Dudley D J, Edwin S S, Mitchell M D
Department of Obstetrics and Gynecology, University of Utah School of Medicine, Salt Lake City 84132, USA.
J Soc Gynecol Investig. 1996 Jan-Feb;3(1):12-6. doi: 10.1016/1071-5576(95)00042-9.
To determine if the inflammatory cytokine macrophage inflammatory protein-1 alpha (MLP-1 alpha) stimulates the production of prostaglandin E2 (PGE2) and interleukin-6 (IL-6) by human gestational tissues.
Human decidual cells, chorion cells, and amnion cells were isolated from term placentas of women with normal pregnancies, and primary cultures of each cell line were established. In various concentrations, MIP-1 alpha was then applied to each cell culture for 16 hours at 37C, and culture supernatants were assayed for PGE2 and IL-6.
After incubation with MIP-1 alpha, decidual cells produced increased amounts of both IL-6 (P < .05) but not PGE2. When subjected to similar conditions, chorion cells produced increased amounts of both IL-6 and PGE2 (P < .05). Conversely, amnion cells produced increased amounts of only PGE2 in response to increasing concentrations of MIP-1 alpha (P < .05).
Maternal and fetal gestational tissues differentially respond to MIP-1 alpha with regard to PGE2 and IL-6 production; MIP-1 alpha may play a role in both the initiation and propagation of the inflammatory response associated with intrauterine infection.
确定炎性细胞因子巨噬细胞炎性蛋白 -1α(MIP -1α)是否刺激人妊娠组织产生前列腺素E2(PGE2)和白细胞介素 -6(IL -6)。
从正常妊娠妇女足月胎盘中分离出人蜕膜细胞、绒毛膜细胞和羊膜细胞,并建立每种细胞系的原代培养。然后将不同浓度的MIP -1α在37℃下应用于每种细胞培养16小时,并检测培养上清液中的PGE2和IL -6。
用MIP -1α孵育后,蜕膜细胞产生的IL -6量增加(P <.05),但PGE2未增加。在类似条件下,绒毛膜细胞产生的IL -6和PGE2量均增加(P <.05)。相反,随着MIP -1α浓度增加,羊膜细胞仅产生增加量的PGE2(P <.05)。
母体和胎儿妊娠组织在PGE2和IL -6产生方面对MIP -1α有不同反应;MIP -1α可能在与宫内感染相关的炎症反应的起始和传播中起作用。