Proteomics

Dataset Information

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Proteomics of MSC-derived exosomes upon Plekhm1-KO


ABSTRACT: Leukemia cells instruct their surrounding bone marrow microenvironment (BMM) rendering it hospitable to leukemia cell survival. Conversely, how cells of the BMM influence leukemia progression is less well understood. Pleckstrin homology domain family M member 1 (PLEKHM1) serves as a hub between fusion and secretion of intracellular vesicles. Here, we performed label-free quantitative proteomics to investigate the exosomal cargo released by BMM-derived mesenchymal stromal cells (MSC) lacking Plekhm1 compared to wild-type cells.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Stem Cell, Bone Marrow

DISEASE(S): Acute Leukemia

SUBMITTER: Georg Tascher  

LAB HEAD: Daniela Krause

PROVIDER: PXD027041 | Pride | 2023-01-16

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
20191125_GT_CK_Exosomes_KO_1.raw Raw
20191125_GT_CK_Exosomes_KO_2.raw Raw
20191125_GT_CK_Exosomes_KO_3.raw Raw
20191125_GT_CK_Exosomes_KO_4.raw Raw
20191125_GT_CK_Exosomes_WT_1.raw Raw
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Publications


Leukemia cells reciprocally interact with their surrounding bone marrow microenvironment (BMM), rendering it hospitable to leukemia cell survival, for instance through the release of small extracellular vesicles (sEVs). In contrast, we show here that BMM deficiency of pleckstrin homology domain family M member 1 (PLEKHM1), which serves as a hub between fusion and secretion of intracellular vesicles and is important for vesicular secretion in osteoclasts, accelerates murine BCR-ABL1+ B-cell acute  ...[more]

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