缝隙连接
细胞生物学
免疫标记
细胞内
细胞结
肺泡上皮
连接蛋白
肺
巨噬细胞
病理
紧密连接
生物
细胞
化学
上皮
肺泡巨噬细胞
免疫学
医学
体外
免疫组织化学
内科学
生物化学
遗传学
作者
Anja Beckmann,Alexander Grißmer,Carola Meier,Thomas Tschernig
标识
DOI:10.1016/j.aanat.2019.151417
摘要
Abstract Background The alveolus in the lung tissue is an extremely vulnerable site. Alveolar macrophages control this micro-environment both in states of health and illnesssuch as acute lung injury and infection. It has been reported in mice in vivo that intercellular communication between alveolar macrophages and alveolar epithelial cells is mediated by gap junctions. However, little is known about thismicro-environment in human cells. Methods Since this gap junctional intercellular communication is hard to investigate in human tissues, a co-culture model of two human cell lines, one of epithelial and one of macrophage origin, was used. Immunoblot analysis, freeze fracture replica immunolabeling and electron microscopy were performed. Results Connexin (Cx) 43 protein expression as well as ultrastructurally defined Cx43 gap junctions were detected in co-cultures, yielding evidence of intercellular gap junctions between human alveolar cells of two distinct entities. Conclusion Alveolar macrophages possibly have direct access to the alveolar epithelium via gap junctions in humans, enabling the orchestration of the microenvironment in physiology and disease states.
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