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Myofibroblast keratinocyte growth factor reduces tight junctional integrity and increases claudin-2 levels in polarized Caco-2 cells

机译:myOfbroblast角蛋白细胞生长因子降低了偏极性Caco-2细胞中的紧密连接完整性并增加了克劳德蛋白-2水平

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摘要

The colonic epithelium is composed of a polarized monolayer sheathed by a layer of pericryptal myofibroblasts (PCMFs). We mimicked these cellular compartments in vitro to assess the effects of paracrine-acting PCMF-derived factors on tight junction (TJ) integrity, as measured by transepithelial electrical resistance (TER). Co-culture with 18Co PCMFs, or basolateral administration of 18Co conditioned medium (CM), significantly reduced TER of polarized Caco-2 cells. Amongst candidate paracrine factors, only keratinocyte growth factor (KGF) reduced Caco-2 TER; basolateral KGF treatment led to time- and concentration-dependent increases in claudin-2 levels. We also demonstrate amphiregulin (AREG), produced largely by Caco-2 cells, increased claudin-2 levels, leading to epidermal growth factor receptor-mediated TER reduction. We propose that colonic epithelial TJ integrity can be modulated by paracrine KGF and autocrine AREG through increased claudin-2 levels. KGF-regulated claudin-2 induction may have implications for inflammatory bowel disease, where both KGF and claudin-2 are upregulated.
机译:结肠上皮由极化的单层细胞组成,该细胞膜被一层隐膜成肌纤维细胞(PCMF)包裹。我们在体外模拟了这些细胞区室,以评估旁分泌作用的PCMF衍生因子对紧密连接(TJ)完整性的影响,通过跨上皮电阻(TER)进行测量。与18Co PCMFs共培养,或18Co条件培养基(CM)的基底外侧给药,可显着降低极化Caco-2细胞的TER。在候选旁分泌因子中,只有角质形成细胞生长因子(KGF)降低了Caco-2 TER。基底外侧KGF治疗导致claudin-2水平的时间依赖性和浓度依赖性增加。我们还演示了主要由Caco-2细胞产生的双调蛋白(AREG),增加了claudin-2的水平,导致表皮生长因子受体介导的TER降低。我们建议结肠旁上皮TJ完整性可以通过增加claudin-2水平由旁分泌KGF和自分泌AREG调节。 KGF调节的claudin-2诱导可能与炎症性肠病有关,KGF和claudin-2均被上调。

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