Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Medical Biochemistry and Cell Biology, University of Gothenburg, Gothenburg, Sweden.
Am J Respir Crit Care Med. 2022 Nov 1;206(9):1081-1095. doi: 10.1164/rccm.202202-0309OC.
MUC5AC (mucin 5AC, oligomeric gel-forming) and MUC5B (mucin 5B, oligomeric gel-forming) are the predominant secreted polymeric mucins in mammalian airways. They contribute differently to the pathogenesis of various muco-obstructive and interstitial lung diseases, and their genes are separately regulated, but whether they are packaged together or in separate secretory granules is not known. To determine the packaging of MUC5AC and MUC5B within individual secretory granules in mouse and human airways under varying conditions of inflammation and along the proximal-distal axis. Lung tissue was obtained from mice stimulated to upregulate mucin production by the cytokines IL-1 and IL-13 or by porcine pancreatic elastase. Human lung tissue was obtained from donated normal lungs, biopsy samples of transplanted lungs, and explanted lungs from subjects with chronic obstructive pulmonary disease. MUC5AC and MUC5B were labeled with antibodies from different animal species or, in mice only, by transgenic chimeric mucin-fluorescent proteins and imaged using widefield deconvolution or Airyscan fluorescence microscopy. In both mouse and human airways, most secretory granules contained both mucins interdigitating within the granules. Smaller numbers of granules contained MUC5B alone, and even fewer contained MUC5AC alone. MUC5AC and MUC5B are variably stored both in the same and in separate secretory granules of both mice and humans. The high fraction of granules containing both mucins under a variety of conditions makes it unlikely that their secretion can be differentially controlled as a therapeutic strategy. This work also advances knowledge of the packaging of mucins within secretory granules to understand mechanisms of epithelial stress in the pathogenesis of chronic lung diseases.
黏蛋白 5AC(黏蛋白 5AC,寡聚凝胶形成)和黏蛋白 5B(黏蛋白 5B,寡聚凝胶形成)是哺乳动物气道中主要的分泌性聚合黏蛋白。它们在各种黏液阻塞性和间质性肺疾病的发病机制中发挥不同的作用,其基因分别受到调控,但它们是否被包装在一起或在单独的分泌颗粒中尚不清楚。本研究旨在确定在不同炎症条件下和沿近-远轴,在小鼠和人呼吸道中,MUC5AC 和 MUC5B 在单个分泌颗粒中的包装情况。通过细胞因子 IL-1 和 IL-13 或猪胰弹性蛋白酶刺激小鼠,获得肺组织,以增加黏蛋白的产生。从捐赠的正常肺、移植肺活检样本和慢性阻塞性肺疾病患者的离体肺中获取人肺组织。用来自不同动物物种的抗体或仅在小鼠中用转基因嵌合黏蛋白-荧光蛋白标记 MUC5AC 和 MUC5B,并使用宽场去卷积或 Airyscan 荧光显微镜进行成像。在小鼠和人呼吸道中,大多数分泌颗粒内都有两种黏蛋白相互交织。少数颗粒内仅含有 MUC5B,甚至更少的颗粒内仅含有 MUC5AC。MUC5AC 和 MUC5B 可在不同条件下以相同或不同的分泌颗粒中进行可变储存。在各种条件下,含有两种黏蛋白的颗粒比例很高,使得作为一种治疗策略,很难对它们的分泌进行差异控制。这项工作还增进了对黏蛋白在分泌颗粒内包装的认识,以了解慢性肺部疾病发病机制中上皮应激的机制。