dc.creator | Pagano, Eleonora Samanta | |
dc.creator | Coso, Omar Adrian | |
dc.creator | Calvo, Juan Carlos | |
dc.date.accessioned | 2017-10-02T15:49:41Z | |
dc.date.accessioned | 2018-11-06T11:21:26Z | |
dc.date.available | 2017-10-02T15:49:41Z | |
dc.date.available | 2018-11-06T11:21:26Z | |
dc.date.created | 2017-10-02T15:49:41Z | |
dc.date.issued | 2008-05 | |
dc.identifier | Pagano, Eleonora Samanta; Coso, Omar Adrian; Calvo, Juan Carlos; Down-modulation of erbB2 activity is necessary but not enough in the differentiation of 3T3-L1 preadipocytes; Wiley; Journal of Cellular Biochemistry; 104; 1; 5-2008; 274-285 | |
dc.identifier | 0730-2312 | |
dc.identifier | http://hdl.handle.net/11336/25565 | |
dc.identifier | 1097-4644 | |
dc.identifier | CONICET Digital | |
dc.identifier | CONICET | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1849280 | |
dc.description.abstract | The high incidence of obesity-related pathologies, led to the study of the mechanisms involved in preadipose cell proliferation and differentiation. Here, we demonstrate that modulation of erbB2, plays a fundamental role during proliferation and adipogenic induction of preadipocytes. Using 3T3-L1 cells as model, we demonstrate that EGF (10 nM, 5 min) in addition to stimulate receptor tyrosine phosphorylation of both erbB2 and EGFR, is able to induce the heterodimer erbB2-EGFR. We treated proliferating 3T3-L1 cells with two inhibitors, AG 825 (IC(50) 0.35 microM, 54 times more selective for erbB2 than for EGFR, IC(50) 19 microM), and AG 879 (IC(50) of 1 microM for erbB2 versus 500 microM for EGFR). We found that both inhibited the proliferation on a dose-dependent basis, reaching a 30% maximal inhibition at 100 microM (P < 0.001) for AG825, and a 20% maximal inhibition at 10 microM (P < 0.001) for AG 879. These results involve erbB2 in 3T3-L1 proliferation. When studying the differentiation process, we found that the action of MIX-Dexa immediately activates MEK, JNK and p38 kinases. We observed that PD98059 and SP600125 (MEK-ERK and JNK inhibitors, respectively) added 1 h prior to the MIX-Dexa induction produced a decrease in erbB2 expression after 6 h, which is even greater than the one produced by the inducers, MIX-Dexa. This work supports erbB2 as a key factor in 3T3-L1 adipogenesis, acting mostly and not only during the proliferative phase but also during the differentiation through modulation of both its expression and activity. | |
dc.language | eng | |
dc.publisher | Wiley | |
dc.relation | info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcb.21621/abstract | |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/jcb.21621 | |
dc.relation | info:eu-repo/semantics/altIdentifier/url/17990290 | |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | erB2 | |
dc.subject | EGFR/erB1 | |
dc.subject | THYRPHOSTIN | |
dc.subject | ADYPOCYTES | |
dc.subject | GENE EXPRESSION REGULATION | |
dc.subject | CELL DIFFERENTIATION | |
dc.title | Down-modulation of erbB2 activity is necessary but not enough in the differentiation of 3T3-L1 preadipocytes | |
dc.type | Artículos de revistas | |
dc.type | Artículos de revistas | |
dc.type | Artículos de revistas | |