Literature DB >> 2601414

Aging increases adenosine and inosine release by human fibroblast cultures.

M F Ethier1, R B Hickler, J G Dobson.   

Abstract

The effect of in vitro age and donor age on net release of adenosine and inosine was studied in cultures of normal human fibroblasts. Confluent cultures of low-(population doubling level [PDL] 23-25) and high- (PDL 43-45) passage human lung fibroblasts derived from a 16-week-old fetal donor (IMR-90) were incubated for 30 min in physiological saline and the release of adenosine and inosine into the saline was determined by HPLC. Release of adenosine and inosine into the saline bathing low-passage human skin fibroblasts derived from a 16-week-old fetal donor (GM6111) was also determined and compared with two strains of low-passage skin fibroblasts from aged (66-67 years) donors (GM3529 and GM3524). The release of adenosine and inosine by low-passage cultures of fetal lung fibroblasts was 911 and 225 pmol/30 min per mg protein, respectively. In high-passage cultures of lung fibroblasts, release of adenosine and inosine was significantly greater at 1403 and 351 pmol/30 min per mg protein, respectively. The release of adenosine and inosine by low-passage cultures of fetal skin fibroblasts was 250 and 179 pmol/30 min per mg protein, respectively. In low-passage skin fibroblasts from aged donors, release of adenosine and inosine was significantly greater at 583 and 652 pmol/30 min per mg protein, respectively. These results indicate that the net release of adenosine and inosine by cultured human fibroblasts into their extracellular environment is enhanced by in vitro aging of lung fibroblasts and is greater in skin fibroblast from aged donors.

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Year:  1989        PMID: 2601414     DOI: 10.1016/0047-6374(89)90011-0

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN: 0047-6374            Impact factor:   5.432


  7 in total

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2.  Adenosine A1 receptors mediate mobilization of calcium in human bronchial smooth muscle cells.

Authors:  Michael F Ethier; J Mark Madison
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4.  Fine-tuning autophagy maximises lifespan and is associated with changes in mitochondrial gene expression in Drosophila.

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5.  Identification of biomarkers of brown adipose tissue aging highlights the role of dysfunctional energy and nucleotide metabolism pathways.

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6.  Iron accumulation with age alters metabolic pattern and circadian clock gene expression through the reduction of AMP-modulated histone methylation.

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Review 7.  Macrophages and the maintenance of homeostasis.

Authors:  David M Mosser; Kajal Hamidzadeh; Ricardo Goncalves
Journal:  Cell Mol Immunol       Date:  2020-09-15       Impact factor: 22.096

  7 in total

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