Madhukaran Shanmuga Priyaa, Koippallil Gopalakrishnan Aghila Rani, Pandit Hrishikesh, Marri Eswari Dodagatta-, Kouser Lubna, Jamil Kaiser, Alhamlan Fatimah S, Kishore Uday, Madan Taruna
Department of Innate Immunity, National Institute for Research in Reproductive Health, Mumbai 400 012, India; Centre for Biotechnology and Bioinformatics, School of Life Sciences, Jawaharlal Nehru Institute for Advanced Studies, Secunderabad, Telangana, India; Centre for Infection, Immunity and Disease Mechanisms, College of Health and Life Science, Brunel University London, Uxbridge, UB8 3PH, United Kingdom.
Department of Innate Immunity, National Institute for Research in Reproductive Health, Mumbai 400 012, India.
Immunobiology. 2016 Feb;221(2):377-86. doi: 10.1016/j.imbio.2015.09.019. Epub 2015 Sep 16.
Surfactant proteins SP-A and SP-D are pattern recognition innate immune molecules that belong to the C-type lectin family. In lungs, they play an important role in the clearance of pathogens and control of inflammation. SP-A and SP-D are also expressed in the female reproductive tract where they play an important role in pregnancy and parturition. However, the role of SP-A and SP-D expressed at the feto-maternal interface (decidua) remains unclear. Here, we have examined the expression of SP-A and SP-D in the murine decidua at 17.5 (pre-parturition) and 19.5dpc (near parturition) and their effect on lipopolysaccharide (LPS)-treated decidual macrophages. SP-A and SP-D were localized to stromal cells in the murine decidua at 17.5 and 19.5dpc in addition to cells lining the maternal spiral artery. Purified pre-parturition decidual cells were challenged with LPS with and without SP-A or SP-D, and expression of F4/80 and TNF-α were measured by flow cytometry. On their own, SP-A or SP-D did not affect the percentage of F4/80 positive cells while they suppressed the percentage of TNF-α positive cells. However, simultaneous addition of SP-A or SP-D, together with LPS, reduced TNF-α secreting F4/80 positive cells. It is likely that exogenous administration of SP-A and SP-D in decidua can potentially control infection and inflammation mediators during spontaneous term labor and infection-induced preterm labor. Thus, the presence of SP-A and SP-D in the murine decidua is likely to play a protective role against intrauterine infection during pregnancy.
表面活性蛋白SP-A和SP-D是属于C型凝集素家族的模式识别天然免疫分子。在肺部,它们在病原体清除和炎症控制中发挥重要作用。SP-A和SP-D也在女性生殖道中表达,在妊娠和分娩过程中发挥重要作用。然而,在母胎界面(蜕膜)表达的SP-A和SP-D的作用仍不清楚。在此,我们检测了17.5天(临产前)和19.5天妊娠日(临近分娩)时小鼠蜕膜中SP-A和SP-D的表达及其对脂多糖(LPS)处理的蜕膜巨噬细胞的影响。除了母螺旋动脉内衬的细胞外,在17.5天和19.5天妊娠日时,SP-A和SP-D定位于小鼠蜕膜的基质细胞。用LPS处理纯化的临产前蜕膜细胞,同时添加或不添加SP-A或SP-D,通过流式细胞术检测F4/80和TNF-α的表达。单独的SP-A或SP-D不影响F4/80阳性细胞的百分比,但它们抑制了TNF-α阳性细胞的百分比。然而,同时添加SP-A或SP-D与LPS一起,可减少分泌TNF-α的F4/80阳性细胞。在足月自然分娩和感染诱导的早产期间,向蜕膜中外源性施用SP-A和SP-D可能潜在地控制感染和炎症介质。因此,小鼠蜕膜中SP-A和SP-D的存在可能在孕期对子宫内感染起到保护作用。