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  Quantitative and Dynamic Catalogs of Proteins Released during Apoptotic and Necroptotic Cell Death

Tanzer, M. C., Frauenstein, A., Stafford, C. A., Phulphagar, K., Mann, M., & Meissner, F. (2020). Quantitative and Dynamic Catalogs of Proteins Released during Apoptotic and Necroptotic Cell Death. CELL REPORTS, 30(4), 1260-1270.e5. doi:10.1016/j.celrep.2019.12.079.

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 Creators:
Tanzer, Maria C.1, Author           
Frauenstein, Annika2, Author           
Stafford, Che A.3, Author
Phulphagar, Kshiti2, Author           
Mann, Matthias1, Author           
Meissner, Felix2, Author           
Affiliations:
1Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565159              
2Meissner, Felix / Experimental Systems Immunology, Max Planck Institute of Biochemistry, Max Planck Society, ou_2149678              
3external, ou_persistent22              

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Free keywords: MIXED LINEAGE KINASE; MEDIATES NECROPTOSIS; LYSOSOMAL EXOCYTOSIS; PLASMA-MEMBRANE; MLKL; ACTIVATION; NECROSIS; DOMAIN; SURFACE; CIAP1
 Abstract: The inflammatory functions of the cytokine tumor necrosis factor (TNF) rely on its ability to induce cytokine production and to induce cell death. Caspase-dependent and caspase-independent pathways-apoptosis and necroptosis, respectively-regulate immunogenicity by the release of distinct sets of cellular proteins. To obtain an unbiased, systems-level understanding of this important process, we here applied mass spectrometry-based proteomics to dissect protein release during apoptosis and necroptosis. We report hundreds of proteins released from human myeloid cells in time course experiments. Both cell death types induce receptor shedding, but only apoptotic cells released nucleosome components. Conversely, necroptotic cells release lysosomal components by activating lysosomal exocytosis at early stages of necroptosis-induced membrane permeabilization and show reduced release of conventionally secreted cytokines.

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Language(s): eng - English
 Dates: 2020
 Publication Status: Issued
 Pages: 16
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Degree: -

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Title: CELL REPORTS
Source Genre: Journal
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Publ. Info: 50 HAMPSHIRE ST, FLOOR 5, CAMBRIDGE, MA 02139 USA : CELL PRESS
Pages: - Volume / Issue: 30 (4) Sequence Number: - Start / End Page: 1260 - 1270.e5 Identifier: ISSN: 2211-1247