Department of Medical Biochemistry, Institute of Biomedicine, University of Gothenburg, 40530 Gothenburg, Sweden.
Department of Veterinary Pathology, Freie Universität Berlin, Germany.
EBioMedicine. 2018 Jul;33:134-143. doi: 10.1016/j.ebiom.2018.05.031. Epub 2018 Jun 7.
Many epithelial surfaces of the body are covered with protective mucus, and disrupted mucus homeostasis is coupled to diseases such as ulcerative colitis, helminth infection, cystic fibrosis, and chronic obstructive lung disease. However, little is known how a balanced mucus system is maintained. By investigating the involvement of proteases in colonic mucus dynamics we identified metalloprotease activity to be a key contributor to mucus expansion. The effect was mediated by calcium-activated chloride channel regulator 1 (CLCA1) as application of recombinant CLCA1 on intestinal mucus in freshly dissected tissue resulted in increased mucus thickness independently of ion and mucus secretion, but dependent on its metallohydrolase activity. Further, CLCA1 modulated mucus dynamics in both human and mouse, and knock-out of CLCA1 in mice was compensated for by cysteine proteases. Our results suggest that CLCA1 is involved in intestinal mucus homeostasis by facilitating processing and removal of mucus to prevent stagnation. In light of our findings, we suggest future studies to investigate if upregulation of CLCA1 in diseases associated with mucus accumulation could facilitate removal of mucus in an attempt to maintain homeostasis.
许多身体的上皮表面都覆盖着保护性黏液,黏液动态平衡的破坏与溃疡性结肠炎、寄生虫感染、囊性纤维化和慢性阻塞性肺病等疾病有关。然而,人们对如何维持平衡的黏液系统知之甚少。通过研究蛋白酶在结肠黏液动力学中的作用,我们发现金属蛋白酶活性是黏液扩张的关键因素。这种作用是通过钙激活氯离子通道调节剂 1(CLCA1)介导的,因为将重组 CLCA1 应用于新鲜分离组织中的肠黏液会导致黏液厚度增加,这与离子和黏液分泌无关,而是依赖于其金属水解酶活性。此外,CLCA1 调节了人和小鼠的黏液动力学,并且小鼠中 CLCA1 的敲除被半胱氨酸蛋白酶所补偿。我们的研究结果表明,CLCA1 通过促进黏液的加工和清除来参与肠道黏液动态平衡,以防止停滞。鉴于我们的发现,我们建议未来的研究调查在与黏液积累相关的疾病中上调 CLCA1 是否可以促进黏液的清除,以试图维持动态平衡。