Therapeutic potential of gingival fibroblasts for cutaneous radiation syndrome: comparison to bone marrow-mesenchymal stem cell grafts

• Published in: Stem cells and development Vol. 24; no. 10; p. 1182
• Main Authors: Linard, Christine, Tissedre, Frederique, Busson, Elodie, Holler, Valerie, Leclerc, Thomas, Strup-Perrot, Carine, Couty, Ludovic, L'homme, Bruno, Benderitter, Marc, Lafont, Antoine, Lataillade, Jean Jacques, Coulomb, Bernard
• Format: Journal Article
• Language: English
• Published: United States 15.05.2015
• Subjects: Animals; Bone Marrow - metabolism; Bone Marrow Cells - cytology; Cell Differentiation - physiology; Fibroblasts - cytology; Humans; Mesenchymal Stem Cell Transplantation - methods; Mesenchymal Stromal Cells - cytology; Mice, SCID; Radiation Injuries - metabolism; Radiation Injuries - pathology; Skin - injuries; Skin - pathology; Wound Healing - physiology
• ISSN: 1557-8534
• DOI: 10.1089/scd.2014.0486

Mesenchymal stem cell (MSC) therapy has recently been investigated as a potential treatment for cutaneous radiation burns. We tested the hypothesis that injection of local gingival fibroblasts (GFs) would promote healing of radiation burn lesions and compared results with those for MSC transplantation. Human clinical- grade GFs or bone marrow-derived MSCs were intradermally injected into mice 21 days after local leg irradiation. Immunostaining and real-time PCR analysis were used to assess the effects of each treatment on extracellular matrix remodeling and inflammation in skin on days 28 and 50 postirradiation. GFs induced the early development of thick, fully regenerated epidermis, skin appendages, and hair follicles, earlier than MSCs did. The acceleration of wound healing by GFs involved rearrangement of the deposited collagen, modification of the Col/MMP/TIMP balance, and modulation of the expression and localization of tenascin-C and of the expression of growth factors (VEGF, EGF, and FGF7). As MSC treatment did, GF injection decreased the irradiation-induced inflammatory response and switched the differentiation of macrophages toward an M2-like phenotype, characterized by CD163(+) macrophage infiltration and strong expression of arginase-1. These findings indicate that GFs are an attractive target for regenerative medicine, for easier to collect, can grow in culture, and promote cutaneous wound healing in irradiation burn lesions.