Literature DB >> 357726

Ca2+ transport by chondrocyte mitochondria of the epiphyseal growth plate.

N H Lee, I M Shapiro.   

Abstract

In a study of the Ca2+ kinetics of mitochondria of chick epiphyseal chondrocytes, the rate of Ca2+ uptake was linear up to a medium Ca2+ concentration of 30 mum. The half maximal transport rate occurred at 34 mum Ca2+. The Ca2+ uptake rate, expressed as a function of time, was 35 nmoles/mg protein/min; the presence of Mg2+ had little effect on Ca2+ accumulation. While these kinetic parameters did not differ significantly from mitochondria of cells of nonmineralizing tissues, the respiratory characteristics of the chondrocyte organelles exhibited functional differences. Thus, up to 350 nmoles Ca2+/mg protein, chondrocyte mitochondria performed coupled oxidative phosphorylation. Calcium uptake was energy supported, while Ca2+ binding was low. Addition of respiratory inhibitors and uncouplers to these mitochondria resulted in a rapid loss of more than 80% of the total Ca2+. The Ca/Pi ratio of the extrudate was very similar to the ratio of the ions in cartilage septum fluid. In the most mineralized zones of the epiphyseal plate, there was little change in the state 4 respiratory rate, but nonspecific Ca2+ binding was elevated and a high percentage of the total Ca2+ was in a nonextrudable form. The results indicate that in cells preparing for mineralization, much of the total mitochondrial Ca2+ is in a form that can be transported to the calcification front. In cells close to the calcification front, nonextrudable Ca2+ may form calcium phosphate granules described by other investigators.

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Year:  1978        PMID: 357726     DOI: 10.1007/bf01871999

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  36 in total

1.  On the role of the adenosine diphosphate-adenosine triphosphate exchange reaction in oxidative phosphorylation: Effect of calcium.

Authors:  F L. Bygrave; K C. Reed
Journal:  FEBS Lett       Date:  1970-05-01       Impact factor: 4.124

2.  CALCIUM ION ACCUMULATION AND VOLUME CHANGES OF ISOLATED LIVER MITOCHONDRIA. CALCIUM ION-INDUCED SWELLING.

Authors:  J B CHAPPELL; A R CROFTS
Journal:  Biochem J       Date:  1965-05       Impact factor: 3.857

3.  Subcellular fractions of smooth muscle. Isolation, substrate utilization and Ca++ transport by main pulmonary artery and mesenteric vein mitochondria.

Authors:  J Vallières; A Scarpa; A P Somlyo
Journal:  Arch Biochem Biophys       Date:  1975-10       Impact factor: 4.013

4.  Calcium does not uncouple oxidative phosphorylation in tightly-coupled mitochondria from Ehrlich ascites tumour cells.

Authors:  R F Thorne; F L Bygrave
Journal:  Nature       Date:  1974-03-22       Impact factor: 49.962

Review 5.  Energy-linked ion movements in mitochondrial systems.

Authors:  A L Lehninger; E Carafoli; C S Rossi
Journal:  Adv Enzymol Relat Areas Mol Biol       Date:  1967

6.  Mitochondrial granules in chondrocytes, osteoblasts and osteocytes. An ultrastructural and microincineration study.

Authors:  J H Martin; J L Matthews
Journal:  Clin Orthop Relat Res       Date:  1970 Jan-Feb       Impact factor: 4.176

7.  Effects of a disulfide (Ellman's reagent) and thiols on oxidative phosphorylation and ion transport by rat liver mitochondria.

Authors:  N Haugaard; N H Lee; R Kostrzewa; E S Haugaard
Journal:  Biochem Pharmacol       Date:  1969-10       Impact factor: 5.858

8.  Alkaline phosphatase activity associated to a calcium binding glycoprotein from calf scapula cartilage.

Authors:  F Vittur; B De Bernard
Journal:  FEBS Lett       Date:  1973-12-15       Impact factor: 4.124

9.  Partition of calcium, phosphate, and protein in the fluid phase aspirated at calcifying sites in epiphyseal cartilage.

Authors:  D S Howell; J C Pita; J F Marquez; J E Madruga
Journal:  J Clin Invest       Date:  1968-05       Impact factor: 14.808

10.  Ion-induced ultrastructural transformations in isolated mitochondria. The energized uptake of calcium.

Authors:  C R Hackenbrock; A I Caplan
Journal:  J Cell Biol       Date:  1969-07       Impact factor: 10.539

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