Literature DB >> 3213627

Adenine, guanine, and inosine nucleotides of chick growth cartilage: relationship between energy status and the mineralization process.

H Matsumoto1, K DeBolt, I M Shapiro.   

Abstract

The major aim of this investigation was to measure the nucleotide content of the developing chick epiphysis and to relate changes in nucleotide levels to chondrocyte maturation and the development of mineralization. Using a cryostat, sections of cartilage were isolated from the proximal head of the tibial growth cartilage, care being taken to preserve the metabolic integrity of the tissue. Sections were identified microscopically, pooled, and the nucleotide and nucleoside content of each sample determined by HPLC. Procedures used for the study were shown to minimize degradation of nucleotides. Their effectiveness was assessed through an evaluation of the rapid freezing technique and by examination of the effects of apatite on the recovery of endogenous and added nucleotides. Analysis of nucleotide levels in the growth cartilage indicated that chondrocytes undergo a profound change in energy metabolism during development and maturation. Thus, in the premineralized resting and proliferative zones, ATP and, to a lesser extent, GTP values were high, suggesting that the chondrocytes obtained metabolic energy through both glycolytic and mitochondrial oxidative processes. In the hypertrophic zone and in calcified cartilage, there was a profound decrease in the ATP concentration and a corresponding fall in the energy charge and the ATP/ADP ratios. The nucleotide levels in this zone indicated that there was increased reliance on nonoxidative metabolism. Measurement of nucleoside levels in premineralized cartilage suggested that there was little resynthesis of nucleotides through the salvage pathway. These observed changes in nucleotide values are consistent with earlier observations concerning chondrocyte redox and the low pO2 tension of the hypertrophic zone.2+off

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Year:  1988        PMID: 3213627     DOI: 10.1002/jbmr.5650030315

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  6 in total

1.  Retinoic acid modulation of glutathione and cysteine metabolism in chondrocytes.

Authors:  C C Teixeira; I M Shapiro; M Hatori; R Rajpurohit; C Koch
Journal:  Biochem J       Date:  1996-02-15       Impact factor: 3.857

2.  Chondrocyte autophagy is stimulated by HIF-1 dependent AMPK activation and mTOR suppression.

Authors:  Jolene Bohensky; Serge Leshinsky; Vickram Srinivas; Irving M Shapiro
Journal:  Pediatr Nephrol       Date:  2009-10-15       Impact factor: 3.714

3.  Viable cells are a requirement for in vitro cartilage calcification.

Authors:  A L Boskey; S B Doty; D Stiner; I Binderman
Journal:  Calcif Tissue Int       Date:  1996-03       Impact factor: 4.333

Review 4.  The Role of Mitochondrial Metabolism, AMPK-SIRT Mediated Pathway, LncRNA and MicroRNA in Osteoarthritis.

Authors:  Hao-Yu Liu; Chi-Fen Chang; Cheng-Chang Lu; Shun-Cheng Wu; Bin Huang; Tsung-Lin Cheng; Sung-Yen Lin; Cheng-Jung Ho; Mon-Juan Lee; Chung-Da Yang; Ying-Chun Wang; Jhong-You Li; Ping-Cheng Liu; Chun-Wang Wei; Lin Kang; Chung-Hwan Chen
Journal:  Biomedicines       Date:  2022-06-22

5.  Gene expression and extracellular matrix ultrastructure of a mineralizing chondrocyte cell culture system.

Authors:  L C Gerstenfeld; W J Landis
Journal:  J Cell Biol       Date:  1991-02       Impact factor: 10.539

6.  Next-generation sequencing identifies equine cartilage and subchondral bone miRNAs and suggests their involvement in osteochondrosis physiopathology.

Authors:  Clémence Desjardin; Anne Vaiman; Xavier Mata; Rachel Legendre; Johan Laubier; Sean P Kennedy; Denis Laloe; Eric Barrey; Claire Jacques; Edmond P Cribiu; Laurent Schibler
Journal:  BMC Genomics       Date:  2014-09-17       Impact factor: 3.969

  6 in total

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