Proteomics

Dataset Information

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Impact of IRP deficiency on the proteome of Ly6G+ cells from the bone marrow in mice


ABSTRACT: The overall objective of the project is to evaluate the effects of loss of function of iron regulatory proteins (IRP1, encoded by Aco1)-1 and -2 (IRP2, encoded by Ireb2) during adult life. Mice carrying floxed Aco1 and Ireb2 alleles were crossed to a knockin strain expressing a tamoxifen-inducible CRE recombinase under the control of the Rosa26 promoter. The resulting Aco1flox/flox,Ireb2flox/flox,Rosa26+/CreERT2 mice are designated P1/2-KO; littermates lacking the CreER sequence (Aco1flox/flox,Ireb2flox/flox,Rosa26+/+) serve as reference and are designated P1/2-CTR. Adult mice were injected (i.p.) with tamoxifen on day 1 and day 3 to ablate the IRPs in the whole body, and were sacrificed on day 10 for analysis. Bone marrow cells were collected and LY6G+ cells were magnetically sorted for proteome analysis by LC-MS/MS using an Ultimate 3000 UPLC system connected to an Orbitrap Exploris 480 mass spectrometer.

INSTRUMENT(S): Orbitrap Exploris 480

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Bone Marrow

SUBMITTER: Sandro Altamura  

LAB HEAD: Bruno Galy

PROVIDER: PXD032077 | Pride | 2023-03-11

REPOSITORIES: Pride

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Publications

Iron regulatory protein (IRP)-mediated iron homeostasis is critical for neutrophil development and differentiation in the bone marrow.

Bonadonna Michael M   Altamura Sandro S   Tybl Elisabeth E   Palais Gael G   Qatato Maria M   Polycarpou-Schwarz Maria M   Schneider Martin M   Kalk Christina C   Rüdiger Wibke W   Ertl Alina A   Anstee Natasha N   Bogeska Ruzhica R   Helm Dominic D   Milsom Michael D MD   Galy Bruno B  

Science advances 20221005 40


Iron is mostly devoted to the hemoglobinization of erythrocytes for oxygen transport. However, emerging evidence points to a broader role for the metal in hematopoiesis, including the formation of the immune system. Iron availability in mammalian cells is controlled by iron-regulatory protein 1 (IRP1) and IRP2. We report that global disruption of both IRP1 and IRP2 in adult mice impairs neutrophil development and differentiation in the bone marrow, yielding immature neutrophils with abnormally h  ...[more]

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