Fox A, Lee C S, Brandon M R, Meeusen E N
Centre for Animal Biotechnology, School of Veterinary Science, University of Melbourne, Parkville, Victoria, Australia.
Am J Reprod Immunol. 1998 Oct;40(4):295-302. doi: 10.1111/j.1600-0897.1998.tb00421.x.
Previous studies demonstrate increases in the number and granularity of gamma delta T cells within the sheep uterine interplacentomal epithelium during pregnancy. To further characterize their activation and function, gamma delta T-cell receptor (TCR)+ intraepithelial lymphocytes (IELs) from nonpregnant and pregnant uteri were phenotyped extensively. Cytokine mRNA expression in the epithelium and by gamma delta TCR+ IELs isolated from pregnant uteri was also examined.
Cell suspensions were prepared from the uterine interplacentomal epithelium and from the peripheral blood of nonpregnant and pregnant ewes (120-140 days of gestation). Surface marker expression was determined by two-color flow cytometry and cytokine expression determined by reverse transcriptase--polymerase chain reaction.
Uterine gamma delta TCR+ IELs exhibited increased beta 1-integrin expression but decreased leukocyte function associated antigen (LFA)-1 and major histocompatibility complex class I expression during pregnancy. Major histocompatibility complex class II, CD44, CD2, and LFA-3 expression was unchanged during pregnancy, whereas CD25, VLA-4 and L-selectin were never expressed. The same cytokines were expressed in the pregnant and nonpregnant uterine interplacentomal epithelium with detectable mRNA for interferon (IFN)-gamma, tumor necrosis factor (TNF)-alpha, and interleukin (IL)-1 alpha, but not for IL-2 or IL-4. gamma delta TCR+ and CD8+ IEL purified from pregnant uteri expressed mRNA for IFN-gamma, TNF-alpha, transforming growth factor-beta, and IL-10.
gamma delta TCR+ IELs from pregnant uteri have cytoplasmic granules, and express CD8 and cytokines indicative of cytotoxic potential. Phenotypic changes induced during pregnancy differed from those observed after activation of circulating naive cells and may represent further stimulation of fully differentiated effectors. gamma delta TCR+ IELs are present only in interplacentomal areas of pregnant uteri and may control trophoblast invasion within these areas.
先前的研究表明,在妊娠期间,绵羊子宫胎盘间上皮内γδT细胞的数量和颗粒度会增加。为了进一步表征它们的激活和功能,对来自未怀孕和怀孕子宫的γδT细胞受体(TCR)+上皮内淋巴细胞(IEL)进行了广泛的表型分析。还检测了从怀孕子宫分离的上皮细胞和γδTCR+IEL中的细胞因子mRNA表达。
从未怀孕和怀孕母羊(妊娠120 - 140天)的子宫胎盘间上皮和外周血制备细胞悬液。通过双色流式细胞术测定表面标志物表达,通过逆转录 - 聚合酶链反应测定细胞因子表达。
妊娠期间,子宫γδTCR+IEL表现出β1整合素表达增加,但白细胞功能相关抗原(LFA)-1和主要组织相容性复合体I类表达降低。主要组织相容性复合体II类、CD44、CD2和LFA-3表达在妊娠期间未发生变化,而CD25、VLA-4和L-选择素从未表达。在怀孕和未怀孕的子宫胎盘间上皮中表达相同的细胞因子,可检测到干扰素(IFN)-γ、肿瘤坏死因子(TNF)-α和白细胞介素(IL)-1α的mRNA,但未检测到IL-2或IL-4的mRNA。从怀孕子宫中纯化的γδTCR+和CD8+IEL表达IFN-γ、TNF-α、转化生长因子-β和IL-10的mRNA。
来自怀孕子宫的γδTCR+IEL具有细胞质颗粒,并表达CD8和具有细胞毒性潜力的细胞因子。妊娠期间诱导的表型变化与循环幼稚细胞激活后观察到的变化不同,可能代表对完全分化效应细胞的进一步刺激。γδTCR+IEL仅存在于怀孕子宫的胎盘间区域,可能控制这些区域内的滋养层侵入。