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出生后发育阶段大鼠肠道中的细胞因子基因表达:断奶时白细胞介素-1表达增加。

Cytokine gene expression in intestine of rat during the postnatal developmental period: increased IL-1 expression at weaning.

作者信息

Mengheri E, Ciapponi L, Vignolini F, Nobili F

机构信息

Istituto Nazionale della Nutrizione, Roma, Italy.

出版信息

Life Sci. 1996;59(15):1227-36. doi: 10.1016/0024-3205(96)00446-8.

DOI:10.1016/0024-3205(96)00446-8
PMID:8845009
Abstract

In the present study we have investigate whether cytokines are constitutively and differently expressed in intestine during the differentiative processes that take place at weaning. We have analyzed the expression of IL-1 beta, IL-2, IL-4 and IFN gamma by polymerase chain reaction in Peyer's patches (PP) and in intestine deprived of PP (I-PP) of rats from 16 to 30 days of age. The results showed a constitutive and marked expression of the cytokines already before weaning, with the exception of IL-2 in PP and IFN gamma in I-PP. IL-beta was the only cytokine to show a different expression at various ages with an initial increase at 19 days and a further elevation at 21 days when intestinal epithelium passes through major differentiative stages, suggesting an involvement of this cytokine in intestinal development. We have also tested whether treatment of rats with the immunosuppressor cyclosporin A (CsA) could affect intestinal differentiation. The results showed that only some markers of differentiation were affected (proliferation of staminal crypt cells and length of crypts). This was probably due to a direct effect rather than an immunomediated effect of CsA, since treatment of three intestinal cell lines (Caco-2, HT-29, FRIC) with CsA indicated that this drug can exert a cytostatic activity on intestinal cells.

摘要

在本研究中,我们调查了在断奶时发生的分化过程中,细胞因子在肠道中是否组成性且差异性表达。我们通过聚合酶链反应分析了16至30日龄大鼠的派尔集合淋巴结(PP)和去除PP的肠道(I-PP)中IL-1β、IL-2、IL-4和IFNγ的表达。结果显示,在断奶前细胞因子就有组成性且显著的表达,但PP中的IL-2和I-PP中的IFNγ除外。IL-β是唯一在不同年龄表现出差异表达的细胞因子,在19天时最初升高,在21天时进一步升高,此时肠道上皮细胞经历主要的分化阶段,提示该细胞因子参与肠道发育。我们还测试了用免疫抑制剂环孢素A(CsA)处理大鼠是否会影响肠道分化。结果表明,只有一些分化标志物受到影响(干细胞隐窝细胞的增殖和隐窝长度)。这可能是由于CsA的直接作用而非免疫介导作用,因为用CsA处理三种肠道细胞系(Caco-2、HT-29、FRIC)表明该药物可对肠道细胞发挥细胞生长抑制活性。

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