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  Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation

Li, S., Harrison, D., Carbonetto, S., Fässler, R., Smyth, N., Edgar, D., et al. (2002). Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation. Journal of Cell Biology, 157(7), 1279-1290.

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Genre: Journal Article
Alternative Title : J. Cell Biol.

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 Creators:
Li, S., Author
Harrison, D., Author
Carbonetto, S., Author
Fässler, R.1, Author           
Smyth, N., Author
Edgar, D., Author
Yurchenco, P. D., Author
Affiliations:
1Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565147              

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Free keywords: basement membrane; gastrulation; integrin; dystroglycan; apoptosis
 Abstract: Laminin-1 is essential for early embryonic basement membrane assembly and differentiation. Several steps can be distinguished, i.e., the expression of laminin and companion matrix components, their accumulation on the cell surface and assembly into basement membrane between endoderm and inner cell mass, and the ensuing differentiation of epiblast. In this study, we used differentiating embryoid bodies derived from mouse embryonic stem cells null for gamma1-laminin, beta1- integrin and alpha/beta-dystroglycan to dissect the contributions of laminin domains and interacting receptors to this process. We found that (a) laminin enables beta1-integrin- null embryoid bodies to assemble basement membrane and achieve epiblast with beta1-integrin enabling expression of the laminin alpha1 subunit; (b) basement membrane assembly and differentiation require laminin polymerization in conjunction with cell anchorage, the latter critically dependent upon a heparin-binding locus within LG module-4; (c) dystroglycan is not uniquely required for basement membrane assembly or initial differentiation; (d) dystroglycan and integrin cooperate to sustain survival of the epiblast and regulate laminin expression; and (e) laminin, acting via beta1-integrin through LG1-3 and requiring polymerization, can regulate dystroglycan expression.

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Language(s): eng - English
 Dates: 2002-06-24
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 31387
ISI: 000176528400016
 Degree: -

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Title: Journal of Cell Biology
  Alternative Title : J. Cell Biol.
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 157 (7) Sequence Number: - Start / End Page: 1279 - 1290 Identifier: ISSN: 0021-9525