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Cultivating a Three-dimensional Reconstructed Human Epidermis at a Large Scale
Published on: May 28, 2021
Immunomolecular mapping of adherens junction and desmosomal components in normal human epidermis
A Ishiko1, Y Matsunaga, T Masunaga
1Department of Dermatology, Keio University School of Medicine, Tokyo, Japan. ishiko@sc.itc.keio.ac.jp
Insights
Adherens junctions (AJs) provide distinct cell-cell adhesion in human epidermis. This study precisely maps AJs and desmosomes, revealing their unique molecular compositions and locations in keratinocytes.
Area of Science:
- Cell biology
- Dermatology
- Molecular biology
Background:
- Adherens junctions (AJs) are crucial for cell-cell and cell-matrix adhesion, linking to the actin cytoskeleton.
- Previous studies on AJ localization in human epidermis have yielded controversial results.
Purpose of the Study:
- To precisely map the molecular distribution of adherens junctions (AJs) and their components.
- To differentiate AJs from desmosomes and gap junctions in normal human epidermal keratinocytes.
Main Methods:
- Utilized electron microscopy (EM) for optimal plasma membrane fixation.
- Employed immunogold electron microscopy to localize AJ and desmosomal components.
Main Results:
- AJ structures were observed as distinct intercellular spaces, more frequent in the upper epidermis.
- E-cadherin and beta-catenin (AJ components) were absent from desmosomes but present in interdesmosomal areas.
- Plakoglobin and plakophilin 1 (desmosomal components) were localized to the desmosome's outer plaque.
Conclusions:
- Adherens junctions possess a distinct molecular composition and distribution compared to desmosomes.
- AJs and desmosomes serve as alternative cell-cell adhesion mechanisms in keratinocytes.
- AJs are regularly found between desmosomes along the keratinocyte plasma membrane.
Abstract:
Adherens junctions (AJs) are cell-cell and cell-matrix junctions that are known to comprise the transmembrane and cytoplasmic components linked to the f-actin cytoskeleton. Although the presence of AJs han been confirmed in normal human epidermis, previous studies immunolocalizing AJ-related antigens have been controversial. The purpose of this study was to produce a more precise molecular mapping of AJs and their constituents in relation to desmosomes in normal human epidermal keratinocytes. Using an electron microscope (EM) method to optimally fix plasma membranes. AJ structures were typically seen as a narrowing of the intercellular space between two keratinocytes that was distinct from desmosomes and gap junctions. Such structures were consistently found more frequently in the upper epidermis than in the basal layer. Immunogold electron microscopy showed an absence of the AJ components (E-cadherin and beta-catenin) from desmosomal areas but they were present at interdesmosomal areas at sites of close membrane association. Conversely, the desmosomal components plakoglobin and plakophilin 1 were restricted only to the outer attachment plaque of the desmosome. These results further confirm that AJs have a distinct molecular composition and distribution from desmosomes and that they regularly occur between desmosomes along the keratinocyte plasma membrane to provide alternative cell-cell adhesion mechanisms.
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