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白细胞介素-1、白细胞介素-8、肿瘤坏死因子α和干扰素γ可刺激小肠细胞系中的DNA合成,但对细胞凋亡无影响。

Interleukin-1, interleukin-8, tumour necrosis factor alpha and interferon gamma stimulate DNA synthesis but have no effect on apoptosis in small-intestinal cell lines.

作者信息

Zachrisson K, Neopikhanov V, Samali A, Uribe A

机构信息

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

出版信息

Eur J Gastroenterol Hepatol. 2001 May;13(5):551-9. doi: 10.1097/00042737-200105000-00015.

Abstract

OBJECTIVES

Cytokines stimulate lymphocyte cell proliferation and affect cell division in several other cell types. Helicobacter pylori-induced gastritis and coeliac disease are characterized by an increased cell proliferation in association with an increased production of proinflammatory cytokines, which could contribute to these cell kinetic changes. Our aim is to examine in vitro whether cytokines usually present in the gastrointestinal mucosa affect DNA synthesis and apoptosis in a rat and a human small-intestinal cell line.

METHODS

IEC-6 and FHs-74 cells were incubated for 24 h with 10(-13)-10(-9) M of tumour necrosis factor alpha (TNF-alpha), interleukin-1beta (IL-1beta), interleukin-2 (IL-2), interleukin-6 (IL-6), interleukin-8 (IL-8), transforming growth factor-beta (TGF-beta) and interferon gamma (IFN-gamma). IEC-6 cells were also incubated with 10(-13)-10(-9) M of interleukin-1alpha (IL-1alpha) and 10(-8) M of interleukin-1 receptor antagonist (IL-1ra). The cells were labelled with 3H-methyl thymidine for the final 4 hours, and then processed for autoradiography. DNA synthesis was evaluated by the labelling index (LI%). Apoptosis was evaluated in IEC-6 cells by changes in membrane lipid asymmetry using annexin-V binding to externalized phosphatidylserine (flow cytometry) and by estimating the caspase activity.

RESULTS

TNF-alpha, IL-1beta, IL-8 and IFN-gamma significantly and markedly increased the LI, even at low concentrations (P< 0.0001), in both IEC-6 and FHs-74 cells, as did IL-1alpha in IEC-6 cells. TGF-beta significantly reduced the LI in both cell lines (P< 0.0001), whereas IL-2, IL-6 and IL-1ra did not affect DNA synthesis significantly. None of IL-1beta, IL-8, TNF-alpha or IFN-gamma affected apoptosis in IEC-6 cells.

CONCLUSION

TNF-alpha, IL-1alpha, IL-1beta, IL-8 and IFN-gamma stimulated DNA synthesis in a human and a rat small-intestinal cell line. The cytokines exert their mitogenic action directly on the intestinal cells via specific receptors. Our findings indicate that pro-inflammatory cytokines may participate in the regulation of the gastrointestinal epithelial cell proliferation in health and disease.

摘要

目的

细胞因子可刺激淋巴细胞增殖,并影响其他几种细胞类型的细胞分裂。幽门螺杆菌引起的胃炎和乳糜泻的特征是细胞增殖增加,同时促炎细胞因子的产生也增加,这可能导致这些细胞动力学变化。我们的目的是在体外研究胃肠道黏膜中通常存在的细胞因子是否会影响大鼠和人小肠细胞系中的DNA合成和细胞凋亡。

方法

将IEC-6和FHs-74细胞与10⁻¹³ - 10⁻⁹ M的肿瘤坏死因子α(TNF-α)、白细胞介素-1β(IL-1β)、白细胞介素-2(IL-2)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、转化生长因子-β(TGF-β)和干扰素γ(IFN-γ)孵育24小时。IEC-6细胞还与10⁻¹³ - 10⁻⁹ M的白细胞介素-1α(IL-1α)和10⁻⁸ M的白细胞介素-1受体拮抗剂(IL-1ra)孵育。在最后4小时用³H-甲基胸苷标记细胞,然后进行放射自显影处理。通过标记指数(LI%)评估DNA合成。通过膜联蛋白-V与外化磷脂酰丝氨酸结合(流式细胞术)以及通过估计半胱天冬酶活性来评估IEC-6细胞中的细胞凋亡。

结果

TNF-α、IL-1β、IL-8和IFN-γ即使在低浓度下(P < 0.0001)也能显著且明显增加IEC-6和FHs-74细胞中的LI,IEC-6细胞中的IL-1α也是如此。TGF-β显著降低了两种细胞系中的LI(P < 0.0001),而IL-2、IL-6和IL-1ra对DNA合成没有显著影响。IL-1β、IL-8、TNF-α或IFN-γ均未影响IEC-6细胞中的细胞凋亡。

结论

TNF-α、IL-1α、IL-1β、IL-8和IFN-γ刺激了人及大鼠小肠细胞系中的DNA合成。这些细胞因子通过特定受体直接对肠道细胞发挥促有丝分裂作用。我们的研究结果表明,促炎细胞因子可能参与健康和疾病状态下胃肠道上皮细胞增殖的调节。

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