Allogeneic Transplantation of an Adipose-Derived Stem Cell Sheet Combined With Artificial Skin Accelerates Wound Healing in a Rat Wound Model of Type 2 Diabetes and Obesity

被引:159
作者
Kato, Yuka [1 ,2 ]
Iwata, Takanori [2 ]
Morikawa, Shunichi [3 ]
Yamato, Masayuki [2 ]
Okano, Teruo [2 ]
Uchigata, Yasuko [1 ]
机构
[1] Tokyo Womens Med Univ, Sch Med, Diabet Ctr, Tokyo, Japan
[2] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Tokyo, Japan
[3] Tokyo Womens Med Univ, Sch Med, Dept Anat & Dev Biol, Tokyo, Japan
关键词
FIBROBLAST-GROWTH-FACTOR; STROMAL CELLS; BONE-MARROW; IN-VIVO; POSTNATAL NEOVASCULARIZATION; STEM/STROMAL CELLS; ENDOTHELIAL-CELLS; BLOOD-VESSELS; FOOT ULCERS; TISSUE;
D O I
10.2337/db14-1133
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
One of the most common complications of diabetes is diabetic foot ulcer. Diabetic ulcers do not heal easily due to diabetic neuropathy and reduced blood flow, and nonhealing ulcers may progress to gangrene, which necessitates amputation of the patient's foot. This study attempted to develop a new cell-based therapy for nonhealing diabetic ulcers using a full-thickness skin defect in a rat model of type 2 diabetes and obesity. Allogeneic adipose-derived stem cells (ASCs) were harvested from the inguinal fat of normal rats, and ASC sheets were created using cell sheet technology and transplanted into full-thickness skin defects in Zucker diabetic fatty rats. The results indicate that the transplantation of ASC sheets combined with artificial skin accelerated wound healing and vascularization, with significant differences observed 2 weeks after treatment. The ASC sheets secreted large amounts of several angiogenic growth factors in vitro, and transplanted ASCs were observed in perivascular regions and incorporated into the newly constructed vessel structures in vivo. These results suggest that ASC sheets accelerate wound healing both directly and indirectly in this diabetic wound-healing model. In conclusion, allogeneic ASC sheets exhibit potential as a new therapeutic strategy for the treatment of diabetic ulcers.
引用
收藏
页码:2723 / 2734
页数:12
相关论文
共 60 条
[1]  
Aguirre F., 2013, IDF DIABETES ATLAS
[2]   Rolling circle amplification: a versatile tool for chemical biology, materials science and medicine [J].
Ali, M. Monsur ;
Li, Feng ;
Zhang, Zhiqing ;
Zhang, Kaixiang ;
Kang, Dong-Ku ;
Ankrum, James A. ;
Le, X. Chris ;
Zhao, Weian .
CHEMICAL SOCIETY REVIEWS, 2014, 43 (10) :3324-3341
[3]   VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[4]   Growth factors and cytokines in wound healing [J].
Barrientos, Stephan ;
Stojadinovic, Olivera ;
Golinko, Michael S. ;
Brem, Harold ;
Tomic-Canic, Marjana .
WOUND REPAIR AND REGENERATION, 2008, 16 (05) :585-601
[5]   The role of stem cells in the treatment of diabetic foot ulcers [J].
Blumberg, Sheila N. ;
Berger, Alexandra ;
Hwang, Lisa ;
Pastar, Irena ;
Warren, Stephen M. ;
Chen, Weiliam .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2012, 96 (01) :1-9
[6]   The global burden of diabetic foot disease [J].
Boulton, AJM ;
Vileikyte, L ;
Ragnarson-Tennvall, G ;
Apelqvist, J .
LANCET, 2005, 366 (9498) :1719-1724
[7]   Cellular and molecular basis of wound healing in diabetes [J].
Brem, Harold ;
Tomic-Canic, Marjana .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (05) :1219-1222
[8]   The allogeneic response to cultured human skin equivalent in the hu-PBL-SCID mouse model of skin rejection [J].
Briscoe, DM ;
Dharnidharka, VR ;
Isaacs, C ;
Downing, G ;
Prosky, S ;
Shaw, P ;
Parenteau, NL ;
Hardin-Young, J .
TRANSPLANTATION, 1999, 67 (12) :1590-1599
[9]   Human adipose tissue-derived stem cells differentiate into endothelial cells in vitro and improve postnatal neovascularization in vivo [J].
Cao, Y ;
Sun, Z ;
Liao, LM ;
Meng, Y ;
Han, Q ;
Zhao, RCH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 332 (02) :370-379
[10]  
Casteilla Louis, 2011, World J Stem Cells, V3, P25, DOI 10.4252/wjsc.v3.i4.25