Erjefält J S, Erjefält I, Sundler F, Persson C G
Department of Medical Cell Research, University of Lund, Sweden.
Cell Tissue Res. 1995 Aug;281(2):305-16. doi: 10.1007/BF00583399.
Epithelial shedding occurs in health and, extensively, in inflammatory airway diseases. This study describes deepithelialisation, reepithelialisation and associated events in guinea-pig trachea after shedding-like epithelial denudation in vivo. Mechanical deepithelialisation of an 800-microns wide tracheal zone was carried out using an orotracheal steel probe without bleeding or damage to the basement membrane. Reepithelialisation was studied by scanning- and transmission electron microscopy and light microscopy. Nerve fibres were examined by immunostaining. Cell proliferation was analysed by [3H]-thymidine autoradiography. Immediately after epithelial removal secretory and ciliated (and presumably basal) epithelial cells at the wound margin dedifferentiated, flattened and migrated rapidly (2-3 microns/min) over the denuded basement membrane. Within 8-15 h a new, flattened epithelium covered the entire deepithelialised zone. At 30 h a tight epithelial barrier was established and after 5 days the epithelium was fully redifferentiated. After completed migration an increased mitotic activity occurred in the epithelium and in fibroblasts/smooth muscle beneath the restitution zone. Reinnervating intraepithelial calcitonin gene-related peptide-containing nerve fibres appeared within 30 h. We conclude that (1) reproducible shedding-like denudation, without bleeding or damage to the basement membrane, can be produced in vivo; (2) secretory and ciliated cells participate in reepithelialisation by dedifferentiation and migration; (3) the initial migration is very fast in vivo; (4) shedding-like denudation may cause strong secretory and exudative responses as well as proliferation of epithelium, and fibroblasts/smooth muscle. Rapid restitution of airway epithelium may depend on contributions from the microcirculation and innervation.
上皮脱落现象在健康状态下会出现,在炎症性气道疾病中更是广泛存在。本研究描述了豚鼠气管在体内发生类似脱落的上皮剥脱后再上皮化及相关事件。使用经口气管钢探针在一个800微米宽的气管区域进行机械性上皮剥脱,未出现出血或基底膜损伤。通过扫描电子显微镜、透射电子显微镜和光学显微镜研究再上皮化过程。通过免疫染色检查神经纤维。利用[³H] - 胸腺嘧啶核苷放射自显影分析细胞增殖。上皮去除后,伤口边缘的分泌性、纤毛(可能还有基底)上皮细胞立即去分化、变扁平并在裸露的基底膜上快速迁移(2 - 3微米/分钟)。在8 - 15小时内,一个新的扁平上皮覆盖了整个上皮剥脱区域。30小时时建立了紧密的上皮屏障,5天后上皮完全重新分化。迁移完成后,上皮以及修复区域下方的成纤维细胞/平滑肌中出现有丝分裂活性增加。含降钙素基因相关肽的再支配上皮内神经纤维在30小时内出现。我们得出结论:(1)在体内可产生可重复的类似脱落的剥脱,且不出血或不损伤基底膜;(2)分泌性和纤毛细胞通过去分化和迁移参与再上皮化;(3)体内初始迁移非常迅速;(4)类似脱落的剥脱可能引发强烈的分泌和渗出反应以及上皮、成纤维细胞和平滑肌的增殖。气道上皮的快速修复可能依赖于微循环和神经支配的作用。