Human Cord Blood-Derived Unrestricted Somatic Stem Cells Promote Wound Healing and Have Therapeutic Potential for Patients With Recessive Dystrophic Epidermolysis Bullosa

被引:34
作者
Liao, Yanling [1 ]
Itoh, Munenari [2 ]
Yang, Albert [1 ]
Zhu, Hongwen [1 ]
Roberts, Samantha [1 ]
Highet, Alexandra M. [1 ]
Latshaw, Shaun [1 ]
Mitchell, Kelly [1 ]
van de Yen, Carmella [1 ]
Christiano, Angela [3 ]
Cairo, Mitchell S. [1 ,4 ,5 ,6 ]
机构
[1] New York Med Coll, Dept Pediat, Valhalla, NY 10595 USA
[2] Jikei Univ, Dept Dermatol, Sch Med, Tokyo, Japan
[3] Columbia Univ, Dept Dermatol, Med Ctr, New York, NY 10027 USA
[4] New York Med Coll, Dept Med, Valhalla, NY 10595 USA
[5] New York Med Coll, Dept Pathol, Valhalla, NY 10595 USA
[6] New York Med Coll, Valhalla, NY 10595 USA
关键词
Skin; Stem cell transplantation; Human stem cells; Dermatology; Stem cells; Transplantation; MESENCHYMAL STROMAL CELLS; BONE-MARROW-TRANSPLANTATION; COLLAGEN GENE COL7A1; VII COLLAGEN; SKIN; DIFFERENTIATION; EXPRESSION; GENERATION; CONTRIBUTE; MODEL;
D O I
10.3727/096368913X663569
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human umbilical cord blood (CB)-derived unrestricted somatic stem cells (USSCs) have previously been demonstrated to have a broad differentiation potential and regenerative beneficial effects when administered in animal models of multiple degenerative diseases. Here we demonstrated that USSCs could be induced to express genes that hallmark keratinocyte differentiation. We also demonstrated that USSCs express type VII collagen (C7), a protein that is absent or defective in patients with an inherited skin disease, recessive dystrophic epidermolysis bullosa (RDEB). In mice with full-thickness excisional wounds, a single intradermal injection of USSCs at a 1-cm distance to the wound edge resulted in significantly accelerated wound healing. USSC-treated wounds displayed a higher density of CD31(+) cells, and the wounds healed with a significant increase in skin appendages. These beneficial effects were demonstrated without apparent differentiation of the injected USSCs into keratinocytes or endothelial cells. In vivo bioluminescent imaging (BLI) revealed specific migration of USSCs modified with a luciferase reporter gene, from a distant intradermal injection site to the wound, as well as following systemic injection of USSCs. These data suggest that CB-derived USSCs could significantly contribute to wound repair and be potentially used in cell therapy for patients with RDEB.
引用
收藏
页码:303 / 317
页数:15
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