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Previous chronic exogenous glucocorticoid administration in vivo does not affect functional characteristics and cellular lifespan of human skin fibroblasts in vitro
Author(s) -
Pratsinis Harris,
Dimozi Anastasia,
Pilichos Konstantinos,
Tsagarakis Stylianos,
Yiacoumettis Andreas M,
Kletsas Dimitris
Publication year - 2011
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2011.01262.x
Subject(s) - in vivo , glucocorticoid , human skin , fibroblast , homeostasis , in vitro , wound healing , skin aging , endocrinology , medicine , physiology , biology , pharmacology , immunology , dermatology , biochemistry , genetics , microbiology and biotechnology
Abstract: Excess of glucocorticoids (GCs) has been reported to lead to skin atrophy and impaired wound healing. The present study investigates whether human skin fibroblasts suffer permanent damages due to a long‐term exposure to GC excess. Fibroblasts obtained from patients being under GC treatment for periods over one year were cultured under standard conditions in vitro, and studied regarding pivotal parameters involved in skin homeostasis and aging, i.e. collagen production, cell proliferation, and cellular replicative lifespan. No statistical differences were observed regarding these functions compared to those of normal human skin fibroblasts. Furthermore, no differences between normal and patient‐derived cells were observed regarding their sensitivity to a supra‐physiological cortisol concentration. In conclusion, the prolonged exposure of human skin fibroblasts in vivo to high concentrations of exogenously‐administered GC does not lead to persistent adverse effects on their physiology.