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Fertil Steril ; 103(5): 1363-9, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25813285

RESUMEN

OBJECTIVE: To study the impact of heparins on chemokines in decidualized human endometrial stromal cells (ESCs) in vitro. DESIGN: In vitro experiment. SETTING: Research laboratory. PATIENT(S): Premenopausal women undergoing hysterectomy for benign reasons. INTERVENTION(S): ESCs were isolated from hysterectomy specimens, decidualized in vitro and incubated with unfractionated heparin and low-molecular-weight heparins (LMWHs) as well as tumor necrosis factor (TNF) α or thrombin with or without heparins. MAIN OUTCOME MEASURE(S): Chemokines CXCL1, CXCL5, CXCL8, CCL2, and CCL5 were measured with the use of ELISA, and CXCL5, CXCL8, CCL2, and CCL5 were detected with the use of real-time reverse-transcription polymerase chain reaction. Cell viability was determined with the use of a fluorometric assay. RESULT(S): TNF-α and thrombin stimulated distinct patterns of chemokines in ESCs. Unfractionated heparin and LMWHs attenuated the TNF-α-mediated induction of CXCL8 and enhanced CXCL5, CCL2, and CCL5. The stimulating effect of thrombin on CXCL8 could be inhibited by heparin, whereas heparin had no impact on thrombin-induced CXCL1 and CCL2. Nuclear factor of transcription κB signaling mediated the effects of TNF-α. The effects of thrombin were mediated via extracellular signal-regulated protein kinases 1/2. CONCLUSION(S): Heparins have modulating effects on TNF-α- and thrombin-induced endometrial chemokines, which might have implications in the regulation of endometrial receptivity and early implantation.


Asunto(s)
Quimiocinas/metabolismo , Endometrio/efectos de los fármacos , Heparina/farmacología , Células del Estroma/efectos de los fármacos , Trombina/farmacología , Factor de Necrosis Tumoral alfa/farmacología , Células Cultivadas , Quimiocinas/genética , Quimiocinas/inmunología , Endometrio/inmunología , Endometrio/metabolismo , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Femenino , Regulación de la Expresión Génica , Heparina de Bajo-Peso-Molecular/farmacología , Humanos , FN-kappa B/metabolismo , ARN Mensajero/metabolismo , Transducción de Señal/efectos de los fármacos , Células del Estroma/inmunología , Células del Estroma/metabolismo
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