Can oxygen tension contribute to an abnormal placental cytokine milieu?
Can oxygen tension contribute to an abnormal placental cytokine milieu?
复制标题
氧张力会导致胎盘细胞因子环境异常吗?
DOI:
10.1111/j.1600-0897.2011.00998.x
复制
发表时间:
2011
期刊:
影响因子:
--
通讯作者:
Hanna,Nazeeh
中科院分区:
文献类型:
--
作者:
Peltier,MorganR;Gurzenda,EllenM;Murthy,Amitasrigowri;Chawala,Kiranpreet;Lerner,Veronica;Kharode,Ishita;Arita,Yuko;Rhodes,Adam;Maari,Nisreen;Moawad,Andrew;Hanna,Nazeeh
CitationPeltier MR, Gurzenda EM, Murthy A, Chawala K, Lerner V, Kharode I, Arita Y, Rhodes A, Maari N, Moawad A, Hanna N. Can oxygen tension contribute to an abnormal placental cytokine milieu? Am J Reprod Immunol 2011; 66: 279–285ObjectiveThe aim of this study was to determine whether culturing human placental explants under different oxygen tensions will alter expression of pro‐ and anti‐inflammatory mediators.MethodsPlacental explant cultures from second‐trimester, elective, terminations‐of‐pregnancy were incubated under 21, 5, or 1% O2concentrations for 24 hr in the presence or absence of IL‐10. Cytokine concentrations in the conditioned medium were quantified by immunoassay.ResultsCulture of placental explants under 21, 5, or 1% O2concentrations produced hyperoxic (143 ± 1.6 mmHg), normoxic (37 ± 1.6 mmHg), and hypoxic (18.2 ± 1.6 mmHg) pO2levels for the maternal–fetal interface in the medium. Oxygen tension had profound effects on basal placental cytokine levels as well as on IL‐10‐stimulated cytokine production. IL‐1β and TNF‐α, but not IFN‐γ production, was reduced by 21% O2. Moreover, 21% O2levels increased the anti‐inflammatory cytokines IL‐10 and IL‐13 while 1% O2tended to decrease the production of these cytokines.ConclusionsFive percent‐ O2incubation more accurately representsin vivopO2conditions at the maternal–fetal interface. Routine culture of placental explants in room air produces a superphysiologic oxygen tension that tended to increase the production of anti‐inflammatory and decrease the production of pro‐inflammatory cytokines. In addition, low pO2may reduce responsiveness of the placenta to the anti‐inflammatory actions of IL‐10.