Woods Lucas T, Camden Jean M, El-Sayed Farid G, Khalafalla Mahmoud G, Petris Michael J, Erb Laurie, Weisman Gary A
Department of Biochemistry, University of Missouri, Columbia, Missouri, United States of America; Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri, United States of America.
Department of Biochemistry, University of Missouri, Columbia, Missouri, United States of America; Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri, United States of America; Department of Nutritional Sciences and Exercise Physiology, University of Missouri, Columbia, Missouri, United States of America.
PLoS One. 2015 May 8;10(5):e0123641. doi: 10.1371/journal.pone.0123641. eCollection 2015.
Transforming growth factor-β (TGF-β) is a multi-functional cytokine with a well-described role in the regulation of tissue fibrosis and regeneration in the liver, kidney and lung. Submandibular gland (SMG) duct ligation and subsequent deligation in rodents is a classical model for studying salivary gland damage and regeneration. While previous studies suggest that TGF-β may contribute to salivary gland fibrosis, the expression of TGF-β signaling components has not been investigated in relation to mouse SMG duct ligation-induced fibrosis and regeneration following ductal deligation. Following a 7 day SMG duct ligation, TGF-β1 and TGF-β3 were significantly upregulated in the SMG, as were TGF-β receptor 1 and downstream Smad family transcription factors in salivary acinar cells, but not in ductal cells. In acinar cells, duct ligation also led to upregulation of snail, a Smad-activated E-cadherin repressor and regulator of epithelial-mesenchymal transition, whereas in ductal cells upregulation of E-cadherin was observed while snail expression was unchanged. Upregulation of these TGF-β signaling components correlated with upregulation of fibrosis markers collagen 1 and fibronectin, responses that were inhibited by administration of the TGF-β receptor 1 inhibitors SB431542 or GW788388. After SMG regeneration following a 28 day duct deligation, TGF-β signaling components and epithelial-mesenchymal transition markers returned to levels similar to non-ligated controls. The results from this study indicate that increased TGF-β signaling contributes to duct ligation-induced changes in salivary epithelium that correlate with glandular fibrosis. Furthermore, the reversibility of enhanced TGF-β signaling in acinar cells of duct-ligated mouse SMG after deligation indicates that this is an ideal model for studying TGF-β signaling mechanisms in salivary epithelium as well as mechanisms of fibrosis initiation and their resolution.
转化生长因子-β(TGF-β)是一种多功能细胞因子,在肝脏、肾脏和肺的组织纤维化及再生调节中具有明确作用。啮齿动物的下颌下腺(SMG)导管结扎及随后的松解是研究唾液腺损伤和再生的经典模型。虽然先前的研究表明TGF-β可能促成唾液腺纤维化,但尚未针对小鼠SMG导管结扎诱导的纤维化以及导管松解后的再生情况,研究TGF-β信号传导成分的表达。在进行7天的SMG导管结扎后,SMG中TGF-β1和TGF-β3显著上调,唾液腺泡细胞中的TGF-β受体1及下游Smad家族转录因子也是如此,但导管细胞中并非如此。在腺泡细胞中,导管结扎还导致蜗牛蛋白上调,蜗牛蛋白是一种Smad激活的E-钙黏蛋白抑制因子及上皮-间质转化调节因子,而在导管细胞中观察到E-钙黏蛋白上调,蜗牛蛋白表达未变。这些TGF-β信号传导成分的上调与纤维化标志物胶原蛋白1和纤连蛋白的上调相关,给予TGF-β受体1抑制剂SB431542或GW788388可抑制这些反应。在28天导管松解后的SMG再生后,TGF-β信号传导成分和上皮-间质转化标志物恢复到与未结扎对照相似的水平。本研究结果表明,TGF-β信号增强促成了导管结扎诱导的唾液上皮变化,这与腺体纤维化相关。此外,导管结扎小鼠SMG腺泡细胞中增强的TGF-β信号在松解后具有可逆性,这表明这是研究唾液上皮中TGF-β信号传导机制以及纤维化起始及其消退机制的理想模型。