Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation
Author:
Miner Jeffrey H.12, Li Cong1, Mudd Jacqueline L.1, Go Gloriosa1, Sutherland Ann E.3
Affiliation:
1. Renal Division, Washington University School of Medicine, St Louis, MO 63110,USA 2. Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, MO 63110, USA 3. Department of Cell Biology, University of Virginia, Charlottesville, VA 22908,USA
Abstract
Laminins are components of all basement membranes and have well demonstrated roles in diverse developmental processes, from the peri-implantation period onwards. Laminin 1 (α1β1γ1) is a major laminin found at early stages of embryogenesis in both embryonic and extraembryonic basement membranes. The laminin γ1 chain has been shown by targeted mutation to be required for endodermal differentiation and formation of basement membranes; Lamc1-/- embryos die within a day of implantation. We report the generation of mice lacking lamininα1 and laminin β1, the remaining two laminin 1 chains. Mutagenic insertions in both Lama1 and Lamb1 were obtained in a secretory gene trap screen. Lamb1-/- embryos are similar to Lamc1-/- embryos in that they lack basement membranes and do not survive beyond embryonic day (E) 5.5. However, in Lama1-/- embryos, the embryonic basement membrane forms,the embryonic ectoderm cavitates and the parietal endoderm differentiates,apparently because laminin 10 (α5β1γ1) partially compensates for the absent laminin 1. However, such compensation did not occur for Reichert's membrane, which was absent, and the embryos died by E7. Overexpression of laminin α5 from a transgene improved the phenotype of Lama1-/- embryos to the point that they initiated gastrulation, but this overexpression did not rescue Reichert's membrane, and trophoblast cells did not form blood sinuses. These data suggest that both the molecular composition and the integrity of basement membranes are crucial for early developmental events.
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Reference53 articles.
1. Abrahamson, D. R., Irwin, M. H., St. John, P. L., Perry, E. W.,Accavitti, M. A., Heck, L. W. and Couchman, J. R. (1989). Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: localization of the end of the long arm and the short arms to discrete microdomains. J. Cell Biol.109,3477-3491. 2. Bolcato-Bellemin, A. L., Lefebvre, O., Arnold, C., Sorokin, L.,Miner, J. H., Kedinger, M. and Simon-Assmann, P. (2003). Laminin alpha5 chain is required for intestinal smooth muscle development. Dev. Biol.260,376-390. 3. Burgeson, R. E., Chiquet, M., Deutzmann, R., Ekblom, P., Engel,J., Kleinman, H., Martin, G. R., Ortonne, J.-P., Paulsson, M., Sanes, J. et al. (1994). A new nomenclature for laminins. Matrix Biol.14,209-211. 4. Cheng, Y.-S., Champliaud, M.-F., Burgeson, R. E., Marinkovich,M. P. and Yurchenco, P. D. (1997). Self-assembly of laminin isoforms. J. Biol. Chem.272,31525-31532. 5. Colognato, H., Winkelmann, D. A. and Yurchenco, P. D.(1999). Laminin polymerization induces a receptor-cytoskeleton network. J. Cell Biol.145,619-631.
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