Deep dermal fibroblast profibrotic characteristics are enhanced by bone marrow-derived mesenchymal stem cells

• Published in: Wound repair and regeneration Vol. 21; no. 3; pp. 448 - 455
• Main Authors: Ding, Jie, Ma, Zengshuan, Shankowsky, Heather A., Medina, Abelardo, Tredget, Edward E.
• Format: Journal Article
• Language: English
• Published: United States Blackwell Publishing Ltd 01.05.2013
• Subjects: Adult; Burns - metabolism; Burns - pathology; Burns - surgery; Cell Proliferation; Cells, Cultured; Cicatrix, Hypertrophic - metabolism; Cicatrix, Hypertrophic - pathology; Cicatrix, Hypertrophic - prevention & control; Collagen - biosynthesis; Collagen - genetics; Female; Fibroblasts - metabolism; Fibroblasts - pathology; Gene Expression Regulation; Humans; Laser-Doppler Flowmetry; Male; Mesenchymal Stromal Cells; Middle Aged; Real-Time Polymerase Chain Reaction; RNA, Messenger - genetics; Skin - metabolism; Skin - pathology; Stem Cell Transplantation - methods; Wound Healing - physiology
• ISSN: 1067-1927; 1524-475X; 1524-475X
• DOI: 10.1111/wrr.12046

Hypertrophic scars are a significant fibroproliferative disorder complicating deep injuries to the skin. We hypothesize that activated deep dermal fibroblasts are subject to regulation by bone marrow–derived mesenchymal stem cells (BM‐MSCs), which leads to the development of excessive fibrosis following deep dermal injury. We found that the expression of fibrotic factors was higher in deep burn wounds compared with superficial burn wounds collected from burn patients with varying depth of skin injury. We characterized deep and superficial dermal fibroblasts, which were cultured from the deep and superficial dermal layers of normal uninjured skin obtained from abdominoplasty patients, and examined the paracrine effects of BM‐MSCs on the fibrotic activities of the cells. In vitro, deep dermal fibroblasts were found higher in the messenger RNA (mRNA) levels of type 1 collagen, alpha smooth muscle actin, transforming growth factor beta, stromal cell–derived factor 1, and tissue inhibitor of metalloproteinase 1, an inhibitor of collagenase (matrix metalloproteinase 1). As well, deep dermal fibroblasts had low matrix metalloproteinase 1 mRNA, produced more collagen, and contracted collagen lattices significantly greater than superficial fibroblasts. By co‐culturing layered fibroblasts with BM‐MSCs in a transwell insert system, BM‐MSCs enhanced the fibrotic behavior of deep dermal fibroblasts, which suggests a possible involvement of BM‐MSCs in the pathogenesis of hypertrophic scarring.