Massaro D, Massaro G D
Lung Biology Laboratory, Georgetown University School of Medicine, Washington, DC 20007-2197, USA.
Novartis Found Symp. 2001;234:229-36; discussion 236-41. doi: 10.1002/0470868678.ch14.
Pulmonary alveoli, the lung's gas-exchange structures, are formed in part by subdivision (septation) of the saccules that constitute the gas-exchange region of the immature lung. Although little is known about the regulation of septation, relatively recent studies show: (1) all-trans retinoic acid (RA) treatment of newborn rats increases septation and prevents the inhibition of septation produced by treatment of newborn rats with dexamethasone, a glucocorticosteroid hormone; (2) treatment with RA of adult rats that have elastase-induced emphysema increases lung elastic recoil, induces the formation of alveoli, and increases volume-corrected alveolar surface area; and (3) in tight-skin mice, which have a genetic failure of septation, and in rats in which septation had previously been prevented by treatment with dexamethasone, treatment with RA partially rescues the failed septation. These findings raise the possibility that treatment with RA will induce the formation of alveoli in humans with pulmonary emphysema.
肺泡是肺的气体交换结构,部分由构成未成熟肺气体交换区域的囊泡细分(间隔形成)而成。尽管对于间隔形成的调节知之甚少,但最近的研究表明:(1)用全反式视黄酸(RA)处理新生大鼠可增加间隔形成,并防止地塞米松(一种糖皮质激素)处理新生大鼠所产生的间隔形成抑制;(2)用RA处理患有弹性蛋白酶诱导性肺气肿的成年大鼠可增加肺弹性回缩力,诱导肺泡形成,并增加经体积校正的肺泡表面积;(3)在间隔形成存在遗传缺陷的紧皮小鼠以及先前用地塞米松处理已阻止间隔形成的大鼠中,用RA处理可部分挽救失败的间隔形成。这些发现增加了用RA治疗将在人类肺气肿患者中诱导肺泡形成的可能性。