Eenjes Evelien, Tibboel Dick, Wijnen Rene M H, Rottier Robbert J
Department of Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, Rotterdam, Netherlands.
Department of Cell Biology, Erasmus MC, Rotterdam, Netherlands.
Front Cell Dev Biol. 2022 Oct 10;10:1022457. doi: 10.3389/fcell.2022.1022457. eCollection 2022.
The lung is composed of a highly branched airway structure, which humidifies and warms the inhaled air before entering the alveolar compartment. In the alveoli, a thin layer of epithelium is in close proximity with the capillary endothelium, allowing for an efficient exchange of oxygen and carbon dioxide. During development proliferation and differentiation of progenitor cells generates the lung architecture, and in the adult lung a proper function of progenitor cells is needed to regenerate after injury. Malfunctioning of progenitors during development results in various congenital lung disorders, such as Congenital Diaphragmatic Hernia (CDH) and Congenital Pulmonary Adenomatoid Malformation (CPAM). In addition, many premature neonates experience continuous insults on the lung caused by artificial ventilation and supplemental oxygen, which requires a highly controlled mechanism of airway repair. Malfunctioning of airway progenitors during regeneration can result in reduction of respiratory function or (chronic) airway diseases. Pathways that are active during development are frequently re-activated upon damage. Understanding the basic mechanisms of lung development and the behavior of progenitor cell in the ontogeny and regeneration of the lung may help to better understand the underlying cause of lung diseases, especially those occurring in prenatal development or in the immediate postnatal period of life. This review provides an overview of lung development and the cell types involved in repair of lung damage with a focus on the airway.
肺由高度分支的气道结构组成,该结构在吸入空气进入肺泡腔之前对其进行加湿和加热。在肺泡中,一层薄薄的上皮细胞与毛细血管内皮紧密相邻,使得氧气和二氧化碳能够高效交换。在发育过程中,祖细胞的增殖和分化产生了肺的结构,而在成年肺中,损伤后需要祖细胞发挥正常功能来实现再生。发育过程中祖细胞功能失调会导致各种先天性肺部疾病,如先天性膈疝(CDH)和先天性肺腺瘤样畸形(CPAM)。此外,许多早产儿会因人工通气和补充氧气而持续遭受肺部损伤,这需要高度可控的气道修复机制。再生过程中气道祖细胞功能失调会导致呼吸功能下降或引发(慢性)气道疾病。发育过程中活跃的信号通路在损伤时常常会重新激活。了解肺发育的基本机制以及祖细胞在肺个体发育和再生中的行为,可能有助于更好地理解肺部疾病的潜在病因,尤其是那些发生在产前发育阶段或生命早期新生儿期的疾病。本综述概述了肺发育以及参与肺损伤修复的细胞类型,重点关注气道。