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小鼠子宫中细胞因子基因的差异表达与调控

Differential expression and regulation of cytokine genes in the mouse uterus.

作者信息

Kover K, Liang L, Andrews G K, Dey S K

机构信息

Department of Physiology, Ralph L. Smith Research Center, University of Kansas Medical Center, Kansas City 66160-7338.

出版信息

Endocrinology. 1995 Apr;136(4):1666-73. doi: 10.1210/endo.136.4.7895677.

Abstract

The present investigation examined the differential expression of cytokine genes in vivo and in vitro in the mouse uterus and their regulation by ovarian steroid hormones. The expression of interleukin-1 beta (IL-1 beta), IL-1 alpha, IL-6, and tumor necrosis factor-alpha (TNF alpha) genes was examined in the mouse uterus as well as in freshly isolated or cultured epithelial cells by Northern blot and in situ hybridization. In the day 1 pregnant (D1 = vaginal plug) uterus, the levels of IL-1 alpha and IL-1 beta messenger RNAs (mRNAs) were abundant, whereas those of TNF alpha and IL-6 were at the limits of detection. Freshly isolated D1 uterine epithelial cell preparations contained higher levels of IL-1 alpha and IL-1 beta mRNAs than those observed in the D1 whole uterus, whereas TNF alpha and IL-6 mRNA levels were consistently low. In contrast, D1 epithelial cells showed decreased levels of IL-1 beta mRNA after 1 day of culture, whereas the levels of IL-1 alpha and IL-6 mRNAs increased under similar conditions. The levels of IL-1, IL-6, and TNF alpha mRNAs were at the limits of detection in the D4 whole uterus or freshly isolated diestrous epithelial cells. However, IL-1 alpha and IL-6 mRNA levels in diestrous epithelial cells, like those in D1 epithelial cells, increased in culture. In contrast, IL-1 beta and TNF alpha mRNA levels remained low in cultured epithelial cells. In situ hybridization was used to examine the cell type-specific expression of IL-1 alpha or IL-6 mRNA in uterine sections and cultured cells. Although hybridization signals for IL-1 alpha mRNA were detected in uterine epithelial cells on D1 of pregnancy, IL-6 mRNA could not be detected. IL-1 alpha and IL-6 mRNAs could not be detected in freshly isolated diestrous epithelial cells, although a majority of the epithelial cells showed hybridization signals for these mRNAs after 2 or 4 days of culture. The effects of steroid hormones on uterine cytokine gene expression were examined by Northern blot and in situ hybridization. In adult ovariectomized mice, an injection of 17 beta-estradiol (E2), progesterone (P4), or a combination of E2 and P4 had little or no apparent effect on these cytokine mRNA levels. The results establish that uterine epithelial cells on D1 of pregnancy exhibit heightened expression of IL-1 alpha in culture. In contrast, these cells express little or no IL-6 mRNA in vivo, but show heightened expression in culture. These results suggest that an apparent loss of repression of these uterine genes occurs in culture. Furthermore, E2 and/or P4 treatments appear to have little or no effect on uterine cytokine mRNA levels in adult ovariectomized mice.

摘要

本研究检测了小鼠子宫中细胞因子基因在体内和体外的差异表达及其受卵巢甾体激素的调控。通过Northern印迹法和原位杂交技术,检测了白细胞介素-1β(IL-1β)、IL-1α、IL-6和肿瘤坏死因子-α(TNFα)基因在小鼠子宫以及新鲜分离或培养的上皮细胞中的表达。在妊娠第1天(D1 = 阴道栓)的子宫中,IL-1α和IL-1β信使核糖核酸(mRNA)水平丰富,而TNFα和IL-6的水平处于检测极限。新鲜分离的D1子宫上皮细胞制剂中IL-1α和IL-1β mRNA的水平高于D1整个子宫中的水平,而TNFα和IL-6 mRNA水平一直较低。相反,D1上皮细胞培养1天后IL-1β mRNA水平下降,而在类似条件下IL-1α和IL-6 mRNA水平升高。在D4整个子宫或新鲜分离的动情期上皮细胞中,IL-1、IL-6和TNFα mRNA水平处于检测极限。然而,动情期上皮细胞中的IL-1α和IL-6 mRNA水平,与D1上皮细胞中的一样,在培养中升高。相反,培养的上皮细胞中IL-1β和TNFα mRNA水平仍然较低。原位杂交用于检测子宫切片和培养细胞中IL-1α或IL-6 mRNA的细胞类型特异性表达。虽然在妊娠第1天的子宫上皮细胞中检测到了IL-1α mRNA的杂交信号,但未检测到IL-6 mRNA。在新鲜分离的动情期上皮细胞中未检测到IL-1α和IL-6 mRNA,尽管大多数上皮细胞在培养2或4天后显示出这些mRNA的杂交信号。通过Northern印迹法和原位杂交技术检测了甾体激素对子宫细胞因子基因表达的影响。在成年去卵巢小鼠中,注射17β-雌二醇(E2)、孕酮(P4)或E2与P4的组合对这些细胞因子mRNA水平几乎没有或没有明显影响。结果表明,妊娠第1天的子宫上皮细胞在培养中IL-1α表达增强。相反,这些细胞在体内几乎不表达或不表达IL-6 mRNA,但在培养中表达增强。这些结果表明,这些子宫基因在培养中明显失去了抑制作用。此外,E2和/或P4处理对成年去卵巢小鼠的子宫细胞因子mRNA水平似乎几乎没有或没有影响。

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