A Comparative Quantitative Analysis of Laminin-5 in the Basement Membrane of Normal, Hyperplastic, and Malignant Oral Mucosa by Confocal Immunofluorescence Imaging
Open Access
- 1 October 2001
- journal article
- research article
- Published by SAGE Publications in Journal of Histochemistry & Cytochemistry
- Vol. 49 (10) , 1261-1268
- https://doi.org/10.1177/002215540104901008
Abstract
Laminin-5 (Ln-5) is a heterotrimeric basement membrane (BM) molecule (α3β3γ2). It is a principal protein constituent of the anchoring filaments, which connect the BM with the hemidesmosomes of the basal keratinocytes and possess a crucial function in keratinocyte adhesion. Confocal immunofluorescence imaging is introduced for a quantitative evaluation of the Ln-5 content in the BM of oral squamous epithelium. The BM of normal oral mucosa was used as a reference (100%) for comparative analysis and showed a nearly uniform Ln-5 immunofluorescence intensity (99–100%). In all hyperplastic lesions of oral mucosa, the Ln-5 immunofluorescence intensity was increased (107–141%). The increased Ln-5 content in the BM of hyperplastic lesions suggests an increased keratinocyte-BM adhesion, possibly resulting in a higher stability of the oral mucosa. In contrast, in the oral squamous cell carcinoma (OSCC) invasive front, the remaining BM segments were characterized by a decrease in Ln-5 immunofluorescence intensity (35–74%). A stronger decrease of Ln-5-linked kerationocyte-BM adhesion correlates with a higher tumor grade. Because in central areas of carcinoma BM segments with a normal Ln-5 content could be demonstrated, the fundamental Ln-5 diminution in BM segments of the invasive front should be considered as an invasion-associated phenomenon.Keywords
This publication has 37 references indexed in Scilit:
- Quantitative immunoelectron microscopy of type VI collagen in glomeruli in type I diabetic patientsKidney International, 2001
- Isolation and Activity of Proteolytic Fragment of Laminin-5 α3 ChainBiochemical and Biophysical Research Communications, 2000
- Tumor cell budding and laminin-5 expression in colorectal carcinoma can be modulated by the tissue micro-environmentInternational Journal of Cancer, 2000
- Altered distribution and synthesis of laminin-5 (kalinin) in oral lichen planus, epithelial dysplasias and squamous cell carcinomasBritish Journal of Dermatology, 1997
- γ2 Chain of Laminin-5 Is Recognized By Monoclonal Antibody GB3Journal of Investigative Dermatology, 1995
- Analysis of antifading reagents for fluorescence microscopyCytometry, 1995
- Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches.The Journal of cell biology, 1994
- The dermal-epidermal junction of human skin contains a novel laminin variant.The Journal of cell biology, 1992
- Heterogeneity of basement membranes in normal and pathologically altered tissuesVirchows Archiv, 1990
- Normal epithelial antigens recognized by GB3 and GB5 are diminished in intraductal and lost in infiltrating human breast carcinomasBreast Cancer Research and Treatment, 1986