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Title:Hypoxia influences the cellular cross-talk of human dermal fibroblasts. A proteomic approach.
Authors:ID Federica, Boraldi, University of Modena and Reggio Emilia (Author)
ID Giulia, Annovi, University of Modena and Reggio Emilia (Author)
ID Fabio, Carraro, University of Siena (Author)
ID Antonella, Naldini, University of Siena (Author)
ID Roberta, Tiozzo, University of Modena and Reggio Emilia (Author)
ID Pascal, Sommer, Université Lyon I (Author)
ID Daniela, Quaglino, University of Modena and Reggio Emilia (Author), et al.
Files: This document has no files that are freely available to the public. This document may have a physical copy in the library of the organization, check the status via COBISS. Link is opened in a new window
Language:English
Work type:Not categorized
Typology:1.01 - Original Scientific Article
Organization:UNG - University of Nova Gorica
Abstract:The ability of cells to respond to changes in oxygen availability is critical for many physiological and pathological processes (i.e. development, aging, wound healing, hypertension, cancer). Changes in the protein profile of normal human dermal fibroblasts were investigated in vitro after 96 h in 5% CO2 and 21% O2 (pO2=140 mm Hg) or 2% O2 (pO2=14 mm Hg), these parameters representing a mild chronic hypoxic exposure which fibroblasts may undergo in vivo. The proliferation rate and the protein content were not significantly modified by hypoxia, whereas proteome analysis demonstrated changes in the expression of 56 proteins. Protein identification was performed by mass spectrometry. Data demonstrate that human fibroblasts respond to mild hypoxia increasing the expression of hypoxia inducible factor (HIF1a) and of the 150-kDa oxygen-regulated protein. Other differentially expressed proteins appeared to be related to stress response, transcriptional control, metabolism, cytoskeleton, matrix remodelling and angiogenesis. Furthermore, some of them, like galectin 1, 40S ribosomal protein SA, N-myc-downstream regulated gene-1 protein, that have been described in the literature as possible cancer markers, significantly changed their expression also in normal hypoxic fibroblasts. Interestingly, a bovine fetuin was also identified that appeared significantly less internalised by hypoxic fibroblasts. In conclusion, results indicate that human dermal fibroblasts respond to an in vitro mild chronic hypoxic exposure by modifying a number of multifunctional proteins. Furthermore, data highlight the importance of stromal cells in modulating the intercellular cross-talk occurring in physiological and in pathologic conditions.
Keywords:Human fibroblast, Primary cell culture, Hypoxia, Connective tissue, Proteome, 2D gel electrophoresis, Mass-spectrometry
Year of publishing:2007
Number of pages:1402-1413
Numbering:1774
PID:20.500.12556/RUNG-4662-9db8e07b-5b5c-b597-fdde-e297308468a4 New window
COBISS.SI-ID:5425147 New window
NUK URN:URN:SI:UNG:REP:YJMYQ6CC
Publication date in RUNG:22.07.2019
Views:3464
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Record is a part of a journal

Title:Biochimica et Biophysica Acta
Shortened title:BBA
Year of publishing:2007

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License:CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.
Licensing start date:19.07.2019

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