人肺肺泡细胞复合体的超微结构及其功能相关性研究进展

Vasudha Kulkarni, H. Tejaswi, Ashwini C. Appaji
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引用次数: 0

摘要

人的肺是一个不断生物转化的动态器官。在40种不同的肺细胞类型中,1型和2型肺细胞、肺毛细血管内皮和肺间质细胞在肺功能中发挥着至关重要的作用。探索这些细胞的结构将有助于阐明影响肺部的各种疾病的发病机制。使用Medline、Google Scholar和Cochrane三个研究数据库进行了系统的文献检索。在1981年至2020年间发表的90篇文章中,根据纳入和排除标准,有41篇文章被纳入研究。在肺肺泡细胞复合体的细胞成分中,2型肺细胞在表面活性剂合成、免疫反应和再生能力方面表现出多功能性。肺损伤的发病机制是由于2型肺细胞功能的丧失和细胞间连接功能的差异。无论肺部疾病的原因如何,肺泡毛细血管膜的通透性都会增加,从而导致间质水肿。这反过来又会导致换气过度、血氧饱和度低和肺活量下降。存在于间质中的周细胞对肺损伤和潜在的干细胞功能具有预防作用。关键词:肺泡上皮细胞、毛细血管内皮、肺间质、1型肺细胞、2型肺细胞
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Ultrastructure of the Alveolar Cell Complex of Human Lung and its Functional Correlation: A Review
The human lung is a dynamic organ of constant biotransformation. Out of 40 different cell types of lungs, Type‑1 and Type‑2 pneumocytes, pulmonary capillary endothelium, and cells of lung interstitium play a vital role in functioning of the lung. Exploring the structure of these cells would shed light on the pathogenesis of various diseases affecting the lungs. A systematic literature search was conducted using three research databases – Medline, Google Scholar, and Cochrane. Out of ninety articles published between the year 1981 and 2020, 41 articles were included in the study based on the inclusion and exclusion criteria. Among the cellular components of the alveolar cell complex of the lung, the Type‑2 pneumocytes show versatility in its function in the form of surfactant synthesis, immune reaction, and regenerative capacity. The pathogenesis of the lung injury is due to the loss of functions of the Type‑2 pneumocytes and the intercellular junction functional discrepancy. Irrespective of the cause of lung disease, there is an increase in permeability in the alveolocapillary membrane leading to interstitial edema. This, in turn, leads to hyperventilation, low oxygen saturation, and a decrease in lung capacity. The pericytes present in the interstitium have a preventive role to play in lung injury and potential stem cell function. Keywords: alveolar epithelial cells, capillary endothelium, lung interstitium, type-1 pneumocytes, type-2 pneumocytes
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