Cel A BETTER UNDERSTANDING OF THE RELATIONSHIP BETWEEN BIOLOGICAL AND BIOMECHANICAL PROPERTIES OF THE RECONSTRUCTED TISSUE COULD OPEN ALSO A NEW FIELD FOR EVALUATING TOXICOLOGICAL AND PHARMACOLOGICAL PROPERTIES. The model enabled the study of the regulation of cell density in a tissue, the influence of the substrate on attachment, proliferation and protein synthesis, and collagen and collagenase gene expression in fibroblasts at a transcriptional or pretranslational level. The dermal equivalent is a model for skin ageing, wound contraction and studies on pathological fibroblasts. The covering of the dermal equivalent by an epidermis leads to models of epidermal wound healing, pigmentation and epidermal ageing. In addition, dermal epidermal interactions can be investigated. This human living skin equivalent, in which cells communicate and differentiate as in vivo is a major tool for pharmacotoxicology. It enables the identification of the influence of cell cell, cell matrix and dermal epidermal interactions in response to pharmacological agents. A human dermal equivalent model has been developed by culturing cells in close contact with their physiological matrix molecules and with cell types usually adjacent in vivo.CELLS AND CONNECTIVE TISSUE COMPONENTS FROM THE SKIN CAN BE ISOLATED AND INVESTIGATED SEPARATELY IN DIFFERENT ORGAN AND CELL CULTURE. THE INDIVIDUAL CONSTITUENTS CAN ALSO BE USED TO RECONSTITUTE IN VITRO A SKIN EQUIVALENT.THE RECONSTITUTION OF AN ARTIFICAL DERMIS REQUIRES TWO MAJOR COMPONENTS : FIBROBLASTS AND CONNECTIVE TISSUE MATRIX.IN THIS MODEL, THE DIFFERENTIATION OF FIBROBLASTS BECOME SIMILAR TO THE IN VIVO SITUATION AND QUITE DIFFERENT FROM FIBROBLASTS CULTIVATED AS MONOLAYERS, WHICH ARE USUALLY USED FOR PHARMACOLOGICAL OR TOXICOLOGICAL STUDIES. IT IS PROPOSED TO INVESTIGATED THE BASIC CELLULAR AND CELL MATRIX INTERACTIONS EXPRESSED IN THIS MODEL, AS COMPARED WITH IN VIVO CONDITIONS AND OTHER IN VITRO CULTURE SYSTEMS, AND TO EVALUATE THE POTENTIALITY OF THIS MODEL FOR TOXICOLOGICAL AND PHARMACOLOGICAL STUDIES. Dziedzina nauki natural sciencesbiological sciencesbiochemistrybiomoleculesproteins Program(-y) FP1-BAP - Multiannual research action programme (EEC) in the field of biotechnology (BAP), 1985-1989 Temat(-y) Data not available Zaproszenie do składania wniosków Data not available System finansowania CSC - Cost-sharing contracts Koordynator St Thomas's Hospital Medical School Wkład UE Brak danych Adres Lambeth Palace Road London Zjednoczone Królestwo Zobacz na mapie Koszt całkowity Brak danych Uczestnicy (4) Sortuj alfabetycznie Sortuj według wkładu UE Rozwiń wszystko Zwiń wszystko Hôpital Henri Mondor Francja Wkład UE Brak danych Adres 94010 Créteil Zobacz na mapie Koszt całkowity Brak danych LUDWIG-MAXIMILIANS UNIVERSITY OF MUNICH Niemcy Wkład UE Brak danych Adres Geschwister-Scholl-Platz 1 80539 MUENCHEN Zobacz na mapie Koszt całkowity Brak danych UNIVERSITE DE LIEGE Belgia Wkład UE Brak danych Adres LAPIERE C M Zobacz na mapie Koszt całkowity Brak danych University of Wales College of Medicine Zjednoczone Królestwo Wkład UE Brak danych Adres Heath Park CF4 4XN Cardiff Zobacz na mapie Koszt całkowity Brak danych
