Bone Marrow-Derived Stromal Cells (BMSCs) Interact with Fibroblasts in Accelerating Wound Healing

被引:16
作者
Dulchavsky, Deborah [1 ]
Gao, Xiaohua [1 ]
Liu, Yong Bo [1 ]
Deeb, Dorrah [1 ]
Arbab, Ali S. [2 ]
McIntosh, Kevin [3 ]
Dulchavsky, Scott A. [1 ]
Gautam, Subhash C. [1 ]
机构
[1] Henry Ford Hlth Syst, Dept Gen Surg, Detroit, MI USA
[2] Henry Ford Hlth Syst, Dept Diagnost Radiol, Detroit, MI USA
[3] Cognate BioServ, Baltimore, MD USA
关键词
wound healing; mesenchymal stem cells; fibroblasts; wound closure; cell migration;
D O I
10.1080/08941930802216831
中图分类号
R61 [外科手术学];
学科分类号
摘要
Bone marrow-derived stromal cells (BMSCs) exhibit extraordinary degree of plasticity and growth factor repertoire for which they have been investigated for repair and regeneration of damaged tissues, but have not been adequately examined for wound healing. The ability of BMSCs to accelerate healing of surgically inflicted cutaneous and fascial wounds was tested in vivo in rats and in vitro using a fibroblast monolayer wound model. Intravenous treatment with BMSCs augmented healing of both cutaneous and fascial wounds as determined by an increase in the biomechanical strength of wounds. In vitro experiments showed that incorporation of BMSCs in fibroblast monolayers accelerates the closure of mechanically disrupted monolayers, which was attributed to the enhanced migration of fibroblasts onto the denuded surfaces. Furthermore, culture medium conditioned by activated BMSCs promoted the closure of defects in monolayers and enhanced the proliferation/growth and directional migration (chemotaxis) of fibroblasts. This study demonstrates that BMSCs significantly augment healing of cutaneous and fascial wounds in vivo at least in part through interaction with fibroblasts in which BMSCs promote growth and chemotaxis of fibroblasts.
引用
收藏
页码:270 / 279
页数:10
相关论文
共 37 条
[31]  
Steed DL, 1998, CLIN PLAST SURG, V25, P397
[32]  
Steeper R, 2005, J Wound Care, V14, P101
[33]   Hepatocyte growth factor is constitutively produced by human bone marrow stromal cells and indirectly promotes hematopoiesis [J].
Takai, K ;
Hara, J ;
Matsumoto, K ;
Hosoi, G ;
Osugi, Y ;
Tawa, A ;
Okada, S ;
Nakamura, T .
BLOOD, 1997, 89 (05) :1560-1565
[34]   Suppression of allogeneic T-cell proliferation by human marrow stromal cells: Implications in transplantation [J].
Tse, WT ;
Pendleton, JD ;
Beyer, WM ;
Egalka, MC ;
Guinan, EC .
TRANSPLANTATION, 2003, 75 (03) :389-397
[35]   Bone marrow cells differentiate into wound myofibroblasts and accelerate the healing of wounds with exposed bones when combined with an occlusive dressing [J].
Yamaguchi, Y ;
Kubo, T ;
Murakami, T ;
Takahashi, M ;
Hakamata, Y ;
Kobayashi, E ;
Yoshida, S ;
Hosokawa, K ;
Yoshikawa, K ;
Itami, S .
BRITISH JOURNAL OF DERMATOLOGY, 2005, 152 (04) :616-622
[36]   Myocardial regeneration with bone-marrow-derived stem cells [J].
Yoon, YS ;
Lee, N ;
Scadova, H .
BIOLOGY OF THE CELL, 2005, 97 (04) :253-263
[37]   Healing times and prediction of wound healing in neuropathic diabetic foot ulcers: a prospective study [J].
Zimny, S ;
Pfohl, M .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2005, 113 (02) :90-93