Literature DB >> 1887819

Superoxide dismutase and catalase activities in the growth cartilage: relationship between oxidoreductase activity and chondrocyte maturation.

H Matsumoto1, S F Silverton, K Debolt, I M Shapiro.   

Abstract

Superoxide dismutase (SOD) and catalase are enzymes that protect cells from radical attack. Catalase disproportionates hydrogen peroxide, and SOD is an oxidoreductase that serves to dismutate the superoxide anion. The objective of this communication was to measure the activity of these disproportionating enzymes in the chick tibial growth cartilage and to relate enzyme activity to chondrocyte maturation and tissue calcification. Analytic techniques were optimized for the measurement of both enzymes; particular care was taken to ensure that the values obtained were due to SOD and catalase, not to the presence of other oxidases or contaminants. Catalase and SOD had similar profiles of activity in cartilage. For both enzymes, the highest levels of activity were observed in premineralized cartilage; as chondrocytes matured there was a progressive decrease in the activity of SOD and catalase. Comparison of chondrocyte SOD activity with nonmineralizing tissues indicated that the activity of cultured cartilage cells was low. We also measured the SOD activity of avascular chondrodystrophic cartilage and found it to be less than that of proliferating cartilage. When cartilage was electrofocused, three SOD isozymes were detected. The pI of the major isozyme corresponded to the copper-zinc isoform. We suggest that the observed changes in enzymatic activity are dependent on a number of cartilage-specific factors that include the vascular supply, the local production of oxygen radicals by chondrocytes, and the oxidative state of the tissue.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1887819     DOI: 10.1002/jbmr.5650060607

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


  7 in total

1.  Calcium involvement in free radical effects.

Authors:  R Bracci
Journal:  Calcif Tissue Int       Date:  1992-12       Impact factor: 4.333

2.  Vitamin E stimulates trabecular bone formation and alters epiphyseal cartilage morphometry.

Authors:  H Xu; B A Watkins; M F Seifert
Journal:  Calcif Tissue Int       Date:  1995-10       Impact factor: 4.333

3.  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

4.  Mapping the Secretome of Dental Pulp Stem Cells Under Variable Microenvironmental Conditions.

Authors:  M Bousnaki; A Bakopoulou; A Pich; E Papachristou; A Kritis; P Koidis
Journal:  Stem Cell Rev Rep       Date:  2021-09-22       Impact factor: 6.692

5.  Bioreactor-Controlled Physoxia Regulates TGF-β Signaling to Alter Extracellular Matrix Synthesis by Human Chondrocytes.

Authors:  Holger Jahr; Seval Gunes; Annika-Ricarda Kuhn; Sven Nebelung; Thomas Pufe
Journal:  Int J Mol Sci       Date:  2019-04-06       Impact factor: 5.923

6.  Reactive oxygen species induce chondrocyte hypertrophy in endochondral ossification.

Authors:  Kozo Morita; Takeshi Miyamoto; Nobuyuki Fujita; Yoshiaki Kubota; Keisuke Ito; Keiyo Takubo; Kana Miyamoto; Ken Ninomiya; Toru Suzuki; Ryotaro Iwasaki; Mitsuru Yagi; Hironari Takaishi; Yoshiaki Toyama; Toshio Suda
Journal:  J Exp Med       Date:  2007-06-18       Impact factor: 14.307

7.  The protective effects of S14G-humanin (HNG) against streptozotocin (STZ)-induced cardiac dysfunction.

Authors:  Xiaopan Chen; Chuan Yun; Hailong Zheng; Xu Chen; Qianfei Han; Hua Pan; Yang Wang; Jianghua Zhong
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.