Pattern formation in type-I superconducting films

2007 ◽  
Vol 101 (9) ◽  
pp. 09G118 ◽  
Author(s):  
V. Jeudy ◽  
C. Gourdon ◽  
A. Cēbers ◽  
T. Okada
1990 ◽  
Vol 165-166 ◽  
pp. 1471-1472 ◽  
Author(s):  
A. Favre ◽  
E. Holguin ◽  
B. Dutoit ◽  
L. Rinderer

2007 ◽  
Vol 460-462 ◽  
pp. 1228-1229 ◽  
Author(s):  
G.R. Berdiyorov ◽  
M.V. Milošević ◽  
F.M. Peeters

Development ◽  
1990 ◽  
Vol 110 (4) ◽  
pp. 1091-1099 ◽  
Author(s):  
L. Schuger ◽  
K.S. O'Shea ◽  
B.B. Nelson ◽  
J. Varani

The behavior of embryonic murine lung cells on a basement membrane extract (Matrigel) was investigated. Single cell suspensions generated by trypsinization of lungs removed from day 12 embryos were plated on Matrigel and cultured for up to one week. The basement membrane extract was used as a gel, and as a wet or dried film. In all of these instances, organotypic arrangement of the embryonic lung cells was observed. This process consisted of cell aggregation, sorting, polarization and formation of a tridimensional organization resembling embryonic lung. The maximal degree of organotypic development was obtained by using a thick gel; minimal reorganization was observed using a dried film. A rabbit polyclonal serum to laminin inhibited organotypic pattern formation while normal rabbit serum did not. Culture of lung cells on laminin gels promoted epithelial cyst formation but poor mesenchymal organization. By studying the behavior of epithelial and/or mesenchymal enriched cell populations on Matrigel, it was concluded that organotypic pattern formation on Matrigel required the presence of both cell populations. Cultivation of dissociated lung cells on a gel consisting of a mixture of collagens type I and III (Vitrogen-100) produced only cell aggregation. Cultivation of lung cells on a thin film of Vitrogen-100 or on uncoated tissue culture plastic produced monolayers of mesenchymal cells alone. Cultivation of lung cells in suspension also failed to induce organotypic arrangement even at maximal cell densities. The present study strongly supports a role for the basement membrane in the organotypic rearrangement of embryonic lung cells and subsequent in vitro cyst formation and budding of the reestablished epithelium. This, in turn, reinforces the concept of the basement membrane as a major regulator of organogenesis.


1969 ◽  
Vol 185 (2) ◽  
pp. 653-663 ◽  
Author(s):  
Paul Tholfsen ◽  
Hans Meissner

2004 ◽  
Vol 322 (1-2) ◽  
pp. 111-116 ◽  
Author(s):  
L.M. Abreu ◽  
A.P.C. Malbouisson

Development ◽  
2001 ◽  
Vol 128 (6) ◽  
pp. 859-869 ◽  
Author(s):  
K.A. Mintzer ◽  
M.A. Lee ◽  
G. Runke ◽  
J. Trout ◽  
M. Whitman ◽  
...  

TGFbeta signaling pathways of the bone morphogenetic protein (BMP) subclass are essential for dorsoventral pattern formation of both vertebrate and invertebrate embryos. Here we determine by chromosomal mapping, linkage analysis, cDNA sequencing and mRNA rescue that the dorsalized zebrafish mutant lost-a-fin (laf) is defective in the gene activin receptor-like kinase 8 (alk8), which encodes a novel type I TGFbeta receptor. The alk8 mRNA is expressed both maternally and zygotically. Embyros that lack zygotic, but retain maternal Laf/Alk8 activity, display a weak dorsalization restricted to the tail and die by 3 days postfertilization. We rescued the laf dorsalized mutant phenotype by alk8 mRNA injection and generated homozygous laf/alk8 mothers to investigate the maternal role of Laf/Alk8 activity. Adult fish lacking Laf/Alk8 activity are fertile, exhibit a growth defect and are significantly smaller than their siblings. Embryos derived from homozygous females, which lack both maternal and zygotic Laf/Alk8 activity, display a strongly dorsalized mutant phenotype, no longer limited to the tail. These mutant embryos lack almost all gastrula ventral cell fates, with a concomitant expansion of dorsal cell types. During later stages, most of the somitic mesoderm and neural tissue circumscribe the dorsoventral axis of the embryo. Zygotic laf/alk8 mutants can be rescued by overexpression of the BMP signal transducer Smad5, but not the Bmp2b or Bmp7 ligands, consistent with the Laf/Alk8 receptor acting within a BMP signaling pathway, downstream of a Bmp2b/Bmp7 signal. Antibodies specific for the phosphorylated, activated form of Smad1/5, show that BMP signaling is nearly absent in gastrula lacking both maternal and zygotic Laf/Alk8 activity, providing further evidence that Laf/Alk8 transduces a BMP signal. In total, our work strongly supports the role of Laf/Alk8 as a type I BMP receptor required for the specification of ventral cell fates.


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