Abstract

The epidermis functions in skin as first defense line or barrier against environmental impacts, resting on extracellular matrix (ECM) of the dermis underneath. Both compartments are connected by the basement membrane (BM), composed of a set of distinct glycoproteins and proteoglycans. Herein we are reviewing molecular aspects of BM structure, composition, and function regarding not only (i) the dermoepidermal interface but also (ii) the resident microvasculature, primarily focusing on the per se nonscaffold forming components perlecan and nidogen-1 and nidogen-2. Depletion or functional deficiencies of any BM component are lethal at some stage of development or around birth, though BM defects vary between organs and tissues. Lethality problems were overcome by developmental stage- and skin-specific gene targeting or by cell grafting and organotypic (3D) cocultures of normal or defective cells, which allows recapitulating BM formation de novo. Thus, evidence is accumulating that BM assembly and turnover rely on mechanical properties and composition of the adjacent ECM and the dynamics of molecular assembly, including further “minor” local components, nidogens largely functioning as catalysts or molecular adaptors and perlecan as bridging stabilizer. Collectively, orchestration of BM assembly, remodeling, and the role of individual players herein are determined by the developmental, tissue-specific, or functional context.

Highlights

  • In skin the epidermis represents the outer barrier of the organism, providing protection against physical, chemical, and microbial impacts of the environment

  • Evidence is accumulating that basement membrane (BM) assembly and turnover rely on mechanical properties and composition of the adjacent extracellular matrix (ECM) and the dynamics of molecular assembly, including further “minor” local components, nidogens largely functioning as catalysts or molecular adaptors and perlecan as bridging stabilizer

  • The striking differences between dermoepidermal BM formation in situ and in 3D cocultures indicate that tissuerelated molecular modifications or “minor” components may play a role in addition to chemical and mechanical properties of the dermal ECM

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Summary

Introduction

In skin the epidermis represents the outer barrier of the organism, providing protection against physical, chemical, and microbial impacts of the environment. It should be mentioned beforehand that skin in general is serving multiple other functions (e.g., sensing touch, pain, temperature, and priming immune responses), representing our second largest organ only surpassed by the vascular system. BioMed Research International the two compartments rendering primarily a stabilizing, though still dynamic interface and a diffusion barrier [12,13,14,15,16,17,18,19] Besides their prominence in skin, BMs support all epithelia and endothelia, enwrap Schwann cells and nerve extensions [20, 21], muscles [22, 23], tissue compartments like fat, and whole organs [14]. Particular properties or microheterogeneity of BMs is supposed to contribute to the niche of tissue-specific stem or progenitor cells [66,67,68,69,70,71,72]

Molecular Building Blocks of Basement Membranes
Identification of Molecular BM Defects by Genetic Approaches
Human Cells Rebuild Epidermal Architecture in Mouse Xenografts
Nidogen Plays an Essential Role for BM Assembly In Vitro
Cutaneous Microvasculature Is More Severely Affected by Molecular BM Defects
Findings
10. Summary and Further Outlook
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