Atkinson Jeffrey J, Holmbeck Kenn, Yamada Susan, Birkedal-Hansen Henning, Parks William C, Senior Robert M
Department of Internal Medicine, Pulmonary and Critical Care Division, Washington University School of Medicine, St. Louis, Missouri, USA.
Dev Dyn. 2005 Apr;232(4):1079-90. doi: 10.1002/dvdy.20267.
Matrix metalloproteinases (MMPs) are expressed during lung development, but their role may be limited, as mice deficient in MMP-3, 7, 9, or 12 develop a normal adult lung. Because membrane-type 1 matrix metalloproteinase (MT1-MMP) is expressed in the developing lung epithelium, we examined the lung structure of MT1-MMP-deficient (-/-) mice. Branching morphogenesis was normal, but alveolar development was abnormal in the MT1-MMP-/- lungs with 40% less alveolar surface area at 1 month (P < 0.01). MT1-MMP-/- airways and alveoli had an abnormal ultrastructural appearance, but epithelial cell differentiation markers were distributed similarly in both strains. There was no evidence of excess extracellular matrix deposition or inflammation at the time points examined. In contrast, by adulthood MMP-2-/- mice had normal alveolar size and structure, indicating normal alveolar development was not dependent on the ability of MT1-MMP to activate pro-MMP-2. These data indicate that MT1-MMP is required for normal lung development.
基质金属蛋白酶(MMPs)在肺发育过程中表达,但其作用可能有限,因为缺乏MMP - 3、7、9或12的小鼠可发育出正常的成年肺。由于膜型1基质金属蛋白酶(MT1 - MMP)在发育中的肺上皮细胞中表达,我们研究了MT1 - MMP基因敲除(- / -)小鼠的肺结构。分支形态发生正常,但MT1 - MMP - / - 小鼠的肺泡发育异常,在1个月时肺泡表面积减少40%(P < 0.01)。MT1 - MMP - / - 的气道和肺泡具有异常的超微结构外观,但上皮细胞分化标志物在两种品系中的分布相似。在所检查的时间点没有细胞外基质过度沉积或炎症的证据。相比之下,成年期的MMP - 2 - / - 小鼠具有正常的肺泡大小和结构,表明正常的肺泡发育不依赖于MT1 - MMP激活前MMP - 2的能力。这些数据表明MT1 - MMP是正常肺发育所必需的。