic redistribution at the immune synapse. Traffic, 18(8):491-504(2017) [pubmed]
Keyword List
curator keyword: Biomedical
submitter keyword: SNX27, ZO-2, PDZ, immune synapse, T-lymphocyte
Contact List
Isabel Mérida
contact affiliationDept of Immunology and Oncology, Centro Nacional de Biotecnología (CNB-CSIC), Darwin 3, Campus UAM Cantoblanco, 28079 Madrid, Spain
contact emailimerida@cnb.csic.es
lab head
Gonzalo Martínez
contact affiliationDepartment of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, Madrid, Spain
contact emailgmartinez@cnb.csic.es
dataset submitter
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