A histochemically demonstrable thiaminepyrophosphatase activity in the sinusoidal endothelium of the liver

Summary A new histochemically demonstrable thiaminepyrophosphatase activity in liver tissue is described. It appears to be localized solely to the cytosomes of the sinusoidal endothelium. The activity, which requires high concentration of lead ion for its demonstration, has a high degree of substrate specificity. It resists formaldehyde fixation, ethanol and many inhibitors. The optimum pH is at pH 6.This study was supported in part by a grant from the Swedish Medical Research Council.     

A comparison between histochemically demonstrable Golgi-associated and bile canalicular TDP-ase activity in liver

Summary Histochemically demonstrable Golgi-associated TDP-ase activity in liver cells from cat, chicken, rat and frog has been investigated.This activity is highly substrate-specific, insensitive to aldehyde fixation, ethanol, acetate, lead and most enzyme inhibitors. It is stimulated by divalent manganese, calcium, magnesium and cobalt and optimum pH is at pH 6 to 7.The characteristics are identical for all four species but significant differences exist at a comparison with bile canalicular activity, Golgi-associated activity in other cells and biochemical findings.This study was supported in part by a grant from the Swedish Medical Research Council.