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Electron microscopic localization of adenosine triphosphate (ATP)-hydrolyzing activity in isolated matrix vesicles and reconstituted vesicles from calf cartilage
- Source :
- Journal of Histochemistry & Cytochemistry. 31:462-470
- Publication Year :
- 1983
- Publisher :
- SAGE Publications, 1983.
-
Abstract
- The presence and distribution of adenosine triphosphatase (ATPase) activity in isolated matrix vesicles and reconstituted vesicles from fetal calf epiphyseal growth plate cartilage was studied by electron microscopic cytochemical methods to determine whether phosphatase activity would be found concentrated on the inside or the outside of matrix vesicle membranes or on both sides, and whether reconstitution of vesicles from deoxycholate-solubilized substituents would lead to the reassembly of membranes with ATPase incorporated. ATPase activity was observed on both the outer and inner surfaces of the investing membranes of isolated matrix vesicles and reconstituted vesicles. A transmembrane location of ATPase could indicate phosphate transfer across the vesicle membrane. Orthophosphate released by phosphatase activity within the protected microenvironment of the matrix vesicle could combine with membrane- or lipid-bound calcium, known to be present in vesicles, to form the first hydroxyapatite mineral during calcification.
- Subjects :
- Histology
ATPase
Phosphatase
chemistry.chemical_element
Matrix (biology)
Calcium
chemistry.chemical_compound
Calcification, Physiologic
Fetus
Animals
Freeze Fracturing
Adenosine Triphosphatases
biology
Histocytochemistry
Chemistry
Vesicle
Cell Membrane
Transmembrane protein
Cell biology
Microscopy, Electron
Cartilage
Membrane
biology.protein
Cattle
Hydroxyapatites
Anatomy
Extracellular Space
Adenosine triphosphate
Subjects
Details
- ISSN :
- 15515044 and 00221554
- Volume :
- 31
- Database :
- OpenAIRE
- Journal :
- Journal of Histochemistry & Cytochemistry
- Accession number :
- edsair.doi.dedup.....3ad269bc9ffc1e26e8585b4c8e8bfe4b
- Full Text :
- https://doi.org/10.1177/31.4.6219157