Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/828
Title: Lamellation in fibrous dysplasia: a clinicopathologic study
Authors: Çiçek, Ali Fuat
Kılınç, Melih
Safalı, Mükerrem
Günhan, Ömer
Günhan, Ömer [9402]
Keywords: Human skin graft, Pressure ulcers, Wound healing, Dermal scaffold, Fibrillin-microfibrils components
Issue Date: Sep-2018
Publisher: F Hernandez
Source: Cicek, A. F., Kilinc, M., Safali, M., & Gunhan, O. (2018). Lamellation in fibrous dysplasia: A clinicopathologic study. Histology and histopathology, 33(9), 971-977.
Abstract: Despite advances in regenerative medicine and tissue engineering, human skin substitutes remain a clear goal to achieve. Autografts remain the principal clinical option. The long-term changes in dermis, as well as its response after injuries, are not well known. Research in this field has been hindered by a lack of experimental animal models. This study analyzes the architectural dermal scaffold (collagen and elastin fibers plus fibrillin-microfibrils) changes in a model of human skin pressure ulcers in mice. Immunosuppressed NOD/Scid mice (n=10) were engrafted with human skin of dimensions 4x3 cm. After 60 days as a permanent graft, a pressure ulcer (PU) was created in the human skin using a compression device. Three study groups were established: full-thickness skin graft before (hFTSG) and after applying mechanical pressure (hFTSG-PU). Native human skin was used as control group. Evaluations were conducted with visual and histological assessment. Scaffold components from each group were compared by immunohistochemical staining (tropoelastin, collagen I and III, metalloproteins (MMP), fibulins, and lysil oxidases (LOX) among others). The long-term engrafted skin showed a certain degradative state of dermis scaffold, as noticed by the active expression of MMPs and tropoelastin compared to native skin. However, a great reparative response after pressure ulcer onto the engrafted skin was observed. A significant increase of fibrillin microfibrils components (TGF-β, MAGP-1 and fibrillin-1), and matrix suprastructures of collagen I, III and LOX lead to an active restructuration of dermal tissue. Our human skin model in mice revealed the important role of the dermal scaffold component to reach skin stability and its capability to react to mechanical pressure injuries. These results showed the important role of dermal scaffold to support the histoarchitecture and mechanosensation of the human skin.
Description: Offprint requests to: Melih Kilinc, MD, Gulhane Training and Research Hospital, Department of Pathology, 06010 Ankara Turkey. e-mail: drmelihkilinc@gmail.com
URI: https://hdl.handle.net/20.500.11851/828
http://www.hh.um.es/Abstracts/Vol_33/33_9/33_9_971.htm
Appears in Collections:Cerrahi Tıp Bilimleri Bölümü / Department of Surgical Sciences
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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