Lung development in laminin γ2 deficiency:: abnormal tracheal hemidesmosomes with normal branching morphogenesis and epithelial differentiation

被引:21
作者
Nguyen, NM
Pulkkinen, L
Schlueter, JA
Meneguzzi, G
Uitto, J
Senior, RM [1 ]
机构
[1] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
[3] Univ Kuopio, Dept Clin Nutr, FIN-70211 Kuopio, Finland
[4] Univ Nice, Sch Med, Nice, France
[5] Thomas Jefferson Univ, Jefferson Med Coll, Dept Dermatol & Cutaneous Biol, Philadelphia, PA 19107 USA
[6] Thomas Jefferson Univ, Jefferson Med Coll, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
关键词
D O I
10.1186/1465-9921-7-28
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Laminin gamma 2 (Lamc2), one of the polypeptides in laminin-332 (laminin-5), is prominent in the basement membrane of alveolar walls and airways of developing and adult lung. Laminins are important for lung morphogenesis and based on its localization, a function for laminin gamma 2 in lung development has been hypothesized. Targeted deletion of the laminin gamma 2 gene in mice results in skin blistering and neonatal death at 3-5 days after birth due to failure to thrive. Methods: Examination of lung development in Lamc2-/- mice through 1-2 days postnatal was accomplished by morphometric analysis, lung bud culture, electron microscopy, immunohistochemical and immunofluorescence staining. Results: Compared to littermate controls, Lamc2-/- lungs were similar in morphology during embryonic life. At post-natal day 1-2, distal saccules were mildly dilated by chord length measurements. Epithelial differentiation as evaluated by immunohistochemical staining for markers of ciliated cells, Clara cells, alveolar type I cells and alveolar type II cells did not reveal a difference between Lamc2-/- and littermate control lungs. Likewise, vascular development, smooth muscle cell differentiation, and elastic fiber formation looked similar, as did airway basement membrane ultrastructure. Branching morphogenesis by lung bud culture was similar in Lamc2-/- and littermate control lungs. Since laminin-332 is important for hemidesmosome formation, we examined the structure of tracheal hemidesmosomes by transmission electron microscopy. Compared to littermate controls, Lamc2-/- tracheal hemidesmosomes were less organized and lacked the increased electron density associated with the basement membrane abutting the hemidesmosome. Conclusion: These findings indicate that laminin gamma 2 and laminin-332, despite their prominence in the lung, have a minimal role in lung development through the saccular stage.
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页数:12
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