Zaga-Clavellina Veronica, Parra-Covarrubias Adalberto, Ramirez-Peredo Jorge, Vega-Sanchez Rodrigo, Vadillo-Ortega Felipe
Department of Cell Biology, Instituto Nacional de Perinatología Isidro Espinosa de los Reyes, Mexico City, Mexico.
Department of Endocrinology, Instituto Nacional de Perinatología Isidro Espinosa de los Reyes, Mexico City, Mexico.
Am J Obstet Gynecol. 2014 Jul;211(1):48.e1-6. doi: 10.1016/j.ajog.2014.01.039. Epub 2014 Feb 1.
To test the effect of prolactin (PRL) on expression of proinflammatory cytokines and matrix metallopeptidase 9 (MMP-9) in vitro.
Tissue explants were incubated from 4 to 48 hours alone or in the presence of 500 ng/mL PRL, and mRNA expression in tissues and secretion of interleukin (IL)-1β, tumor necrosis factor alpha (TNF-α), MMP-2, and MMP-9 was quantified.
Fetal membranes secreted IL-1β, TNF-α, and MMP-9 in culture with consistent low concentration during the first 24 hours and then increased progressively. The presence of PRL during explant incubation significantly decreased the patterns of IL-1β, TNF-α and MMP-9 secretion along culture (P < .001). MMP-2 secretion was unaffected by PRL. The relative basal expression of IL-1β mRNA (1.2 ± 0.87) was reduced by 80% in the presence of PRL after 32 hours of incubation of the membranes (P = .001). The expression of the TNF-α mRNA was not modified by the presence of PRL (0.06 ± 0.01) compared with the basal expression levels (0.05 ± 0.01). MMP-9 mRNA basal expression (0.018 ± 0.008) was significantly reduced (P = .001) in the presence of PRL after 32 hours (0.002 ± 0.0005).
PRL may be a potential candidate as a key signal controlling the expression of signals related to the proinflammatory reaction associated with human labor.
在体外检测催乳素(PRL)对促炎细胞因子和基质金属蛋白酶9(MMP-9)表达的影响。
将组织外植体单独培养4至48小时,或在500 ng/mL PRL存在的情况下培养,对组织中的mRNA表达以及白细胞介素(IL)-1β、肿瘤坏死因子α(TNF-α)、MMP-2和MMP-9的分泌进行定量分析。
胎膜在培养过程中分泌IL-1β、TNF-α和MMP-9,最初24小时浓度持续较低,随后逐渐升高。外植体培养期间PRL的存在显著降低了培养过程中IL-1β、TNF-α和MMP-9的分泌模式(P <.001)。MMP-2的分泌不受PRL影响。胎膜培养32小时后,在PRL存在的情况下,IL-1β mRNA的相对基础表达(1.2±0.87)降低了80%(P =.001)。与基础表达水平(0.05±0.01)相比,PRL的存在未改变TNF-α mRNA的表达(0.06±0.01)。32小时后,在PRL存在的情况下,MMP-9 mRNA基础表达(0.018±0.008)显著降低(P =.001)(0.002±0.0005)。
PRL可能是控制与人类分娩相关的促炎反应相关信号表达的关键信号的潜在候选者。