Microarray-based identification of age-dependent differences in gene expression of human dermal fibroblasts.

Abstract:

:Senescence is thought to play an important role in the progressive age-related decline in tissue integrity and concomitant diseases, but not much is known about the complex interplay between upstream regulators and downstream effectors. We profiled whole genome gene expression of non-stressed and rotenone-stressed human fibroblast strains from young and oldest old subjects, and measured senescence associated β-gal activity. Microarray results identified gene sets involved in carbohydrate metabolism, Wnt/β-catenin signaling, the cell cycle, glutamate signaling, RNA-processing and mitochondrial function as being differentially regulated with chronological age. The most significantly differentially regulated mRNA corresponded to the p16 gene. p16 was then investigated using qPCR, Western blotting and immunocytochemistry. In conclusion, we have identified cellular pathways that are differentially expressed between fibroblast strains from young and old subjects.

journal_name

Mech Ageing Dev

authors

Dekker P,Gunn D,McBryan T,Dirks RW,van Heemst D,Lim FL,Jochemsen AG,Verlaan-de Vries M,Nagel J,Adams PD,Tanke HJ,Westendorp RG,Maier AB

doi

10.1016/j.mad.2012.06.002

subject

Has Abstract

pub_date

2012-07-01 00:00:00

pages

498-507

issue

7

eissn

0047-6374

issn

1872-6216

pii

S0047-6374(12)00103-0

journal_volume

133

pub_type

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