Literature DB >> 2164849

Cyclic guanosine monophosphate metabolism in human amnion cells trisomic for chromosome 21.

J O Karlsson1, A Sjöstedt, J Wahlström, K L Axelsson, R G Andersson.   

Abstract

An extra copy of chromosome 21, a small chromosome or a specific segment of it, is the cause of the disorder known as Down's syndrome (DS). Genes mapped to this chromosome include superoxide dismutase-1 (SOD-1) along with other enzymes. Gene dosage effects have been shown for some of these enzymes, including SOD-1. Increased SOD-1 has been suggested to stimulate the cGMP-forming enzyme, guanylate cyclase (GC). In the present study we have used amnion cells from DS subjects and normal subjects in order to indirectly test the effects of SOD-1 on the cGMP metabolism. We have measured the cAMP and cGMP content, SOD-1 activity, GC activity and cGMP phosphodiesterase (G-PDE) activity in amnion cells from DS subjects and normal subjects, respectively. The levels of cGMP in DS amnion cells were lower than in normal cells, although the SOD-1 activity was higher in DS amnion cells. Furthermore, the GC activity and the G-PDE activity were found to be lower in the trisomic cells. Our results do not support the suggestion that SOD-1 has a stimulatory effect on the GC activity.

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Year:  1990        PMID: 2164849     DOI: 10.1159/000243211

Source DB:  PubMed          Journal:  Biol Neonate        ISSN: 0006-3126


  1 in total

1.  Loss of glutathione peroxidase 3 expression is correlated with epigenetic mechanisms in endometrial adenocarcinoma.

Authors:  Eva Falck; Sandra Karlsson; Jessica Carlsson; Gisela Helenius; Mats Karlsson; Karin Klinga-Levan
Journal:  Cancer Cell Int       Date:  2010-11-24       Impact factor: 5.722

  1 in total

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