Szoták-Ajtay Kitti, Szõke Dániel, Kovács Gábor, Andréka Judit, Brenner Gábor B, Giricz Zoltán, Penninger Josef, Kahn Mark L, Jakus Zoltán
Department of Physiology, Semmelweis University School of Medicine, Budapest, Hungary.
MTA-SE "Lendület" Lymphatic Physiology Research Group of the Hungarian Academy of Sciences and the Semmelweis University, Budapest, Hungary.
Front Bioeng Biotechnol. 2020 Mar 6;8:136. doi: 10.3389/fbioe.2020.00136. eCollection 2020.
Embryonic lungs must be inflated immediately after birth to establish respiration. In addition to pulmonary surfactant, recently, we have revealed lymphatic function as a previously unknown regulator of prenatal lung compliance that prepares the embryonic lung for inflation at birth. It is well-documented that the late gestation embryo performs episodic breathing-like movements called as fetal breathing movements (FBMs), but the physiological importance of these events is not clear. Here we aimed to study the physiological role of FBMs in preparation for air inflation at birth. late gestation embryos develop a progressive loss of spinal motor neurons associated with axonal degeneration and denervation of neuromuscular junctions serving as an ideal genetic model to test the possible role of FBMs. We demonstrated that newborns show impaired motor function resulting in fatal respiratory failure after birth. Next, we showed that the alveolar septa are thicker, and the alveolar area is reduced in late gestation embryos, while the expression of molecular markers of lung development are not affected. Importantly, pulmonary lymphatic vessels are dilated and the prenatal pulmonary lymphatic function is reduced in late gestation embryos. Our results have revealed that mice show impaired motor functions including FBMs, and late gestation embryos display reduced prenatal lymphatic function and impaired lung expansion represented as thickened alveolar septa and reduced alveolar area in preparation of the developing lung for inflation at birth. These findings suggest a possible mechanism that FBMs, similarly to breathing movements after birth, stimulate prenatal lymphatic function in pulmonary collecting lymphatics lacking smooth muscle coverage to prepare the developing lung for inflation and gas exchange at birth. Moreover, these results raise the possibility that stimulating FBMs during late gestation might be an effective way to reduce the risk of the development of neonatal respiratory failure.
胚胎肺在出生后必须立即充气以建立呼吸。除了肺表面活性物质外,最近我们还发现淋巴功能是一种先前未知的产前肺顺应性调节因子,它为胚胎肺在出生时充气做好准备。有充分的文献记载,妊娠晚期胚胎会进行类似呼吸的间歇性运动,称为胎儿呼吸运动(FBMs),但这些运动的生理重要性尚不清楚。在这里,我们旨在研究FBMs在为出生时空气充气做准备中的生理作用。妊娠晚期胚胎会出现与轴突退化和神经肌肉接头去神经支配相关的脊髓运动神经元逐渐丧失,这是测试FBMs可能作用的理想遗传模型。我们证明,新生小鼠出生后运动功能受损,导致致命的呼吸衰竭。接下来,我们表明,妊娠晚期胚胎的肺泡间隔增厚,肺泡面积减小,而肺发育分子标志物的表达不受影响。重要的是,妊娠晚期胚胎的肺淋巴管扩张,产前肺淋巴功能降低。我们的结果表明,小鼠表现出包括FBMs在内的运动功能受损,妊娠晚期胚胎的产前淋巴功能降低,肺扩张受损,表现为肺泡间隔增厚和肺泡面积减小,这是为发育中的肺在出生时充气做准备。这些发现提示了一种可能的机制,即FBMs与出生后的呼吸运动类似,刺激缺乏平滑肌覆盖的肺收集淋巴管中的产前淋巴功能,为发育中的肺在出生时充气和气体交换做好准备。此外,这些结果增加了在妊娠晚期刺激FBMs可能是降低新生儿呼吸衰竭发生风险的有效方法的可能性。