Gert Lubec

Prof. Dr. Gert Lubec

Programme for Proteomics, Paracelsus Medical University, Salzburg, Austria
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Research Focus & Metrics

Academic Career Length

51Years (1976-Present)

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

Representative Publications

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1 June 2012 in Cell Metabolism
Verified
Journal Article
Open access
AHArvand Haschemi
Arvand Haschemi
PKPaul Kosma
Paul Kosma
LGLars Gille
Lars Gille
CECharles Evans
Charles Evans
CBCharles F. Burant
Charles F. Burant
OWOswald Wagner
Oswald Wagner
Immune cells are somewhat unique in that activation responses can alter quantitative phenotypes upwards of 100,000-fold. To date little is known about the metabolic adaptations necessary to mount such dramatic phenotypic shifts. Screening for novel regulators of macrophage activation, we found nonprotein kinases of glucose metabolism among the most enriched classes of candidate immune modulators. We find that one of these, the carbohydrate kinase-like protein CARKL, is rapidly downregulated in vitro and in vivo upon LPS stimulation in both mice and humans. Interestingly, CARKL catalyzes an orphan reaction in the pentose phosphate pathway, refocusing cellular metabolism to a high-redox state upon physiological or artificial downregulation. We find that CARKL-dependent metabolic reprogramming is required for proper M1- and M2-like macrophage polarization and uncover a rate-limiting requirement for appropriate glucose flux in macrophage polarization.

1 March 2003 in Brain Research
Verified
Journal Article
Closed access
KKKurt Krapfenbauer
Kurt Krapfenbauer
EEEphrem Engidawork
Ephrem Engidawork
NCNigel Cairns
Nigel Cairns
MFMichael Fountoulakis
Michael Fountoulakis
GLGert Lubec
Gert Lubec

1 March 2009 in Behavioural Brain Research
Verified
Journal Article
Closed access
SPSudarshan Shantinath Patil
Sudarshan Shantinath Patil
BSBerta Sunyer
Berta Sunyer
HHHarald Höger
Harald Höger
GLGert Lubec
Gert Lubec

29 January 1999 in Philosophical Transactions of the Royal Society B: Biological Sciences
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Journal Article
Closed access
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SMS A Macko
S A Macko
MEM H Engel
M H Engel
VAV Andrusevich
V Andrusevich
GLGert Lubec
Gert Lubec
TOT C O'Connell
T C O'Connell
RHR E Hedges
R E Hedges
Fundamental to the understanding of human history is the ability to make interpretations based on artifacts and other remains which are used to gather information about an ancient population. Sequestered in the organic matrices of these remains can be information, for example, concerning incidence of disease, genetic defects and diet. Stable isotopic compositions, especially those made on isolates of collagen from bones, have been used to help suggest principal dietary components. A significant problem in the use of collagen is its long–term stability, and the possibility of isotopic alteration during early diagenesis, or through contaminating condensation reactions. In this study, we suggest that a commonly overlooked material, human hair, may represent an ideal material to be used in addressing human diets of ancient civilizations. Through the analysis of the amino–acid composition of modern hair, as well as samples that were subjected to radiation (thus simulating ageing of the hair) and hair from humans that is up to 5200 years old, we have observed little in the way of chemical change. The principal amino acids observed in all of these samples are essentially identical in relative abundances and content. Dominating the compositions are serine, glutamic acid, threonine, glycine and leucine, respectively accounting for approximately 15%, 17%, 10%, 8% and 8% of the total hydrolysable amino acids. Even minor components (for example, alanine, valine, isoleucine) show similar constancy between the samples of different ages. This constancy clearly indicates minimal alteration of the amino–acid composition of the hair. Further, it would indicate that hair is well preserved and is amenable to isotopic analysis as a tool for distinguishing sources of nutrition. Based on this observation, we have isotopically characterized modern individuals for whom the diet has been documented. Both stable nitrogen and carbon isotope compositions were assessed, and together provide an indication of trophic status, and principal type (C 3 or C 4 ) of vegetation consumed. True vegans have nitrogen isotope compositions of about 7‰ whereas humans consuming larger amounts of meat, eggs, or milk are more enriched in the heavy nitrogen isotope. We have also analysed large cross sections of modern humans from North America and Europe to provide an indication of the variability seen in a population (the supermarket diet). There is a wide diversity in both carbon and nitrogen isotope values based at least partially on the levels of seafood, corn–fed beef and grains in the diets. Following analysis of the ancient hair, we have observed similar trends in certain ancient populations. For example, the Coptics of Egypt (1000 BP) and Chinchorro of Chile (5000–800 BP) have diets of similar diversity to those observed in the modern group but were isotopically influenced by local nutritional sources. In other ancient hair (Egyptian Late Middle Kingdom mummies, ca . 4000 BP), we have observed a much more uniform isotopic signature, indicating a more constant diet. We have also recognized a primary vegetarian component in the diet of the Neolithic Ice Man of the Oetztaler Alps (5200 BP). In certain cases, it appears that sulphur isotopes may help to further constrain dietary interpretations, owing to the good preservation and sulphur content of hair. It appears that analysis of the often–overlooked hair in archaeological sites may represent a significant new approach for understanding ancient human communities.

6 February 2009 in Brain
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Journal Article
Open access
PDF file
ABAlexandra S. Baer
Alexandra S. Baer
YSYasir Ahmed Syed
Yasir Ahmed Syed
SKSung Ung Kang
Sung Ung Kang
DMDieter Mitteregger
Dieter Mitteregger
RVRaluca Vig
Raluca Vig
MKMark R.N. Kotter
Mark R.N. Kotter
Failure of oligodendrocyte precursor cell (OPC) differentiation contributes significantly to failed myelin sheath regeneration (remyelination) in chronic demyelinating diseases. Although the reasons for this failure are not completely understood, several lines of evidence point to factors present following demyelination that specifically inhibit differentiation of cells capable of generating remyelinating oligodendrocytes. We have previously demonstrated that myelin debris generated by demyelination inhibits remyelination by inhibiting OPC differentiation and that the inhibitory effects are associated with myelin proteins. In the present study, we narrow down the spectrum of potential protein candidates by proteomic analysis of inhibitory protein fractions prepared by CM and HighQ column chromatography followed by BN/SDS/SDS–PAGE gel separation using Nano-HPLC-ESI-Q-TOF mass spectrometry. We show that the inhibitory effects on OPC differentiation mediated by myelin are regulated by Fyn-RhoA-ROCK signalling as well as by modulation of protein kinase C (PKC) signalling. We demonstrate that pharmacological or siRNA-mediated inhibition of RhoA-ROCK-II and/or PKC signalling can induce OPC differentiation in the presence of myelin. Our results, which provide a mechanistic link between myelin, a mediator of OPC differentiation inhibition associated with demyelinating pathologies and specific signalling pathways amenable to pharmacological manipulation, are therefore of significant potential value for future strategies aimed at enhancing CNS remyelination.

1 June 2005 in Journal of Chromatography A
Verified
Journal Article
Closed access
Spiros GarbisSpiros Garbis
Spiros Garbis
GLGert Lubec
Gert Lubec
MFMichael Fountoulakis
Michael Fountoulakis