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Type of publication: Journal Article
Type of document: Full Paper

Year: 2014

Authors: Rupprecht, A; Sittner, D; Smorodchenko, A; Hilse, KE; Goyn, J; Moldzio, R; Seiler, AE; Bräuer, AU; Pohl, EE

Title: Uncoupling protein 2 and 4 expression pattern during stem cell differentiation provides new insight into their putative function.

Source: PLoS One. 2014; 9(2):e88474

Authors Vetmeduni Vienna:

Hilse-Koller Karolina
Moldzio Rudolf
Pohl Elena
Rupprecht Anne
Smorodchenko Alina

Vetmed Research Units
Institute for Medical Biochemistry
Institute of Physiology, Pathohysiology and Biophysics, Unit of Physiology and Biophysics

Project(s): Mechanisms of uncoupling protein activation by reactives aldehydes

Apart from the first family member, uncoupling protein 1 (UCP1), the functions of other UCPs (UCP2-UCP5) are still unknown. In analyzing our own results and those previously published by others, we have assumed that UCP"s cellular expression pattern coincides with a specific cell metabolism and changes if the latter is altered. To verify this hypothesis, we analyzed the expression of UCP1-5 in mouse embryonic stem cells before and after their differentiation to neurons. We have shown that only UCP2 is present in undifferentiated stem cells and it disappears simultaneously with the initiation of neuronal differentiation. In contrast, UCP4 is simultaneously up-regulated together with typical neuronal marker proteins TUJ-1 and NeuN during mESC differentiation in vitro as well as during murine brain development in vivo. Notably, several tested cell lines express UCP2, but not UCP4. In line with this finding, neuroblastoma cells that display metabolic features of tumor cells express UCP2, but not UCP4. UCP2"s occurrence in cancer, immunological and stem cells indicates that UCP2 is present in cells with highly proliferative potential, which have a glycolytic type of metabolism as a common feature, whereas UCP4 is strongly associated with non-proliferative highly differentiated neuronal cells.

Keywords Pubmed: Animals
Cell Differentiation
Cell Line, Tumor
Cell Proliferation
Embryonic Stem Cells/cytology*
Gene Expression Regulation, Developmental*
Gene Expression Regulation, Neoplastic*
Ion Channels/metabolism*
Membrane Transport Proteins/metabolism*
Mice, Inbred C57BL
Mitochondrial Proteins/metabolism*

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