Literature DB >> 2530199

Intracellular distribution of Ca2+-Mg2+ adenosine triphosphatase (ATPase) in various tissues.

S Mughal1, A Cuschieri, A A al-Bader.   

Abstract

The cytochemical distribution of Ca2+-Mg2+-ATPase was studied ultrastructurally, using a lead capture method at pH 8.5 and compared in various tissues. In thymic, splenic and activated peripheral blood lymphocytes and in cultured HeLa cells activity was consistently localised on the nuclear envelope, endoplasmic reticulum, Golgi apparatus, mitochondria and weakly on centrioles, but not on the plasma membrane. Intracellular activity was similarly distributed in intestinal absorptive cells where activity was particularly strong in the Golgi apparatus, and in hepatocytes where, however, activity was generally weak. Intracellular activity was lacking in renal glomerular and tubular cells and in cerebellar neurons and neuroglia. Variable activity was present on the outer surface of the plasma membrane, particularly on the brush borders of intestinal and renal tubular absorptive cells, the basolateral invaginations of distal tubules and the bile canaliculi. Mitochondrial activity, when present, was inhibited by oligomycin. The localisation at different sites may represent biochemically different ATPases including endoplasmic reticular ATPase involved in intracellular calcium regulation, oligomycin-sensitive mitochondrial ATPase, dynein-like ATPase associated with centrioles and an ectoenzyme associated with cell surface specialisations.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2530199      PMCID: PMC1256440     

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  54 in total

1.  ELECTRON MICROSCOPIC DEMONSTRATION OF ADENOSINETRIPHOSPHATASE IN MYOFIBRILS AND SARCOPLASMIC MEMBRANES OF CARDIAC MUSCLE OF NORMAL AND ABNORMAL DOGS.

Authors:  J R SOMMER; M S SPACH
Journal:  Am J Pathol       Date:  1964-03       Impact factor: 4.307

2.  The specificity of the histochemical method for adenosine triphosphatase.

Authors:  H A PADYKULA; E HERMAN
Journal:  J Histochem Cytochem       Date:  1955-05       Impact factor: 2.479

3.  Histochemical demonstration of (Na+-K+)-activated adenosine triphosphatase.

Authors:  L Guth; R W Albers
Journal:  J Histochem Cytochem       Date:  1974-05       Impact factor: 2.479

4.  A cytochemical study of the calcium-activated adenosinetriphosphatase in hamster adrenal medulla: its occurrence in the Golgi region of chromaffin cells.

Authors:  I Benedeczky; A D Smith; F Dubois
Journal:  Histochemie       Date:  1972

5.  Three "myosin adenosine triphosphatase" systems: the nature of their pH lability and sulfhydryl dependence.

Authors:  M H Brooke; K K Kaiser
Journal:  J Histochem Cytochem       Date:  1970-09       Impact factor: 2.479

6.  Procedure for the histochemical demonstration of actomyosin ATPase.

Authors:  L Guth; F J Samaha
Journal:  Exp Neurol       Date:  1970-08       Impact factor: 5.330

7.  Evidence for a KCl-Stimulated, Mg-ATPase on the Golgi of Corn Coleoptiles.

Authors:  A Chanson; E McNaughton; L Taiz
Journal:  Plant Physiol       Date:  1984-10       Impact factor: 8.340

8.  Role of calcium ions in the regulation of intramitochondrial metabolism. Effects of Na+, Mg2+ and ruthenium red on the Ca2+-stimulated oxidation of oxoglutarate and on pyruvate dehydrogenase activity in intact rat heart mitochondria.

Authors:  R M Denton; J G McCormack; N J Edgell
Journal:  Biochem J       Date:  1980-07-15       Impact factor: 3.857

9.  Energy-dependent calcium sequestration activity in a Golgi apparatus fraction derived from lactating rat mammary glands.

Authors:  D W West
Journal:  Biochim Biophys Acta       Date:  1981-04-03

10.  The fine structural localization of adenosine triphosphatase in the small intestine, kidney, and liver of the rat.

Authors:  C T ASHWORTH; F J LUIBEL; S C STEWART
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.