2006
DOI: 10.1369/jhc.5a6745.2005
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In Situ Localization of Transketolase Activity in Epithelial Cells of Different Rat Tissues and Subcellularly in Liver Parenchymal Cells

Abstract: S U M M A R Y Metabolic mapping of enzyme activities (enzyme histochemistry) is an important tool to understand (patho)physiological functions of enzymes. A new enzyme histochemical method has been developed to detect transketolase activity in situ in various rat tissues and its ultrastructural localization in individual cells. In situ detection of transketolase is important because this multifunctional enzyme has been related with diseases such as cancer, diabetes, Alzheimer's disease, and Wernicke-Korsakoff'… Show more

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Cited by 22 publications
(22 citation statements)
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“…Thiamine pyrophosphatase is a trans-Golgi marker enzyme [40,42]. Recent studies indicate that the thiamine dependent enzyme transketolase is localized around the endoplasmic reticulum (ER) [4]. The ER is involved in post-translational protein processing and transport.…”
Section: Discussionmentioning
confidence: 99%
“…Thiamine pyrophosphatase is a trans-Golgi marker enzyme [40,42]. Recent studies indicate that the thiamine dependent enzyme transketolase is localized around the endoplasmic reticulum (ER) [4]. The ER is involved in post-translational protein processing and transport.…”
Section: Discussionmentioning
confidence: 99%
“…First of all, tumor cells have high rates of anaerobic glycolysis (known as the Warburg effect) and PPP activity in comparison to their nontransformed counterparts [138,139], resulting in an enrichment of reducing power in the form of NADPH and GSH. Because GSH is highly reactive and is present in relatively high concentrations (falling in the millimolar range) within cells, it is the main factor responsible for the maintenance of the cellular redox state and determines sensitivity or resistance to apoptosis induced by various stimuli [140], including anticancer drugs.…”
Section: The Ppp and Response To Chemotherapymentioning
confidence: 99%
“…Control reactions were incubated in the absence of substrate and coenzyme. 30,31 In situ determination of transketolase activity was performed according to Boren et al 32 Incubation medium contained 18% (w/ v) PVA in 50 mM Tris-HCl buffer, pH 7.6, 5 mM sodium azide, 7.5 mM NAD 1 , 3.7 mM KH 2 PO 4 , 5 mM MgCl 2 , 0.45 mM methoxyphenazine methosulphate, 100 lL substrate mixture (prepared as described above) per mL incubation medium, 0.1 mM TPP and 5 mM NBT. The medium was freshly prepared just before incubation and NBT was added after being dissolved in a heated mixture of DMF and ethanol (1:1) (final dilution of each solvent in the medium was 2% v/v).…”
Section: Cell Sortingmentioning
confidence: 99%