31
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Tissue-engineered human skin substitutes developed from collagen-populated hydrated gels: clinical and fundamental applications.

      Medical & Biological Engineering & Computing
      Cell Culture Techniques, methods, Collagen, Gels, Humans, Skin, Artificial, Wound Healing

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The field of tissue engineering has opened several avenues in biomedical sciences, through ongoing progress. Skin substitutes are currently optimised for clinical as well as fundamental applications. The paper reviews the development of collagen-populated hydrated gels for their eventual use as a therapeutic option for the treatment of burn patients or chronic wounds: tools for pharmacological and toxicological studies, and cutaneous models for in vitro studies. These skin substitutes are produced by culturing keratinocytes on a matured dermal equivalent composed of fibroblasts included in a collagen gel. New biotechnological approaches have been developed to prevent contraction (anchoring devices) and promote epithelial cell differentiation. The impact of dermo-epidermal interactions on the differentiation and organisation of bio-engineered skin tissues has been demonstrated with human skin cells. Human skin substitutes have been adapted for percutaneous absorption studies and toxicity assessment. The evolution of these human skin substitutes has been monitored in vivo in preclinical studies showing promising results. These substitutes could also serve as in vitro models for better understanding of the immunological response and healing mechanism in human skin. Thus, such human skin substitutes present various advantages and are leading to the development of other bio-engineered tissues, such as blood vessels, ligaments and bronchi.

          Related collections

          Most cited references71

          • Record: found
          • Abstract: not found
          • Article: not found

          The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Matrix metalloproteinases and their inhibitors in connective tissue remodeling.

            Matrix metalloproteinases are an important group of zinc enzymes responsible for degradation of the extracellular matrix components such as collagen and proteoglycans in normal embryogenesis and remodeling and in many disease processes such as arthritis, cancer, periodontitis, and osteoporosis. A matrixin family is defined, comprising at least seven members that range in size from Mr 28,000 to 92,000 and are related in gene sequence to collagenase. All family members are secreted as zymogens that lose peptides of about 10,000 daltons upon activation. Latency is due to a conserved cysteine that binds to zinc at the active center. Latency is overcome by physical (chaotropic agents), chemical (HOCl, mercurials), and enzymatic (trypsin, plasmin) treatments that separate the cysteine residue from the zinc. Expression of the metalloproteinases is switched on by a variety of agents acting through regulatory elements of the gene, particularly the AP-1 binding site. A family of protein inhibitors of Mr 28,500 or less binds strongly and stoichiometrically in noncovalent fashion to inhibit members of the family. The serum protein alpha 2-macroglobulin and relatives are also strongly inhibitory.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Presence of modified fibroblasts in granulation tissue and their possible role in wound contraction.

                Bookmark

                Author and article information

                Journal
                10367474
                10.1007/BF02518887

                Chemistry
                Cell Culture Techniques,methods,Collagen,Gels,Humans,Skin, Artificial,Wound Healing
                Chemistry
                Cell Culture Techniques, methods, Collagen, Gels, Humans, Skin, Artificial, Wound Healing

                Comments

                Comment on this article