Literature DB >> 8983017

Molecular complexity of the cutaneous basement membrane zone.

J Uitto1, L Pulkkinen.   

Abstract

Ultrastructural examination of the cutaneous basement membrane zone (BMZ) reveals the presence of several attachment structures, which are critical for integrity of the stable association of epidermis and dermis. These include hemidesmosomes which extend from the intracellular compartment of the basal keratinocyte to the underlying basement membrane where they complex with anchoring filaments, thread-like structures traversing the lamina lucida. At the lower portion of dermal-epidermal attachment zone, anchoring fibrils extend from the lamina densa to the papillary dermis, where they associate with basement membrane-like structures, known as anchoring plaques. Molecular cloning of the cutaneous BMZ components has allowed elucidation of the structural features of the proteins which constitute these attachment structures. Specifically, hemidesmosomes have been shown to consist of at least four distinct proteins. The intracellular hemidesmosomal inner plaque is comprised of the 230-kD bullous pemphigoid antigen (BPAG1), and plectin, a high-molecular weight cytomatrix protein, encoded by the corresponding gene, PLEC1. The transmembrane component of the hemidesmosomes consists of the 180-kD bullous pemphigoid antigen (BPAG2), a collagenous protein also known as type XVII collagen (COL17A1), as well as of the basal keratinocyte-specific integrin alpha 6 beta 4. The anchoring filaments consist predominantly of laminin 5 with three constitutive subunit polypeptides, the alpha 3, beta 3 and gamma 2 chains, which is associated with laminin 6 with the chain composition alpha 3, beta 1 and gamma 1. Also associated with anchoring filaments is a novel protein, ladinin, which serves as autoantigen in the linear IgA disease, and the corresponding gene, LAD1, has been mapped to human chromosome 1. Finally, the major, if not the exclusive, component of anchoring fibrils is type VII collagen, encoded by the gene (COL7A1) which consists of 118 distinct exons, the largest number of exons in any gene published thus far. Collectively, the cutaneous basement membrane zone is a complex continuum of macromolecules which form a network providing the stable association of the epidermis to the underlying dermis. Thus, genetic lesions resulting in abnormalities in any part of this network could result in a blistering skin disease, such as epidermolysis bullosa.

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Year:  1996        PMID: 8983017     DOI: 10.1007/bf00357071

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  52 in total

Review 1.  Intermediate filaments in disease.

Authors:  W H McLean; E B Lane
Journal:  Curr Opin Cell Biol       Date:  1995-02       Impact factor: 8.382

Review 2.  Desmosomes and hemidesmosomes.

Authors:  D R Garrod
Journal:  Curr Opin Cell Biol       Date:  1993-02       Impact factor: 8.382

3.  A new nomenclature for the laminins.

Authors:  R E Burgeson; M Chiquet; R Deutzmann; P Ekblom; J Engel; H Kleinman; G R Martin; G Meneguzzi; M Paulsson; J Sanes
Journal:  Matrix Biol       Date:  1994-04       Impact factor: 11.583

4.  Molecular biology of the 230-kD bullous pemphigoid antigen. Cloning of the BPAG1 gene and its tissue-specific expression.

Authors:  K Tamai; D Sawamura; H Y Choi Do; K Li; J Uitto
Journal:  Dermatology       Date:  1994       Impact factor: 5.366

5.  Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.

Authors:  J A McGrath; B Gatalica; K Li; M G Dunnill; J R McMillan; A M Christiano; R A Eady; J Uitto
Journal:  Am J Pathol       Date:  1996-06       Impact factor: 4.307

6.  Human autoantibodies against the 230-kD bullous pemphigoid antigen (BPAG1) bind only to the intracellular domain of the hemidesmosome, whereas those against the 180-kD bullous pemphigoid antigen (BPAG2) bind along the plasma membrane of the hemidesmosome in normal human and swine skin.

Authors:  A Ishiko; H Shimizu; A Kikuchi; T Ebihara; T Hashimoto; T Nishikawa
Journal:  J Clin Invest       Date:  1993-04       Impact factor: 14.808

7.  Human type VII collagen: cDNA cloning and chromosomal mapping of the gene.

Authors:  M G Parente; L C Chung; J Ryynänen; D T Woodley; K C Wynn; E A Bauer; M G Mattei; M L Chu; J Uitto
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-15       Impact factor: 11.205

8.  Genomic organization of collagenous domains and chromosomal assignment of human 180-kDa bullous pemphigoid antigen-2, a novel collagen of stratified squamous epithelium.

Authors:  K H Li; D Sawamura; G J Giudice; L A Diaz; M G Mattei; M L Chu; J Uitto
Journal:  J Biol Chem       Date:  1991-12-15       Impact factor: 5.157

9.  Identification of a new hemidesmosomal protein, HD1: a major, high molecular mass component of isolated hemidesmosomes.

Authors:  Y Hieda; Y Nishizawa; J Uematsu; K Owaribe
Journal:  J Cell Biol       Date:  1992-03       Impact factor: 10.539

10.  Human amnion contains a novel laminin variant, laminin 7, which like laminin 6, covalently associates with laminin 5 to promote stable epithelial-stromal attachment.

Authors:  M F Champliaud; G P Lunstrum; P Rousselle; T Nishiyama; D R Keene; R E Burgeson
Journal:  J Cell Biol       Date:  1996-03       Impact factor: 10.539

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  21 in total

1.  Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa.

Authors:  L Pulkkinen; F Bullrich; P Czarnecki; L Weiss; J Uitto
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

Review 2.  Extracellular matrix molecules: potential targets in pharmacotherapy.

Authors:  Hannu Järveläinen; Annele Sainio; Markku Koulu; Thomas N Wight; Risto Penttinen
Journal:  Pharmacol Rev       Date:  2009-06       Impact factor: 25.468

Review 3.  Cellular and molecular partners involved in gut morphogenesis and differentiation.

Authors:  M Kedinger; O Lefebvre; I Duluc; J N Freund; P Simon-Assmann
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1998-06-29       Impact factor: 6.237

4.  Epidermolysis bullosa with pyloric atresia: novel mutations in the beta4 integrin gene (ITGB4).

Authors:  L Pulkkinen; D U Kim; J Uitto
Journal:  Am J Pathol       Date:  1998-01       Impact factor: 4.307

Review 5.  Epithelial growth and differentiation: an overview.

Authors:  T T Sun
Journal:  Mol Biol Rep       Date:  1996       Impact factor: 2.316

6.  Cloning of the human type XVII collagen gene (COL17A1), and detection of novel mutations in generalized atrophic benign epidermolysis bullosa.

Authors:  B Gatalica; L Pulkkinen; K Li; K Kuokkanen; M Ryynänen; J A McGrath; J Uitto
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

Review 7.  Gene therapy for skin diseases.

Authors:  Emily Gorell; Ngon Nguyen; Alfred Lane; Zurab Siprashvili
Journal:  Cold Spring Harb Perspect Med       Date:  2014-04-01       Impact factor: 6.915

8.  Expression of Laminin γ2 Proteolytic Fragments in Murine Skin Following Exposure to Sulfur Mustard.

Authors:  Yoke-Chen Chang; James D Wang; Hui-Ying Chang; Peihong Zhou; Rita A Hahn; Marion K Gordon; Jeffrey D Laskin; Donald R Gerecke
Journal:  Anat Rec (Hoboken)       Date:  2020-05-18       Impact factor: 2.064

9.  Plectin regulates the organization of glial fibrillary acidic protein in Alexander disease.

Authors:  Rujin Tian; Martin Gregor; Gerhard Wiche; James E Goldman
Journal:  Am J Pathol       Date:  2006-03       Impact factor: 4.307

Review 10.  Collagens.

Authors:  Marion K Gordon; Rita A Hahn
Journal:  Cell Tissue Res       Date:  2009-08-20       Impact factor: 5.249

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