Type VII collagen gene expression by cultured human cells and in fetal skin. Abundant mRNA and protein levels in epidermal keratinocytes
- PMID: 1729268
- PMCID: PMC442832
- DOI: 10.1172/JCI115557
Type VII collagen gene expression by cultured human cells and in fetal skin. Abundant mRNA and protein levels in epidermal keratinocytes
Abstract
Type VII collagen, a genetically distinct member of the collagen family, is present in the cutaneous basement membrane zone as an integral component of the anchoring fibrils. We have recently isolated several cDNAs that correspond to human type VII collagen sequences. One of these cDNAs (clone K-131) was utilized to examine type VII collagen gene expression in cultures of human cells by Northern analyses, in situ hybridizations and indirect immunofluorescence. Northern hybridizations revealed the presence of an approximately 9-kb mRNA transcript, and indicated a high level of expression in epidermal keratinocytes as well as in an oral epidermoid carcinoma cell line (KB), while the expression was considerably lower in skin fibroblasts and in several virally or spontaneously transformed epithelial cell lines. In situ hybridizations of cultured keratinocytes supported the notion of a high level of gene expression. Indirect immunofluorescence of skin from a 19-wk fetus revealed type VII collagen gene expression at the dermal-epidermal basement membrane zone. These results indicate that several different cell types including epidermal keratinocytes and dermal fibroblasts express the type VII collagen gene, but epidermal keratinocytes may be the primary cell source of type VII collagen in developing human skin.
Similar articles
-
Transforming growth factor-beta up-regulates type VII collagen gene expression in normal and transformed epidermal keratinocytes in culture.Biochem Biophys Res Commun. 1991 Oct 31;180(2):673-80. doi: 10.1016/s0006-291x(05)81118-0. Biochem Biophys Res Commun. 1991. PMID: 1953739
-
Elevated expression of type VII collagen in the skin of patients with systemic sclerosis. Regulation by transforming growth factor-beta.J Clin Invest. 1994 Apr;93(4):1709-15. doi: 10.1172/JCI117154. J Clin Invest. 1994. PMID: 7512991 Free PMC article.
-
Normal and gene-corrected dystrophic epidermolysis bullosa fibroblasts alone can produce type VII collagen at the basement membrane zone.J Invest Dermatol. 2003 Nov;121(5):1021-8. doi: 10.1046/j.1523-1747.2003.12571.x. J Invest Dermatol. 2003. PMID: 14708601
-
The type IV collagen gene family.Contrib Nephrol. 1996;117:105-29. doi: 10.1159/000424809. Contrib Nephrol. 1996. PMID: 8801041 Review. No abstract available.
-
Sources of Collagen for Biomaterials in Skin Wound Healing.Bioengineering (Basel). 2019 Jun 30;6(3):56. doi: 10.3390/bioengineering6030056. Bioengineering (Basel). 2019. PMID: 31261996 Free PMC article. Review.
Cited by
-
CRISPR/Cas9-Mediated Generation of COL7A1-Deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa.Cell J. 2023 Oct 9;25(10):665-673. doi: 10.22074/cellj.2023.1989321.1225. Cell J. 2023. PMID: 37865875 Free PMC article.
-
Enhanced HDR-mediated correction of heterozygous COL7A1 mutations for recessive dystrophic epidermolysis bullosa.Mol Ther Nucleic Acids. 2025 Feb 1;36(1):102472. doi: 10.1016/j.omtn.2025.102472. eCollection 2025 Mar 11. Mol Ther Nucleic Acids. 2025. PMID: 40027886 Free PMC article.
-
Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.J Clin Invest. 1992 Mar;89(3):974-80. doi: 10.1172/JCI115680. J Clin Invest. 1992. PMID: 1347297 Free PMC article.
-
Dystrophic epidermolysis bullosa: a review.Clin Cosmet Investig Dermatol. 2015 May 26;8:275-84. doi: 10.2147/CCID.S54681. eCollection 2015. Clin Cosmet Investig Dermatol. 2015. PMID: 26064063 Free PMC article. Review.
-
Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids.Stem Cell Reports. 2022 Jun 14;17(6):1279-1288. doi: 10.1016/j.stemcr.2022.04.008. Epub 2022 May 12. Stem Cell Reports. 2022. PMID: 35561682 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources