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Preferential reduction of the alpha-2-6-sialylation from cell surface N-glycans of human diploid fibroblastic cells by in vitro aging. | LitMetric

AI Article Synopsis

  • The TIG-3 human diploid fibroblastic cell line is used to study aging and has a limited lifespan of about 80 population doublings (PDL).
  • Research shows that younger cells (PDL 23) grow faster and reach higher densities compared to older cells (PDL 77), which shows decreased negative surface charge.
  • Analysis indicated a significant reduction in alpha-2,6-sialylation of N-glycans in aged cells, linked to decreased expression of the gene ST6Gal I, responsible for adding sialic acid to these molecules.

Article Abstract

Human diploid fibroblastic cell line, TIG-3, has a finite life span of about 80 population doubling levels (PDL), and is used for in vitro aging studies. Young cells (PDL 23) grew to higher cell densities at a higher growth rate than aged cells (PDL 77). When the electrophoretic mobility of cells was determined, the negative surface charge of the aged cells decreased significantly when compared to that of young cells. Lectin blot analysis of membrane glycoproteins showed that the alpha-2-6-sialylation but not the alpha-2-3-sialylation of N-glycans decreases markedly in the aged cells when compared to the young cells. In support of this observation, the cDNA microarray assay and reverse transcription-polymerase chain reaction (RT-PCR) analysis showed that the gene expression of the alpha-2,6-sialyltransferase I (ST6Gal I), which transfers sialic acid to galactose residues of N-glycans, decreases in the aged cells. These results indicate that the concordant decrease of the alpha-2,6-sialylation of N-glycans with the ST6Gal I gene expression is induced in TIG-3 cells by in vitro aging.

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Source
http://dx.doi.org/10.1007/s10719-006-7152-yDOI Listing

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