D-Glucose stimulation of L-arginine transport and nitric oxicle synthesis results from activation of mitogen-activated protein kinases p42/44 and smad2 requiring functional type II TGF-beta receptors in human umbilical vein endothelium
dc.contributor.author | Vasquez, Rodrigo | |
dc.contributor.author | Farias, Marcelo | |
dc.contributor.author | Vega, Jost Luis | |
dc.contributor.author | Martin, Rody San | |
dc.contributor.author | Vecchiola, Andrea | |
dc.contributor.author | Casanello, Paola | |
dc.contributor.author | Sobrevia, Luis | |
dc.date.accessioned | 2024-01-10T13:12:18Z | |
dc.date.available | 2024-01-10T13:12:18Z | |
dc.date.issued | 2007 | |
dc.description.abstract | Elevated extracellular D-glucose increases transforming growth factor P I (TGF-P 1) release from human umbilical vein endothelium (HUVEC). TGF-P 1, via TGF-P receptors I (T beta RI) and T beta RII, activates Smad2 and mitogen -activated protein kinases p44 and p42 (p42/44 (mapk)). We studied whether D-glucose-stimulation Of L-arginine transport and nitric oxide synthesis involves TGF-beta 1 in primary cultures of HUVEC. TGF-P I release was higher (similar to 1.6-fold) in 25 mM (high) compared with 5 mM (normal) D-glucose. TGF-P I increases L-arginine transport (half maximal effect similar to 1.6 ng/ml) in normal D-glucose, but did not alter high D-glucose-increased L-arginine transport. TGF-P I and high D-glucose increased hCAT- I mRNA expression (similar to 8-fold) and maximal transport velocity (V-max), L- [(3) H]citrulline formation from L- [3 H]arginine (index of NO synthesis) and endothelial NO synthase (eNOS) protein abundance, but did not alter eNOS phosphorylation. TGF-beta 1 I and high D-gludose increased p42/44 mapk and Smad2 phosphorylation, an effect blocked by PD-98059 (MEK 1 /2 inhibitor). However, TGF-P I and high D-glucose were ineffective in cells expressing a truncated, negative dominant T beta RII High D-glucose increases L-arginine transport and eNOS expression following T beta RII activation by TGF-P I involving p42/44 (mapk) and Smad2 in HUVEC. Thus, TGF-P I could play a crucial role under conditions of hyperglycemia, such as gestational diabetes mellitus, which is | |
dc.format.extent | 7 páginas | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1002/jcp.21057 | |
dc.identifier.eissn | 1097-4652 | |
dc.identifier.issn | 0021-9541 | |
dc.identifier.pubmedid | MEDLINE:17427197 | |
dc.identifier.uri | https://doi.org/10.1002/jcp.21057 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/78167 | |
dc.identifier.wosid | WOS:000248770500009 | |
dc.information.autoruc | Medicina;Casanello P;S/I;146772 | |
dc.information.autoruc | Medicina;Farías M;S/I;12286 | |
dc.information.autoruc | Medicina;San Martin R;S/I;1003218 | |
dc.information.autoruc | Medicina;Sobrevia L;S/I;1002656 | |
dc.information.autoruc | Ciencias Biológicas;Vecchiola A;S/I;123319 | |
dc.information.autoruc | Ciencias Biológicas;Vega J;S/I;165832 | |
dc.information.autoruc | Ciencias Biológicas;Vásquez R;S/I;6 | |
dc.issue.numero | 3 | |
dc.language.iso | en | |
dc.nota.acceso | Sin adjunto | |
dc.pagina.final | 632 | |
dc.pagina.inicio | 626 | |
dc.publisher | WILEY | |
dc.revista | JOURNAL OF CELLULAR PHYSIOLOGY | |
dc.rights | registro bibliográfico | |
dc.subject | GROWTH-FACTOR-BETA | |
dc.subject | SMOOTH-MUSCLE-CELLS | |
dc.subject | OXIDE SYNTHASE EXPRESSION | |
dc.subject | SIGNAL-REGULATED KINASE | |
dc.subject | HUMAN MESANGIAL CELLS | |
dc.subject | AMINO-ACID | |
dc.subject | ACUTE HYPERGLYCEMIA | |
dc.subject | VASODILATION | |
dc.subject | DYSFUNCTION | |
dc.subject | TGF-BETA-1 | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | D-Glucose stimulation of L-arginine transport and nitric oxicle synthesis results from activation of mitogen-activated protein kinases p42/44 and smad2 requiring functional type II TGF-beta receptors in human umbilical vein endothelium | |
dc.type | artículo | |
dc.volumen | 212 | |
sipa.codpersvinculados | 146772 | |
sipa.codpersvinculados | 12286 | |
sipa.codpersvinculados | 1003218 | |
sipa.codpersvinculados | 1002656 | |
sipa.codpersvinculados | 123319 | |
sipa.codpersvinculados | 165832 | |
sipa.codpersvinculados | 6 | |
sipa.index | WOS | |
sipa.index | Scopus | |
sipa.trazabilidad | Carga SIPA;09-01-2024 |
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