Syndecan-1, a cell-surface proteoglycan, changes in size and abundance when keratinocytes stratify
- PMID: 1401995
- DOI: 10.1111/1523-1747.ep12616103
Syndecan-1, a cell-surface proteoglycan, changes in size and abundance when keratinocytes stratify
Abstract
In epidermis, keratinocytes in the basal cell layer differentiate, lose their attachment to the underlying extracellular matrix, and form extensive intercellular adhesions as they stratify. The alterations in cell-matrix and cell-cell adhesion required for keratinocyte stratification result from changes in the expression of numerous adhesion molecules. Syndecan-1, a member of a family of cell-surface proteoglycans, is known to bind cells to interstitial matrix. Syndecan-1 localizes to specific layers of mouse epidermal keratinocytes; its expression is modest in the basal layer, heavy in the suprabasal layers, but absent from the most superficial, terminally differentiated layers. This layer-specific difference suggests that syndecan-1 expression changes with keratinocyte differentiation. To assess this hypothesis, syndecan-1 expression was evaluated before and after calcium-induced stratification and differentiation. Cells growing as an unstratified monolayer express a higher molecular mass form of syndecan-1 than do stratified cells (modal relative mass of 160 kD versus 110 kD). This structural difference is due to larger and more heparan sulfate chains on syndecan-1 from monolayer cells. In addition, the amount of cell-surface syndecan-1 changes with stratification; stratified cultures show approximately 2.5 times more syndecan-1 per cell than do unstratified cultures, but do not significantly change the level of syndecan-1-specific mRNA. Thus, the structure and amount of syndecan-1 may be regulated to meet the changing adhesive requirements of stratifying keratinocytes.
Similar articles
-
Expression of syndecan-1 is induced by differentiation and suppressed by malignant transformation of human keratinocytes.Eur J Cell Biol. 1994 Feb;63(1):43-51. Eur J Cell Biol. 1994. PMID: 8005104
-
Expression of syndecan in transformed mouse keratinocytes.Lab Invest. 1992 Aug;67(2):225-33. Lab Invest. 1992. PMID: 1501448
-
Selective changes in laminin adhesion and alpha 6 beta 4 integrin regulation are associated with the initial steps in keratinocyte maturation.Cell Growth Differ. 1996 May;7(5):615-28. Cell Growth Differ. 1996. PMID: 8732671
-
Syndecan, a developmentally regulated cell surface proteoglycan that binds extracellular matrix and growth factors.Philos Trans R Soc Lond B Biol Sci. 1990 Mar 12;327(1239):171-86. doi: 10.1098/rstb.1990.0052. Philos Trans R Soc Lond B Biol Sci. 1990. PMID: 1969657 Review.
-
Influence of cell shape and adhesiveness on stratification and terminal differentiation of human keratinocytes in culture.J Cell Sci Suppl. 1987;8:313-26. doi: 10.1242/jcs.1987.supplement_8.17. J Cell Sci Suppl. 1987. PMID: 2460477 Review.
Cited by
-
Comparison of Syndecan-1 Immunohistochemical Expression in Lobular and Ductal Breast Carcinoma with Nodal Metastases.Anal Cell Pathol (Amst). 2018 Jul 29;2018:9432375. doi: 10.1155/2018/9432375. eCollection 2018. Anal Cell Pathol (Amst). 2018. PMID: 30151336 Free PMC article.
-
Members of the syndecan family of heparan sulfate proteoglycans are expressed in distinct cell-, tissue-, and development-specific patterns.Mol Biol Cell. 1994 Jul;5(7):797-805. doi: 10.1091/mbc.5.7.797. Mol Biol Cell. 1994. PMID: 7812048 Free PMC article.
-
Epidermoid Cyst Arising in the Buccal Mucosa: Case Report and Literature Review.Acta Stomatol Croat. 2014 Dec;48(4):296-304. doi: 10.15644/asc48/4/8. Acta Stomatol Croat. 2014. PMID: 27688379 Free PMC article.
-
Proline-rich antimicrobial peptide, PR-39 gene transduction altered invasive activity and actin structure in human hepatocellular carcinoma cells.Br J Cancer. 1999 Oct;81(3):393-403. doi: 10.1038/sj.bjc.6690707. Br J Cancer. 1999. PMID: 10507762 Free PMC article.
-
Syndecan-1 - A new piece in B-cell puzzle.Pathol Oncol Res. 1997 Sep;3(3):183-91. doi: 10.1007/BF02899919. Pathol Oncol Res. 1997. PMID: 18470728
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources