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- Audouin, L., et al.
(författare)
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Quantifying differences between computational results and measurements in the case of a large-scale well-confined fire scenario
- 2011
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Ingår i: Nuclear Engineering and Design. - : Elsevier BV. - 1872-759X .- 0029-5493. ; 241:1, s. 18-31
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Tidskriftsartikel (refereegranskat)abstract
- The objective of this work was to quantify comparisons between several computational results and measurements performed during a pool fire scenario in a well-confined compartment. This collaborative work was initiated under the framework of the OECD fire research program and involves the most frequently used fire models in the fire community, including field and zone models. The experimental scenario was conducted at the French Institut de Radioprotection et de Surete Nucleaire (IRSN) and deals with a full-scale liquid pool fire in a confined and mechanically ventilated compartment representative for nuclear plants. The practical use of different metric operators and their ability to report the capabilities of fire models are presented. The quantitative comparisons between measurements and numerical results obtained from "open" calculations concern six important quantities from a safety viewpoint: gas temperature, oxygen concentration, wall temperature, total heat flux, compartment pressure and ventilation flow rate during the whole fire duration. The results indicate that it is important to use more than one metric for the validation process in order to get information on the uncertainties associated with different aspects of fire safety. (C) 2010 Elsevier B.V. All rights reserved.
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- Lallemand, D., et al.
(författare)
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Variations in Jun and Fos protein expression and AP-1 activity in cycling, resting and stimulated fibroblasts
- 1997
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Ingår i: Oncogene. - : Nature Publishing Group. - 0950-9232 .- 1476-5594. ; 14:7, s. 819-830
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Tidskriftsartikel (refereegranskat)abstract
- We have analysed the different Jun and Fos proteins as NIH3T3 fibroblasts pass from exponential growth to quiescence and during the first 24 h after their re-entry into the cell cycle following serum stimulation. We show that these proteins can be divided into 3 subgroups based on their pattern of expression. The first contains c-Jun, Jun-D and Fra-2 which are expressed at high level in cycling cells and are only mildly induced by serum. The second contains Jun-B, c-Fos, Fos-B and deltaFos-B whose levels are low in cycling cells but increase strongly and rapidly after stimulation by serum. The third group contains only Fra-1, which is absent from cycling cells and behaves as a delayed early response protein after serum stimulation. AP-1 binding activity is low both in cycling and quiescent fibroblasts but increases after stimulation by serum with kinetics matching the induction of the various Jun and Fos proteins. Antibody supershift analyses demonstrate that the composition of AP-1 binding activity reflects the relative abundance of each Jun and Fos protein. Furthermore, the state of post-translational modification varies continuously for all of the AP-1 proteins as growth conditions change. These data indicate that AP-1 activity during the G0-G1 transition is finely regulated and complex, involving changes both in protein expression and in posttranslational modification.
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- Pfarr, C. M., et al.
(författare)
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Mouse JunD negatively regulates fibroblast growth and antagonizes transformation by ras
- 1994
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Ingår i: Cell. - : Cell Press. - 0092-8674 .- 1097-4172. ; 76:4, s. 747-760
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Tidskriftsartikel (refereegranskat)abstract
- As NIH 3T3 fibroblasts become quiescent, the level of c-Jun protein decreases while JunD accumulates. When resting cells are stimulated with fresh serum, nuclear-localized JunD is rapidly degraded, followed by resynthesis of both c-Jun and JunD later in G1. Overexpression of JunD results in slower growth and an increase in the percentage of cells in G0/G1 while c-Jun overexpression produces larger S/G2 and M phase populations. In addition, JunD partially suppresses transformation by an activated ras gene whereas c-Jun cooperates with ras to transform cells. These data indicate that two closely related transcription factors can function in an opposing manner.
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