001     137579
005     20240229105111.0
024 7 _ |a 10.1038/s41419-018-0935-9
|2 doi
024 7 _ |a pmid:30185788
|2 pmid
024 7 _ |a pmc:PMC6125596
|2 pmc
024 7 _ |a altmetric:47931032
|2 altmetric
037 _ _ |a DKFZ-2018-01459
041 _ _ |a eng
082 _ _ |a 570
100 1 _ |a Faletti, Laura
|b 0
245 _ _ |a TNFα sensitizes hepatocytes to FasL-induced apoptosis by NFκB-mediated Fas upregulation.
260 _ _ |a London [u.a.]
|c 2018
|b Nature Publishing Group
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1659693541_13808
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Although it is well established that TNFα contributes to hepatitis, liver failure and associated hepatocarcinogenesis via the regulation of inflammation, its pro-apoptotic role in the liver has remained enigmatic. On its own, TNFα is unable to trigger apoptosis. However, when combined with the transcriptional inhibitor GaLN, it can cause hepatocyte apoptosis and liver failure in mice. Moreover, along with others, we have shown that TNFα is capable of sensitizing cells to FasL- or drug-induced cell death via c-Jun N-terminal kinase (JNK) activation and phosphorylation/activation of the BH3-only protein Bim. In this context, TNFα could exacerbate hepatocyte cell death during simultaneous inflammatory and T-cell-mediated immune responses in the liver. Here we show that TNFα sensitizes primary hepatocytes, established hepatocyte cell lines and mouse embryo fibroblasts to FasL-induced apoptosis by the transcriptional induction and higher surface expression of Fas via the NFκB pathway. Genetic deletion, diminished expression or dominant-negative inhibition of the NFκB subunit p65 resulted in lower Fas expression and inhibited TNFα-induced Fas upregulation and sensitization to FasL-induced cell death. By hydrodynamic injection of p65 shRNA into the tail vein of mice, we confirm that Fas upregulation by TNFα is also NFκB-mediated in the liver. In conclusion, TNFα sensitization of FasL-induced apoptosis in the liver proceeds via two parallel signaling pathways, activation of JNK and Bim phosphorylation and NFκB-mediated Fas upregulation.
536 _ _ |a 316 - Infections and cancer (POF3-316)
|0 G:(DE-HGF)POF3-316
|c POF3-316
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed,
700 1 _ |a Peintner, Lukas
|0 0000-0002-0445-1445
|b 1
700 1 _ |a Neumann, Simon
|b 2
700 1 _ |a Sandler, Sandra
|b 3
700 1 _ |a Grabinger, Thomas
|b 4
700 1 _ |a Mac Nelly, Sabine
|b 5
700 1 _ |a Merfort, Irmgard
|b 6
700 1 _ |a Huang, Chun-Hao
|b 7
700 1 _ |a Tschaharganeh, Darjus Felix
|0 P:(DE-He78)ceccc9aed8c6e89c00795bce1f1d83a3
|b 8
|u dkfz
700 1 _ |a Kang, Tae-Won
|0 P:(DE-He78)e9f808a3a86f002da511eb9ae11f076f
|b 9
|u dkfz
700 1 _ |a Heinzmann, Florian
|0 P:(DE-HGF)0
|b 10
700 1 _ |a D'Artista, Luana
|0 P:(DE-HGF)0
|b 11
700 1 _ |a Maurer, Ulrich
|0 0000-0002-2504-1517
|b 12
700 1 _ |a Brunner, Thomas
|b 13
700 1 _ |a Lowe, Scott
|b 14
700 1 _ |a Zender, Lars
|0 P:(DE-He78)1ba2900406378e069d32db376c7818db
|b 15
|u dkfz
700 1 _ |a Borner, Christoph
|b 16
773 _ _ |a 10.1038/s41419-018-0935-9
|g Vol. 9, no. 9, p. 909
|0 PERI:(DE-600)2541626-1
|n 9
|p 909
|t Cell death & disease
|v 9
|y 2018
|x 2041-4889
909 C O |p VDB
|o oai:inrepo02.dkfz.de:137579
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 8
|6 P:(DE-He78)ceccc9aed8c6e89c00795bce1f1d83a3
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 9
|6 P:(DE-He78)e9f808a3a86f002da511eb9ae11f076f
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 10
|6 P:(DE-HGF)0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 11
|6 P:(DE-HGF)0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 15
|6 P:(DE-He78)1ba2900406378e069d32db376c7818db
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF3-310
|0 G:(DE-HGF)POF3-316
|3 G:(DE-HGF)POF3
|2 G:(DE-HGF)POF3-300
|4 G:(DE-HGF)POF
|v Infections and cancer
|x 0
914 1 _ |y 2018
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CELL DEATH DIS : 2015
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0310
|2 StatID
|b NCBI Molecular Biology Database
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0501
|2 StatID
|b DOAJ Seal
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0500
|2 StatID
|b DOAJ
915 _ _ |a Creative Commons Attribution CC BY (No Version)
|0 LIC:(DE-HGF)CCBYNV
|2 V:(DE-HGF)
|b DOAJ
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Thomson Reuters Master Journal List
915 _ _ |a WoS
|0 StatID:(DE-HGF)0111
|2 StatID
|b Science Citation Index Expanded
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
915 _ _ |a IF >= 5
|0 StatID:(DE-HGF)9905
|2 StatID
|b CELL DEATH DIS : 2015
920 1 _ |0 I:(DE-He78)F190-20160331
|k F190
|l F190 Cell Plasticity and Epigenetic Remodeling
|x 0
920 1 _ |0 I:(DE-He78)V076-20160331
|k V076
|l Translationale Gastrointestinale Onkologie
|x 1
920 1 _ |0 I:(DE-He78)L801-20160331
|k L801
|l DKTK Tübingen
|x 2
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)F190-20160331
980 _ _ |a I:(DE-He78)V076-20160331
980 _ _ |a I:(DE-He78)L801-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21