Saadoon Ammar, Ambalavanan Namasivayam, Zinn Kurt, Ashraf Ambika P, MacEwen Mark, Nicola Teodora, Fanucchi Michelle V, Harris William T
1 Departments of Pediatrics.
2 Radiology, and.
Am J Respir Cell Mol Biol. 2017 Mar;56(3):383-392. doi: 10.1165/rcmb.2014-0482OC.
Epidemiologic studies have linked gestational vitamin D deficiency to respiratory diseases, although mechanisms have not been defined. We hypothesized that antenatal vitamin D deficiency would impair airway development and alveolarization in a mouse model. We studied the effect of antenatal vitamin D deficiency by inducing it in pregnant mice and then compared lung development and function in their offspring to littermate controls. Postnatal vitamin D deficiency and sufficiency models from each group were also studied. We developed a novel tracheal ultrasound imaging technique to measure tracheal diameter in vivo. Histological analysis estimated tracheal cartilage total area and thickness. We found that vitamin D-deficient pups had reduced tracheal diameter with decreased tracheal cartilage minimal width. Vitamin D deficiency increased airway resistance and reduced lung compliance, and led to alveolar simplification. Postnatal vitamin D supplementation improved lung function and radial alveolar count, a parameter of alveolar development, but did not correct tracheal narrowing. We conclude that antenatal vitamin D deficiency impairs airway and alveolar development and limits lung function. Reduced tracheal diameter, cartilage irregularity, and alveolar simplification in vitamin D-deficient mice may contribute to increased airways resistance and diminished lung compliance. Vitamin D supplementation after birth improved lung function and, potentially, alveolar simplification, but did not improve defective tracheal structure. This mouse model offers insight into the mechanisms of vitamin D deficiency-associated lung disease and provides an in vivo model for investigating preclinical preventive and therapeutic strategies.
流行病学研究已将孕期维生素D缺乏与呼吸系统疾病联系起来,尽管其机制尚未明确。我们推测,在小鼠模型中,产前维生素D缺乏会损害气道发育和肺泡化。我们通过在怀孕小鼠中诱导产前维生素D缺乏来研究其影响,然后将其后代的肺发育和功能与同窝对照进行比较。还研究了每组的产后维生素D缺乏和充足模型。我们开发了一种新型气管超声成像技术来在体内测量气管直径。组织学分析估计气管软骨的总面积和厚度。我们发现,维生素D缺乏的幼崽气管直径减小,气管软骨最小宽度降低。维生素D缺乏会增加气道阻力并降低肺顺应性,并导致肺泡简化。产后补充维生素D可改善肺功能和肺泡发育参数——径向肺泡计数,但并未纠正气管狭窄。我们得出结论,产前维生素D缺乏会损害气道和肺泡发育并限制肺功能。维生素D缺乏小鼠的气管直径减小、软骨不规则和肺泡简化可能导致气道阻力增加和肺顺应性降低。出生后补充维生素D可改善肺功能,并可能改善肺泡简化,但并未改善有缺陷的气管结构。该小鼠模型有助于深入了解维生素D缺乏相关肺部疾病的机制,并为研究临床前预防和治疗策略提供体内模型。