Bultmann-Mellin Insa, Dinger Katharina, Debuschewitz Carolin, Loewe Katharina M A, Melcher Yvonne, Plum Miro T W, Appel Sarah, Rappl Gunter, Willenborg Sebastian, Schauss Astrid C, Jüngst Christian, Krüger Marcus, Dressler Sven, Nakamura Tomoyuki, Wempe Frank, Alejandre Alcázar Miguel A, Sterner-Kock Anja
Center for Experimental Medicine, Medical Faculty, University of Cologne, Cologne, Germany.
Department of Pediatrics and Adolescent Medicine, Medical Faculty, University of Cologne, Cologne, Germany.
Am J Physiol Lung Cell Mol Physiol. 2017 Oct 1;313(4):L687-L698. doi: 10.1152/ajplung.00031.2017. Epub 2017 Jul 6.
Deficiency of the extracellular matrix protein latent transforming growth factor-β (TGF-β)-binding protein-4 (LTBP4) results in lack of intact elastic fibers, which leads to disturbed pulmonary development and lack of normal alveolarization in humans and mice. Formation of alveoli and alveolar septation in pulmonary development requires the concerted interaction of extracellular matrix proteins, growth factors such as TGF-β, fibroblasts, and myofibroblasts to promote elastogenesis as well as vascular formation in the alveolar septae. To investigate the role of LTBP4 in this context, lungs of LTBP4-deficient () mice were analyzed in close detail. We elucidate the role of LTBP4 in pulmonary alveolarization and show that three different, interacting mechanisms might contribute to alveolar septation defects in lungs: ) absence of an intact elastic fiber network, ) reduced angiogenesis, and ) upregulation of TGF-β activity resulting in profibrotic processes in the lung.
细胞外基质蛋白潜伏转化生长因子-β(TGF-β)结合蛋白-4(LTBP4)的缺乏会导致弹性纤维不完整,进而导致人类和小鼠的肺发育紊乱以及正常肺泡化缺失。肺发育过程中肺泡的形成和肺泡间隔的形成需要细胞外基质蛋白、TGF-β等生长因子、成纤维细胞和肌成纤维细胞协同相互作用,以促进弹性纤维生成以及肺泡间隔中的血管形成。为了研究LTBP4在此过程中的作用,我们对LTBP4基因敲除()小鼠的肺进行了详细分析。我们阐明了LTBP4在肺泡化中的作用,并表明三种不同的相互作用机制可能导致肺中肺泡间隔缺陷:)缺乏完整的弹性纤维网络,)血管生成减少,以及)TGF-β活性上调导致肺中的纤维化过程。