Lin You-Min, Li Feng, Shi Xuan-Zheng
Division of Gastroenterology, Department of Internal Medicine, The University of Texas Medical Branch, Galveston, Texas, United States of America.
PLoS One. 2014 Sep 2;9(9):e106242. doi: 10.1371/journal.pone.0106242. eCollection 2014.
Inflammatory infiltrates and pro-inflammatory mediators are found increased in obstructive and functional bowel disorders, in which lumen distention is present. However, what caused the low level inflammation is not well known. We tested the hypothesis that lumen distention- associated mechanical stress may induce expression of specific inflammatory mediators in gut smooth muscle.
Static mechanical stretch (18% elongation) was applied in vitro in primary culture of rat colonic circular smooth muscle cells (RCCSMCs) with a Flexercell FX-4000 Tension Plus System. Mechanical distention in vivo was induced in rats with an obstruction band placed in the distal colon.
In the primary culture of RCCSMCs, we found that static stretch significantly induced mRNA expression of iNOS, IL-6, and MCP-1 in 3 hours by 6.0(±1.4), 2.5(±0.5), and 2.2(±0.5) fold (n = 6∼8, p<0.05), respectively. However, gene expression of TNF-α, IL-1β, and IL-8 was not significantly affected by mechanical stretch. In the in vivo model of colon obstruction, we found that gene expression of iNOS, IL-6, and MCP-1 is also significantly increased in a time-dependent manner in the mechanically distended proximal segment, but not in the sham controls or distal segments. The conditioned medium from the muscle strips of the stretched proximal segment, but not the distal segment or control, significantly induced translocation and phosphorylation of NF-κB p65. This treatment further increased mRNA expression of inflammatory mediators in the naïve cells. However, treatment of the conditioned medium from the proximal segment with neutralizing antibody against rat IL-6 significantly attenuated the activation of NF-κB and gene expression of inflammatory mediators.
Our studies demonstrate that mechanical stress induces gene expression of inflammatory mediators i.e. iNOS, IL-6, and MCP-1 in colonic SMC. Further ex vivo study showed that mechanical stress functions as a pro-inflammatory stimulus in the gut.
在存在肠腔扩张的阻塞性和功能性肠病中发现炎症浸润和促炎介质增加。然而,导致低水平炎症的原因尚不清楚。我们检验了这样一个假设,即与肠腔扩张相关的机械应力可能诱导肠道平滑肌中特定炎症介质的表达。
使用Flexercell FX - 4000张力增强系统在体外对大鼠结肠环行平滑肌细胞(RCCSMCs)原代培养物施加静态机械拉伸(18%伸长)。通过在大鼠远端结肠放置阻塞带在体内诱导机械扩张。
在RCCSMCs原代培养物中,我们发现静态拉伸在3小时内显著诱导诱导型一氧化氮合酶(iNOS)、白细胞介素 - 6(IL - 6)和单核细胞趋化蛋白 - 1(MCP - 1)的mRNA表达分别增加6.0(±1.4)、2.5(±0.5)和2.2(±0.5)倍(n = 6 - 8,p < 0.05)。然而,肿瘤坏死因子 - α(TNF - α)、白细胞介素 - 1β(IL - 1β)和白细胞介素 - 8(IL - 8)的基因表达未受到机械拉伸的显著影响。在结肠梗阻的体内模型中,我们发现iNOS、IL - 6和MCP - 1的基因表达在机械扩张的近端段也以时间依赖性方式显著增加,但在假手术对照组或远端段未增加。来自拉伸近端段肌肉条的条件培养基,但不是远端段或对照组的,显著诱导核因子κB p65(NF - κB p65)的易位和磷酸化。这种处理进一步增加了未处理细胞中炎症介质的mRNA表达。然而,用抗大鼠IL - 6中和抗体处理近端段的条件培养基显著减弱了NF - κB的激活和炎症介质的基因表达。
我们的研究表明机械应力诱导结肠平滑肌中炎症介质即iNOS、IL - 6和MCP - 1的基因表达。进一步的体外研究表明机械应力在肠道中起促炎刺激作用。