BIOCHEMICAL AND CYTOCHEMICAL STUDY OF TRIMETAPHOSPHATASE ACTIVITY IN MAMMALIAN TISSUES
Trimetaphosphatase (TMPase) was biochemically and cytochemically investigated using rat and guinea pig tissues. TMPase was partially purified, and its activity was visualized and measured by the method of Doty et al. (J. Histochem. Cytochem. 25: 1381, 1977), using a dot-blot apparatus. TMPase was sa...
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Published in: | ACTA HISTOCHEMICA ET CYTOCHEMICA Vol. 25; no. 1-2; pp. 53 - 59 |
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Kyoto
JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY
1992
Japan Society of Histochemistry and Cytochemistry |
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Abstract | Trimetaphosphatase (TMPase) was biochemically and cytochemically investigated using rat and guinea pig tissues. TMPase was partially purified, and its activity was visualized and measured by the method of Doty et al. (J. Histochem. Cytochem. 25: 1381, 1977), using a dot-blot apparatus. TMPase was salted out in fractions of 60-80% ammonium sulfate. TMPase activity was observed in early protein fractions of Sephadex G-100 column. The molecular weight and pI of the partially purified TMPase were 130KD and 6.1, respectively. Electrophoretically, TMPase and acid phosphatase (ACPase) activities were observed in different bands. The present results clearly demonstrated that TMPase and ACPase are two different proteins. Cytochemically, the TMPase activity was elucidated using an improved method which employs cerium salt as capture agent, and the results were compared with those of the lead-based method. The incubation medium of the cerium-based method contained 20 mM acetate buffer, pH 3.9, 2 mM cerium chloride, 1 mM trimetaphosphate, 5% sucrose, and 0.00015% Triton X-100. The localization of the TMPase activity differed from that of ACPase in all tissues employed. TMPase activity was observed mainly in tubular structures. Using the cerium-based method, nonspecific precipitates were considerably reduced as compared with the lead-based method. |
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AbstractList | Trimetaphosphatase (TMPase) was biochemically and cytochemically investigated using rat and guinea pig tissues. TMPase was partially purified, and its activity was visualized and measured by the method of Doty et al. (J. Histochem. Cytochem. 25: 1381, 1977), using a dot-blot apparatus. TMPase was salted out in fractions of 60-80% ammonium sulfate. TMPase activity was observed in early protein fractions of Sephadex G-100 column. The molecular weight and pI of the partially purified TMPase were 130KD and 6.1, respectively. Electrophoretically, TMPase and acid phosphatase (ACPase) activities were observed in different bands. The present results clearly demonstrated that TMPase and ACPase are two different proteins. Cytochemically, the TMPase activity was elucidated using an improved method which employs cerium salt as capture agent, and the results were compared with those of the lead-based method. The incubation medium of the cerium-based method contained 20 mM acetate buffer, pH 3.9, 2 mM cerium chloride, 1 mM trimetaphosphate, 5% sucrose, and 0.00015% Triton X-100. The localization of the TMPase activity differed from that of ACPase in all tissues employed. TMPase activity was observed mainly in tubular structures. Using the cerium-based method, nonspecific precipitates were considerably reduced as compared with the lead-based method. |
Author | SEGUCHI, HARUMICHI ZHANG, SHU-XIN KOBAYASHI, TOSHIIHIRO SAZ, EVA GARCIA DEL NISHIYAMA, SHOJI OKADA, TERUHIKO |
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Keywords | Tissue Vertebrata Mammalia Enzymatic activity Trimetaphosphatase Enzyme |
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References | 8. Gomori, G.: Microscopic histochemistry: Principles and Practice. University of Chicago Press, Chicago, 1952. 22. Sasaki, T. and Grant, P.R.: Fate of annular gap junctions in the papillary cells of the enamel organ in the rat incisor. Cell Tissue Res. 246; 523-530, 1986. 6. Effinger, A. and Pavelka, M.: Colchicine-induced tubular, vesicular and cisternal organelle aggregates in absorptive cells of the small intestine of the rat. I. Morphology and phosphatase cytochemistry. Biol. Cell 52; 43-52,1984. 10. Kobayashi, T., Okada, T. and Seguchi, H.: Cerium-based cytochemical method for detection of ouabain-sensitive, potassium-dependent p-nitrophenylphosphatase activity at physiological pH. J. Histochem. Cytochem. 35; 601-611, 1987. 16. Oliver, C.: Characterization of basal lysosomes in exocrine acinar cells. J. Histochem. Cytochem. 31; 1209-1216, 1983. 1. Beaudoin, A.R., Grondin, G., Lord, A. and Pelletier, M.: β-NADPHase- and TMPase-positive “gsnake-like tubules” in the exocrine pancreas. Cytochemical and im- munocytochemical studies. J. Histochem. Cytochem. 33; 569-575, 1985. 12. Livne, E. and Oliver, C.: Internalization of cationized ferritin by isolated pancreatic acinar cells. J. Histochem. Cytochem. 34; 167-176, 1986. 23. Seguchi, H., Kobayashi, T. and Okada, T.: Demonstration of adenylate cyclase activity in stria vascularis of guinea pig cochlea (in Japanese). Equilibrium Res. Suppl. 4; 1-8, 1988. 24. Spurr, A.R.: A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res. 26; 21-43, 1969. 5. Doty, S.B., Smith, C.E., Hand, A.R. and Oliver, C.: Inorganic trimetaphosphatase as a histochemical marker for lysosomes in light and electron microscopy. J. Histochem. Cytochem. 25; 1381-1384, 1977. 11. Kornberg, A.: Tripolyphosphate of trimetaphosphate in yeast extracts. J. Biol. Chem. 218; 23-31, 1956. 15. Oliver, C.: Endocytic pathways at the lateral and basal cell surfaces of exocrine acinar cells. J. Cell Biol. 95; 154161, 1982. 13. Okada, T., Seguchi, H. and Ogawa, K.: Acid phosphatase activities in the transitional epithelium of canine urinary bladder. Acta Histochem. Cytochem. 15; 639-647, 1982. 3. Berg, G.G.: The staining of trimetaphosphatases by the chelate removal method. J. Histochem. Cytochem. 12; 341-358, 1964. 17. Petty, H.R., Hermann, W. and McConnell, H.M.: Cytochemical study of macrophage lysosomal inorganic trimetaphosphatase and acid phosphatase. J. Ultrastruct. Res. 90; 80-88, 1985. 14. Oliver, C.: Cytochemical localization of acid phosphatase and trimetaphosphatase activities in exocrine acinar cells. J. Histochem. Cytochem. 28; 78-81, 1980. 21. Sasaki, M. and Fishman, W.H.: Dual ultrastructural localization of acid phosphatase in mouse kidney tubule cell. J. Histochem. Cytochem. 21; 653-660, 1973. 19. Robinson, J.M. and Karnovsky, M.J.: Ultrastructural localization of several phosphatases with cerium. J. Histochem. Cytochem. 31; 1197-1208, 1983. 20. Robinson, J.M. and Karnovsky, M.J.: Ultrastructural localization of several phosphatases with cerium. J. Histochem. Cytochem. 31; 1197-1208, 1983. 7. Graham, R.C. and Karnovsky, H.J.: The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: Ultrastructural cytochemistry by a new technique. J. Histochem. Cytochem. 14; 291-302, 1966. 4. Chu, N.M., Janckila, A.J., Wallace, J.H. and Yam, L.T.: Assessment of a method for immunochemical detection of antigen on nitrocellulose membranes. J. Histochem. Cytochem. 37; 257-263, 1989. 18. Payer, A.F., Battle, C.L. and Peake, P.L.: Ultrastructural and cytochemical effects of trypan blue on TSH stimulation of thyroid follicular cells. Cell Tissue Res. 218; 547-556, 1981. 2. Berg, G.G. and Gordon, L.H.: Presence of trimetaphosphatase in the intestinal mucosa and properties of the enzyme. J. Histochem. Cytochem. 8; 85-91, 1960. 9. Huet, J., Sentenac, A. and Fromageot, P.: Spot-immunodetection of conserved determinants in eukaryotic RNA polymerase. J. Biol. Chem. 257; 2613-2618, 1982. |
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Title | BIOCHEMICAL AND CYTOCHEMICAL STUDY OF TRIMETAPHOSPHATASE ACTIVITY IN MAMMALIAN TISSUES |
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