Tobias Eisenberg

Dr. Tobias Eisenberg

Institute of Molecular Biosciences, University of Graz, Humboldtstrasse 50/EG, 8010 Graz, Austria
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 October 2009 in Nature Cell Biology
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Tobias EisenbergTobias Eisenberg
Tobias Eisenberg
HKHeide Knauer
Heide Knauer
ASAlexandra Schauer
Alexandra Schauer
SBSabrina Büttner
Sabrina Büttner
CRChristoph Ruckenstuhl
Christoph Ruckenstuhl
FMFrank Madeo
Frank Madeo

14 November 2016 in Nature Medicine
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Tobias EisenbergTobias Eisenberg
Tobias Eisenberg
MAMahmoud Abdellatif
Mahmoud Abdellatif
SSSabrina Schroeder
Sabrina Schroeder
UPUwe Primessnig
Uwe Primessnig
SSSlaven Stekovic
Slaven Stekovic
FMFrank Madeo
Frank Madeo

26 January 2018 in Science
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FMFrank Madeo
Frank Madeo
Tobias EisenbergTobias Eisenberg
Tobias Eisenberg
FPFederico Pietrocola
Federico Pietrocola
Guido KroemerGuido Kroemer
Guido Kroemer
Having your longevity and eating too: Although caloric restriction has clear benefits for maximizing health span and life span, it is sufficiently unpleasant that few humans stick to it. Madeo et al. review evidence that increased intake of the polyamine spermidine appears to reproduce many of the healthful effects of caloric restriction, and they explain its cellular actions, which include enhancement of autophagy and protein deacetylation. Spermidine is found in foods such as wheat germ, soybeans, nuts, and some fruits and vegetables and produced by the microbiota. Increased uptake of spermidine has protective effects against cancer, metabolic disease, heart disease, and neurodegeneration. Science , this issue p. eaan2788

1 March 2014 in Molecular Cell
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Guillermo MariñoGuillermo Mariño
Guillermo Mariño
FPFederico Pietrocola
Federico Pietrocola
Tobias EisenbergTobias Eisenberg
Tobias Eisenberg
YKYongli Kong
Yongli Kong
SMShoaib Ahmad Malik
Shoaib Ahmad Malik
Guido KroemerGuido Kroemer
Guido Kroemer

21 February 2011 in Journal of Cell Biology
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EMEugenia Morselli
Eugenia Morselli
Guillermo MariñoGuillermo Mariño
Guillermo Mariño
MBMartin V. Bennetzen
Martin V. Bennetzen
Tobias EisenbergTobias Eisenberg
Tobias Eisenberg
EMEvgenia Megalou
Evgenia Megalou
Guido KroemerGuido Kroemer
Guido Kroemer
Autophagy protects organelles, cells, and organisms against several stress conditions. Induction of autophagy by resveratrol requires the nicotinamide adenine dinucleotide–dependent deacetylase sirtuin 1 (SIRT1). In this paper, we show that the acetylase inhibitor spermidine stimulates autophagy independent of SIRT1 in human and yeast cells as well as in nematodes. Although resveratrol and spermidine ignite autophagy through distinct mechanisms, these compounds stimulate convergent pathways that culminate in concordant modifications of the acetylproteome. Both agents favor convergent deacetylation and acetylation reactions in the cytosol and in the nucleus, respectively. Both resveratrol and spermidine were able to induce autophagy in cytoplasts (enucleated cells). Moreover, a cytoplasm-restricted mutant of SIRT1 could stimulate autophagy, suggesting that cytoplasmic deacetylation reactions dictate the autophagic cascade. At doses at which neither resveratrol nor spermidine stimulated autophagy alone, these agents synergistically induced autophagy. Altogether, these data underscore the importance of an autophagy regulatory network of antagonistic deacetylases and acetylases that can be pharmacologically manipulated.

15 January 2010 in Cell Death & Differentiation
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DCDidac Carmona-Gutierrez
Didac Carmona-Gutierrez
Tobias EisenbergTobias Eisenberg
Tobias Eisenberg
SBS Büttner
S Büttner
CMC Meisinger
C Meisinger
Guido KroemerGuido Kroemer
Guido Kroemer
FMF Madeo
F Madeo