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Mol Hum Reprod ; 18(8): 391-400, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22362117

RESUMO

Invasion of uterine tissues by extravillous trophoblast cells (EVT) is essential for successful human pregnancy. EVT invasion is tightly regulated by a number of factors, including growth factors and cytokines, but the mechanisms that underlie their regulatory effect remain poorly understood. Interleukin (IL)-6 has been suggested to play a role in controlling EVT invasion. We hypothesized that IL-6 produced by cells in uterine decidua would regulate EVT invasiveness via IL-6Rα and gp130 receptors expressed by trophoblast cells. The effect of IL-6 on EVT signalling and cytokine production was also studied. Supernatants from disaggregated 'total' decidual cells, CD8(+) T cells, CD10(+) decidual stromal cells, CD14 macrophages, CD56(+) uterine natural killer cells, cytotrophoblast and EVT cells contained large quantities of IL-6 protein at both 8-10 and 12-14 weeks gestational age. IL-6Rα and gp130 were immunolocalized to EVT in placental bed biopsies from 8 to 20 weeks gestation and IL-6Rα expression was confirmed by western blotting. IL-6 had no effect on the invasive potential of EVT from chorionic villi or the immortalized EVT cell line HTR-8/SVneo in a Matrigel(®) invasion assay. IL-6 stimulated phosphorylation of several cell signalling proteins in EVT (8-14 weeks' gestation), although significance was lost after correction for multiple comparisons. Incubation with IL-6 decreased secretion of regulated upon activation, normal T-cell expressed and secreted (RANTES) by EVT cells. In conclusion, although IL-6 did not affect trophoblast cell invasion, it stimulated EVT cellular cascades and inhibited secretion of RANTES involved in a number of cellular processes.


Assuntos
Implantação do Embrião/fisiologia , Interleucina-6/metabolismo , Receptores de Interleucina-6/metabolismo , Trofoblastos/fisiologia , Antígeno CD56/biossíntese , Linfócitos T CD8-Positivos/metabolismo , Linhagem Celular , Movimento Celular/fisiologia , Quimiocina CCL5/biossíntese , Quimiocina CCL5/metabolismo , Vilosidades Coriônicas , Receptor gp130 de Citocina/biossíntese , Receptor gp130 de Citocina/metabolismo , Decídua/metabolismo , Feminino , Humanos , Células Matadoras Naturais/metabolismo , Receptores de Lipopolissacarídeos/biossíntese , Macrófagos/metabolismo , Neprilisina/biossíntese , Fosforilação , Gravidez , Primeiro Trimestre da Gravidez , Receptores de Interleucina-6/biossíntese , Transdução de Sinais , Células Estromais/metabolismo , Trofoblastos/citologia , Útero/citologia
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