Structure and function of hemidesmosomes: more than simple adhesion complexes
- PMID: 10201522
- DOI: 10.1046/j.1523-1747.1999.00546.x
Structure and function of hemidesmosomes: more than simple adhesion complexes
Abstract
The attachment of cells to the extracellular matrix is of crucial importance in the maintenance of tissue structure and integrity. In stratified epithelia such as in skin as well as in other complex epithelia multiprotein complexes called hemidesmosomes are involved in promoting the adhesion of epithelial cells to the underlying basement membrane. In the past few years our understanding of the role of hemidesmosomes has improved considerably. Their importance has become apparent in clinical conditions, in which absence or defects of hemidesmosomal proteins result in devastating blistering diseases of the skin. Molecular genetic studies have increased our knowledge of the function of the various components of hemidesmosomes and enabled the characterization of protein-protein interactions involved in their assembly. It has become clear that the alpha6beta4 integrin, a major component of hemidesmosomes, is able to transduce signals from the extracellular matrix to the interior of the cell, that critically modulate the organization of the cytoskeleton, proliferation, apoptosis, and differentiation. Nevertheless, our knowledge of the mechanisms regulating the functional state of hemidesmosomes and, hence, the dynamics of cell adhesion, a process of crucial importance in development, wound healing or tumor invasion, remains limited. The aims of this review are to highlight the recent progresses of our knowledge on the organization and assembly of hemidesmosomes, their involvement in signaling pathways as well as their participation in clinical pathologic conditions.
Similar articles
-
The dento-epithelial junction: cell adhesion by type I hemidesmosomes in the absence of a true basal lamina.J Periodontol. 2001 Jun;72(6):788-97. doi: 10.1902/jop.2001.72.6.788. J Periodontol. 2001. PMID: 11453242
-
Hemidesmosomes and their unique transmembrane protein BP180.Microsc Res Tech. 1998 Nov 1;43(3):207-17. doi: 10.1002/(SICI)1097-0029(19981101)43:3<207::AID-JEMT2>3.0.CO;2-Z. Microsc Res Tech. 1998. PMID: 9840798 Review.
-
[Molecular architecture of hemidesmosomes and desmosomes].Seikagaku. 1999 Dec;71(12):1417-31. Seikagaku. 1999. PMID: 10659676 Review. Japanese. No abstract available.
-
Analysis of the interactions between BP180, BP230, plectin and the integrin alpha6beta4 important for hemidesmosome assembly.J Cell Sci. 2003 Jan 15;116(Pt 2):387-99. doi: 10.1242/jcs.00241. J Cell Sci. 2003. PMID: 12482924
-
A recombinant tail-less integrin beta 4 subunit disrupts hemidesmosomes, but does not suppress alpha 6 beta 4-mediated cell adhesion to laminins.J Cell Biol. 1995 Apr;129(2):473-87. doi: 10.1083/jcb.129.2.473. J Cell Biol. 1995. PMID: 7721947 Free PMC article.
Cited by
-
Adenovirus-Mediated LAMA3 Transduction Enhances Hemidesmosome Formation and Periodontal Reattachment during Wound Healing.Mol Ther Methods Clin Dev. 2020 Jun 4;18:291-303. doi: 10.1016/j.omtm.2020.06.001. eCollection 2020 Sep 11. Mol Ther Methods Clin Dev. 2020. PMID: 32671133 Free PMC article.
-
Cell Junctions in Periodontal Health and Disease: An Insight.Eur J Dent. 2024 May;18(2):448-457. doi: 10.1055/s-0043-1775726. Epub 2023 Dec 4. Eur J Dent. 2024. PMID: 38049123 Free PMC article.
-
The matrix protein CCN1/CYR61 is required for α(V)β5-mediated cancer cell migration.Cell Biochem Funct. 2012 Dec;30(8):687-95. doi: 10.1002/cbf.2853. Epub 2012 Jun 13. Cell Biochem Funct. 2012. PMID: 22692860 Free PMC article.
-
SHP2 mediates the localized activation of Fyn downstream of the α6β4 integrin to promote carcinoma invasion.Mol Cell Biol. 2010 Nov;30(22):5306-17. doi: 10.1128/MCB.00326-10. Epub 2010 Sep 20. Mol Cell Biol. 2010. PMID: 20855525 Free PMC article.
-
The pathophysiology of bullous pemphigoid.Clin Rev Allergy Immunol. 2007 Oct;33(1-2):67-77. doi: 10.1007/s12016-007-0030-y. Clin Rev Allergy Immunol. 2007. PMID: 18094948 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous