Váradi Judit, Harazin András, Fenyvesi Ferenc, Réti-Nagy Katalin, Gogolák Péter, Vámosi György, Bácskay Ildikó, Fehér Pálma, Ujhelyi Zoltán, Vasvári Gábor, Róka Eszter, Haines David, Deli Mária A, Vecsernyés Miklós
Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, Debrecen, Hungary.
Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
PLoS One. 2017 Jan 19;12(1):e0170537. doi: 10.1371/journal.pone.0170537. eCollection 2017.
Alpha-melanocyte-stimulating hormone (α-MSH) is a potent anti-inflammatory peptide with cytoprotective effect in various tissues. The present investigation demonstrates the ability of α-MSH to interact with intestinal epithelial cell monolayers and mitigate inflammatory processes of the epithelial barrier. The protective effect of α-MSH was studied on Caco-2 human intestinal epithelial monolayers, which were disrupted by exposure to tumor necrosis factor-α and interleukin-1β. The barrier integrity was assessed by measuring transepithelial electric resistance (TEER) and permeability for marker molecules. Caco-2 monolayers were evaluated by immunohistochemistry for expression of melanocortin-1 receptor and tight junction proteins ZO-1 and claudin-4. The activation of nuclear factor kappa beta (NF-κB) was detected by fluorescence microscopy and inflammatory cytokine expression was assessed by flow cytometric bead array cytokine assay. Exposure of Caco-2 monolayers to proinflammatory cytokines lowered TEER and increased permeability for fluorescein and albumin, which was accompanied by changes in ZO-1 and claudin-4 immunostaining. α-MSH was able to prevent inflammation-associated decrease of TEER in a dose-dependent manner and reduce the increased permeability for paracellular marker fluorescein. Further immunohistochemistry analysis revealed proinflammatory cytokine induced translocation of the NF-κB p65 subunit into Caco-2 cell nuclei, which was inhibited by α-MSH. As a result the IL-6 and IL-8 production of Caco-2 monolayers were also decreased with different patterns by the addition of α-MSH to the culture medium. In conclusion, Caco-2 cells showed a positive immunostaining for melanocortin-1 receptor and α-MSH protected Caco-2 cells against inflammatory barrier dysfunction and inflammatory activation induced by tumor necrosis factor-α and interleukin-1β cytokines.
α-黑素细胞刺激素(α-MSH)是一种具有强大抗炎作用的肽,在多种组织中具有细胞保护作用。本研究证明了α-MSH与肠上皮细胞单层相互作用并减轻上皮屏障炎症过程的能力。研究了α-MSH对Caco-2人肠上皮单层的保护作用,该单层因暴露于肿瘤坏死因子-α和白细胞介素-1β而被破坏。通过测量跨上皮电阻(TEER)和标记分子的通透性来评估屏障完整性。通过免疫组织化学评估Caco-2单层中黑素皮质素-1受体以及紧密连接蛋白ZO-1和claudin-4的表达。通过荧光显微镜检测核因子κB(NF-κB)的激活,并通过流式细胞术磁珠阵列细胞因子测定法评估炎性细胞因子的表达。将Caco-2单层暴露于促炎细胞因子会降低TEER,并增加荧光素和白蛋白的通透性,同时伴有ZO-1和claudin-4免疫染色的变化。α-MSH能够以剂量依赖性方式预防与炎症相关的TEER降低,并降低细胞旁标记物荧光素增加的通透性。进一步的免疫组织化学分析显示,促炎细胞因子诱导NF-κB p65亚基易位到Caco-2细胞核中,而α-MSH可抑制这种易位。结果,通过向培养基中添加α-MSH,Caco-2单层的IL-6和IL-8产生也以不同模式减少。总之,Caco-2细胞对黑素皮质素-1受体呈阳性免疫染色,α-MSH保护Caco-2细胞免受肿瘤坏死因子-α和白细胞介素-1β细胞因子诱导的炎症屏障功能障碍和炎症激活。