Publicación: ELEVATED PRO-ANGIOGENIC PHENOTYPE IN FETO-PLACENTAL TISSUE FROM GESTATIONAL DIABETES MELLITUS
dc.creator | JESENIA MARIANELA ACURIO JÁCOME | |
dc.creator | KURT ERWIN HERLITZ FLORES | |
dc.creator | CARLOS ALONSO ESCUDERO OROZCO | |
dc.date | 2015 | |
dc.date.accessioned | 2025-01-10T14:38:00Z | |
dc.date.available | 2025-01-10T14:38:00Z | |
dc.date.issued | 2015 | |
dc.description.abstract | OBJECTIVE: WE AIMED TO INVESTIGATE WHETHER FETO-PLACENTAL TISSUE FROM GESTATIONAL DIABETES MELLITUS (GDM) EXHIBITS AN ELEVATED PRO-ANGIOGENIC PHENOTYPE COMPARED TO NORMAL PREGNANCY. METHODS: WE OBTAINED PLACENTAL SAMPLES FROM NORMAL PREGNANT WOMEN (N=12) AND GDM PATIENTS (N=14), WHICH WERE HOMOGENIZED TO OBTAIN MRNA AND PROTEIN EXTRACTIONS. SEMI-QUANTITATIVE PCR WAS PERFORMED TO ESTIMATE MRNA LEVELS OF VEGF, VEGFR TYPE 1 (VEGFR1) AND VEGFR2. ALSO, PROTEIN CONCENTRATIONS OF CD31, CD34, KI67, VEGF, VEGFR1, VEGFR2 AND Y951-PHOSPHORYLATED VEGFR2 WERE ESTIMATED BY WESTERN BLOT. Y1175 PHOSPHORYLATED VEGFR2 WAS MEASURED BY ELISA. ALSO HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS (HUVEC) WERE ISOLATED FROM NORMAL (N=10) AND GDM (N=10) WOMAN. CELL PROLIFERATION WAS ANALYZED BY COLORIMETRIC MTS-ASSAY (PROMEGA, USA), WHEREAS MIGRATION WAS ANALYZED BY CELL-SCRATCH ASSAY AFTER 24 HOURS OF CELL INCUBATION WITHOUT ANY TREATMENT. | |
dc.format | application/pdf | |
dc.identifier.doi | 10.1016/j.placenta.2015.01.436 | |
dc.identifier.issn | 1532-3102 | |
dc.identifier.issn | 0143-4004 | |
dc.identifier.uri | https://repositorio.ubiobio.cl/handle/123456789/8282 | |
dc.language | spa | |
dc.publisher | PLACENTA | |
dc.relation.uri | 10.1016/j.placenta.2015.01.436 | |
dc.rights | PUBLICADA | |
dc.title | ELEVATED PRO-ANGIOGENIC PHENOTYPE IN FETO-PLACENTAL TISSUE FROM GESTATIONAL DIABETES MELLITUS | |
dc.type | ARTÍCULO | |
dspace.entity.type | Publication | |
ubb.Estado | PUBLICADA | |
ubb.Otra Reparticion | DEPARTAMENTO DE CIENCIAS BASICAS | |
ubb.Otra Reparticion | DEPARTAMENTO DE CIENCIAS BASICAS | |
ubb.Sede | CHILLÁN | |
ubb.Sede | CHILLÁN |