Home > Publications Database > Analysis of the senescence-associated cell surfaceome reveals potential senotherapeutic targets. > print |
001 | 273937 | ||
005 | 20250120102327.0 | ||
024 | 7 | _ | |a 10.1111/acel.14312 |2 doi |
024 | 7 | _ | |a pmid:39228130 |2 pmid |
024 | 7 | _ | |a pmc:PMC11634743 |2 pmc |
024 | 7 | _ | |a 1474-9718 |2 ISSN |
024 | 7 | _ | |a 1474-9726 |2 ISSN |
024 | 7 | _ | |a 1474-9728 |2 ISSN |
024 | 7 | _ | |a altmetric:166954750 |2 altmetric |
037 | _ | _ | |a DZNE-2024-01411 |
041 | _ | _ | |a English |
082 | _ | _ | |a 610 |
100 | 1 | _ | |a Deng, Yushuang |0 P:(DE-2719)9001013 |b 0 |e First author |u dzne |
245 | _ | _ | |a Analysis of the senescence-associated cell surfaceome reveals potential senotherapeutic targets. |
260 | _ | _ | |a Oxford [u.a.] |c 2024 |b Wiley-Blackwell |
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 1734091327_31710 |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 The accumulation of senescent cells is thought to play a crucial role in aging-associated physiological decline and the pathogenesis of various age-related pathologies. Targeting senescence-associated cell surface molecules through immunotherapy emerges as a promising avenue for the selective removal of these cells. Despite its potential, a thorough characterization of senescence-specific surface proteins remains to be achieved. Our study addresses this gap by conducting an extensive analysis of the cell surface proteome, or 'surfaceome', in senescent cells, spanning various senescence induction regimes and encompassing both murine and human cell types. Utilizing quantitative mass spectrometry, we investigated enriched cell surface proteins across eight distinct models of senescence. Our results uncover significant changes in surfaceome expression profiles during senescence, highlighting extensive modifications in cell mechanics and extracellular matrix remodeling. Our research also reveals substantive heterogeneity of senescence, predominantly influenced by cell type and senescence inducer. A key discovery of our study is the identification of four unique cell surface proteins with extracellular epitopes. These proteins are expressed in senescent cells, absent or present at low levels in their proliferating counterparts, and notably upregulated in tissues from aged mice and an Alzheimer's disease mouse model. These proteins stand out as promising candidates for senotherapeutic targeting, offering potential pathways for the detection and strategic targeting of senescent cell populations in aging and age-related diseases. |
536 | _ | _ | |a 352 - Disease Mechanisms (POF4-352) |0 G:(DE-HGF)POF4-352 |c POF4-352 |f POF IV |x 0 |
536 | _ | _ | |a 351 - Brain Function (POF4-351) |0 G:(DE-HGF)POF4-351 |c POF4-351 |f POF IV |x 1 |
588 | _ | _ | |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de |
650 | _ | 7 | |a aging |2 Other |
650 | _ | 7 | |a cell surface proteins |2 Other |
650 | _ | 7 | |a cellular senescence |2 Other |
650 | _ | 7 | |a mass spectrometry |2 Other |
650 | _ | 7 | |a senotherapeutics |2 Other |
650 | _ | 7 | |a Senotherapeutics |2 NLM Chemicals |
650 | _ | 7 | |a Membrane Proteins |2 NLM Chemicals |
650 | _ | 2 | |a Cellular Senescence: drug effects |2 MeSH |
650 | _ | 2 | |a Animals |2 MeSH |
650 | _ | 2 | |a Humans |2 MeSH |
650 | _ | 2 | |a Mice |2 MeSH |
650 | _ | 2 | |a Senotherapeutics: pharmacology |2 MeSH |
650 | _ | 2 | |a Aging: metabolism |2 MeSH |
650 | _ | 2 | |a Membrane Proteins: metabolism |2 MeSH |
700 | 1 | _ | |a Liu, Ting |0 P:(DE-2719)9002571 |b 1 |u dzne |
700 | 1 | _ | |a Scifo, Enzo |0 P:(DE-2719)2812562 |b 2 |u dzne |
700 | 1 | _ | |a Li, Tao |b 3 |
700 | 1 | _ | |a Xie, Kan |0 P:(DE-2719)2810906 |b 4 |u dzne |
700 | 1 | _ | |a Taschler, Bernd |0 P:(DE-2719)2812256 |b 5 |u dzne |
700 | 1 | _ | |a Morsy, Sarah |0 P:(DE-2719)9002881 |b 6 |u dzne |
700 | 1 | _ | |a Schaaf, Kristina |0 P:(DE-2719)2812495 |b 7 |u dzne |
700 | 1 | _ | |a Ehninger, Armin |b 8 |
700 | 1 | _ | |a Bano, Daniele |0 P:(DE-2719)2158358 |b 9 |u dzne |
700 | 1 | _ | |a Ehninger, Dan |0 P:(DE-2719)2289209 |b 10 |e Last author |
773 | _ | _ | |a 10.1111/acel.14312 |g Vol. 23, no. 12, p. e14312 |0 PERI:(DE-600)2099130-7 |n 12 |p e14312 |t Aging cell |v 23 |y 2024 |x 1474-9718 |
856 | 4 | _ | |y OpenAccess |u https://pub.dzne.de/record/273937/files/DZNE-2024-01411.pdf |
856 | 4 | _ | |y OpenAccess |x pdfa |u https://pub.dzne.de/record/273937/files/DZNE-2024-01411.pdf?subformat=pdfa |
909 | C | O | |o oai:pub.dzne.de:273937 |p openaire |p open_access |p VDB |p driver |p dnbdelivery |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 0 |6 P:(DE-2719)9001013 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 1 |6 P:(DE-2719)9002571 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 2 |6 P:(DE-2719)2812562 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 4 |6 P:(DE-2719)2810906 |
910 | 1 | _ | |a External Institute |0 I:(DE-HGF)0 |k Extern |b 5 |6 P:(DE-2719)2812256 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 6 |6 P:(DE-2719)9002881 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 7 |6 P:(DE-2719)2812495 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 9 |6 P:(DE-2719)2158358 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 10 |6 P:(DE-2719)2289209 |
913 | 1 | _ | |a DE-HGF |b Gesundheit |l Neurodegenerative Diseases |1 G:(DE-HGF)POF4-350 |0 G:(DE-HGF)POF4-352 |3 G:(DE-HGF)POF4 |2 G:(DE-HGF)POF4-300 |4 G:(DE-HGF)POF |v Disease Mechanisms |x 0 |
913 | 1 | _ | |a DE-HGF |b Gesundheit |l Neurodegenerative Diseases |1 G:(DE-HGF)POF4-350 |0 G:(DE-HGF)POF4-351 |3 G:(DE-HGF)POF4 |2 G:(DE-HGF)POF4-300 |4 G:(DE-HGF)POF |v Brain Function |x 1 |
914 | 1 | _ | |y 2024 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0200 |2 StatID |b SCOPUS |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0160 |2 StatID |b Essential Science Indicators |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1050 |2 StatID |b BIOSIS Previews |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1190 |2 StatID |b Biological Abstracts |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0600 |2 StatID |b Ebsco Academic Search |d 2023-08-29 |
915 | _ | _ | |a JCR |0 StatID:(DE-HGF)0100 |2 StatID |b AGING CELL : 2022 |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0501 |2 StatID |b DOAJ Seal |d 2022-12-27T13:17:21Z |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0500 |2 StatID |b DOAJ |d 2022-12-27T13:17:21Z |
915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0113 |2 StatID |b Science Citation Index Expanded |d 2023-08-29 |
915 | _ | _ | |a Fees |0 StatID:(DE-HGF)0700 |2 StatID |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0150 |2 StatID |b Web of Science Core Collection |d 2023-08-29 |
915 | _ | _ | |a Creative Commons Attribution CC BY 4.0 |0 LIC:(DE-HGF)CCBY4 |2 HGFVOC |
915 | _ | _ | |a OpenAccess |0 StatID:(DE-HGF)0510 |2 StatID |
915 | _ | _ | |a Peer Review |0 StatID:(DE-HGF)0030 |2 StatID |b ASC |d 2023-08-29 |
915 | _ | _ | |a Article Processing Charges |0 StatID:(DE-HGF)0561 |2 StatID |d 2023-08-29 |
915 | _ | _ | |a IF >= 5 |0 StatID:(DE-HGF)9905 |2 StatID |b AGING CELL : 2022 |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0300 |2 StatID |b Medline |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0320 |2 StatID |b PubMed Central |d 2023-08-29 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0199 |2 StatID |b Clarivate Analytics Master Journal List |d 2023-08-29 |
920 | 1 | _ | |0 I:(DE-2719)1013005 |k AG Ehninger |l Translational Biogerontology |x 0 |
920 | 1 | _ | |0 I:(DE-2719)1013003 |k AG Bano |l Aging and Neurodegeneration |x 1 |
980 | _ | _ | |a journal |
980 | _ | _ | |a VDB |
980 | _ | _ | |a UNRESTRICTED |
980 | _ | _ | |a I:(DE-2719)1013005 |
980 | _ | _ | |a I:(DE-2719)1013003 |
980 | 1 | _ | |a FullTexts |
Library | Collection | CLSMajor | CLSMinor | Language | Author |
---|