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Selective increase of α2-integrin sub-unit expression on human carcinoma cells upon EGF-receptor activation

✍ Scribed by Kirstin Krensel; Rosemarie B. Lichtner


Book ID
101233980
Publisher
John Wiley and Sons
Year
1999
Tongue
French
Weight
277 KB
Volume
80
Category
Article
ISSN
0020-7136

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✦ Synopsis


The effects of chronic EGF exposure on expression of the ␣ 2 ␤ 1 collagen and ␣ 5 ␤ 1 fibronectin receptor in a pair of human carcinoma cell lines (A431 and A549) with differential responses to EGF in a short-term ECM-cell adhesion assay were investigated. Treatment with EGF at 10 ng/ml for 24 hr increased on both cell lines the expression of the ␣ 2 -but not the ␤ 1 -or ␣ 5 -integrin sub-units, and concomitantly cellular adhesion was increased on collagen IV but not on fibronectin.

Increased collagen adhesion of A549 cells could be blocked by

␣ 2 -and ␤ 1 -integrin-sub-unit antibodies down to control levels, while it was blocked by ␣ 2 -integrin-sub-unit antibody only by 60% and completely by the ␤ 1 -integrin-sub-unit antibody on A431 cells. EGF induced disparate shifts in cell morphologies (dome-like structures, A431, vs. spindle-like fibroblastoid, A549) with concomitant opposite changes in the expression/ localization of E-cadherin in cell-cell contacts. This could be taken as an indication for cell-type-specific differential changes in the ratio of cell-ECM vs. cell-cell contacts. The EGFinduced up-regulation of the ␣ 2 ␤ 1 integrin was instrumental in increasing collagen adhesion of A549 but only partly in the case of A431 cells, in which cells the ␣ 2 ␤ 1 integrin may have additional functions besides serving as cell-ECM receptor. Int.


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