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Lipid peroxidation-derived 4-hydroxynonenal-modified proteins accumulate in human facial skin fibroblasts during ageing in vitro (CROSBI ID 199279)

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Jørgensen, Peter ; Milković, Lidija ; Žarković, Neven ; Waeg, Georg ; Rattan, Suresh, I.S. Lipid peroxidation-derived 4-hydroxynonenal-modified proteins accumulate in human facial skin fibroblasts during ageing in vitro // Biogerontology (Dordrecht), 15 (2014), 1; 105-110. doi: 10.1007/s10522-013-9482-z

Podaci o odgovornosti

Jørgensen, Peter ; Milković, Lidija ; Žarković, Neven ; Waeg, Georg ; Rattan, Suresh, I.S.

engleski

Lipid peroxidation-derived 4-hydroxynonenal-modified proteins accumulate in human facial skin fibroblasts during ageing in vitro

The reactive aldehyde, 4-hydroxynonenal (HNE), is recognized as a product of lipid peroxidation, which binds to macromolecules, in particular proteins. HNE-modified proteins (HNE-MP) have been shown to accumulate during ageing, generally by using polyclonal antibodies, which increase the possibility of detecting false positives. Therefore, we have used a genuine monoclonal antibody specific for HNE-His adducts of proteins/peptides, which were revealed by immunoblotting method for whole-cell HNE-MP measurements in serially passaged human facial skin fibroblasts undergoing ageing in vitro. There was a significant increase in the levels of HNE-MP in serially passaged cells approaching a near senescent state at high passage level (P-61), as compared with low passage level (P-11) young and middle-aged (P-27) cells. However, if the cells were analyzed soon after re-initiation from the frozen samples with little further passaging, the amount of HNE-MP was low even in relatively high passage level (P-37) cells, which is an indication of selective elimination of cells with high molecular damage during the process of thawing and re-initiation in culture. This pilot study on normal human facial skin fibroblasts shows that HNE-MP detection by monoclonal antibody-based dot blot method can be used as a marker for age-related accumulation of lipid peroxidative molecular damage, and could be useful for testing and monitoring the effects of potential skin care products on ageing parameters.

ageing ; intervention ; senescence ; lipid peroxidation ; molecular damage

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Podaci o izdanju

15 (1)

2014.

105-110

objavljeno

1389-5729

1573-6768

10.1007/s10522-013-9482-z

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Kemija

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