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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[1]   DEVELOPMENTAL EXPRESSION OF NICEIN ADHESION PROTEIN (LAMININ-5) SUBUNITS SUGGESTS MULTIPLE MORPHOGENIC ROLES [J].
ABERDAM, D ;
AGUZZI, A ;
BAUDOIN, C ;
GALLIANO, MF ;
ORTONNE, JP ;
MENEGUZZI, G .
CELL ADHESION AND COMMUNICATION, 1994, 2 (02) :115-129
[2]   Uncoordinated production of Laminin-5 chains in airways epithelium of allergic asthmatics -: art. no. 110 [J].
Amin, K ;
Janson, C ;
Sevéus, L ;
Miyazaki, K ;
Virtanen, I ;
Venge, P .
RESPIRATORY RESEARCH, 2005, 6 (1)
[3]   Membrane-type 1 matrix metalloproteinase is required for normal alveolar development [J].
Atkinson, JJ ;
Holmbeck, K ;
Yamada, S ;
Birkedal-Hansen, H ;
Parks, WC ;
Senior, RM .
DEVELOPMENTAL DYNAMICS, 2005, 232 (04) :1079-1090
[4]   A simplified laminin nomenclature [J].
Aumailley, M ;
Bruckner-Tuderman, L ;
Carter, WG ;
Deutzmann, R ;
Edgar, D ;
Ekblom, P ;
Engel, J ;
Engvall, E ;
Hohenester, E ;
Jones, JCR ;
Kleinman, HK ;
Marinkovich, MP ;
Martin, GR ;
Mayer, U ;
Meneguzzi, G ;
Miner, JH ;
Miyazaki, K ;
Patarroyo, M ;
Paulsson, M ;
Quaranta, V ;
Sanes, JR ;
Sasaki, T ;
Sekiguchi, K ;
Sorokin, LM ;
Talts, JF ;
Tryggvason, K ;
Uitto, J ;
Virtanen, I ;
von der Mark, K ;
Wewer, UM ;
Yamada, Y ;
Yurchenco, PD .
MATRIX BIOLOGY, 2005, 24 (05) :326-332
[5]   Laminin α5 chain is required for intestinal smooth muscle development [J].
Bolcato-Bellemin, AL ;
Lefebvre, O ;
Arnold, C ;
Sorokin, L ;
Miner, JH ;
Kedinger, M ;
Simon-Assmann, P .
DEVELOPMENTAL BIOLOGY, 2003, 260 (02) :376-390
[6]   EPILIGRIN, A NEW CELL-ADHESION LIGAND FOR INTEGRIN ALPHA-3-BETA-1 IN EPITHELIAL BASEMENT-MEMBRANES [J].
CARTER, WG ;
RYAN, MC ;
GAHR, PJ .
CELL, 1991, 65 (04) :599-610
[7]   Distribution of laminin 5, integrin receptors, and branching morphogenesis during human fetal lung development [J].
Coraux, C ;
Meneguzzi, G ;
Rousselle, P ;
Puchelle, E ;
Gaillard, D .
DEVELOPMENTAL DYNAMICS, 2002, 225 (02) :176-185
[8]   Complete sequence, recombinant analysis and binding to laminins and sulphated ligands of the N-terminal domains of laminin α3B and α5 chains [J].
Garbe, JHO ;
Göhring, W ;
Mann, K ;
Timpl, R ;
Sasaki, T .
BIOCHEMICAL JOURNAL, 2002, 362 :213-221
[9]   Laminin γ3 chain binds to nidogen and is located in murine basement membranes [J].
Gersdorff, N ;
Kohfeldt, E ;
Sasaki, T ;
Timpl, R ;
Miosge, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (23) :22146-22153
[10]   Modulation of pulmonary alveolar type II cell phenotype and communication by extracellular matrix and KGF [J].
Isakson, BE ;
Lubman, RL ;
Seedorf, GJ ;
Boitano, S .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 281 (04) :C1291-C1299