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PXD022682

PXD022682 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleLipocalin 13 enhances insulin secretion but is dispensable for systemic metabolic control
DescriptionMembers of the lipocalin protein family serve as biomarkers for kidney disease and acute phase inflammatory reactions, and are under pre-clinical development for the diagnosis and therapy of allergies. However, none of the lipocalin family members has made the step into clinical development, mostly due to their complex biological activity and the lack of in-depth mechanistic knowledge. Here, we show that the hepatokine lipocalin 13 (LCN13) triggers glucose-dependent insulin secretion and cell proliferation of primary mouse islets. However, inhibition of endogenous LCN13 expression in lean mice did not alter glucose and lipid homeostasis. Enhanced hepatic secretion of LCN13 in either diet-induced or genetic obesity led to no discernable impact on systemic energy homeostasis, neither in preventive nor therapeutic setting. Of note, loss or forced LCN13 hepatic secretion did not trigger any compensatory regulation of related lipocalin family members. Together, these data are in stark contrast to the suggested gluco-regulatory and therapeutic role of LCN13 in obesity, and imply complex regulatory steps in LCN13 biology at the organismic level mitigating its principal insulinotropic effects.
HostingRepositoryPRIDE
AnnounceDate2021-02-02
AnnouncementXMLSubmission_2021-02-02_04:28:52.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterChristine von Toerne
SpeciesList scientific name: Mus musculus (Mouse); NCBI TaxID: 10090;
ModificationListNo PTMs are included in the dataset
InstrumentQ Exactive HF
Dataset History
RevisionDatetimeStatusChangeLog Entry
02020-11-24 01:24:20ID requested
12021-02-02 04:28:53announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: Hepatokine, Lipocalin 13, Metabolic diseases, Obesity, Type 2 diabetes
Contact List
Stephan Herzig
contact affiliationInstitute for Diabetes and Cancer (IDC), Helmholtz Centre Munich, German Research Center for Environmental Health, Neuherberg, Germany
contact emailstephan.herzig@helmholtz-muenchen.de
lab head
Christine von Toerne
contact affiliationHelmholtz Zentrum München
contact emailvontoerne@helmholtz-muenchen.de
dataset submitter
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Dataset FTP location
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PRIDE project URI
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