Adipose derived mesenchymal stem cells improve diabetic wound healing in mouse animal model: extracellular matrix remodeling maybe a potential therapeutic usage of stem cells.

被引:0
作者
Ghaneialvar, Hori [1 ]
Lotfi, Abbas Sahebghadam [1 ]
Arjmand, Sareh [2 ]
Soleimani, Masoud [3 ]
Abbas, Fatemeh Mashhadi [4 ]
机构
[1] Tarbiat Modares Univ, Dept Clin Biochem, Fac Med Sci, Tehran, Iran
[2] Shahid Beheshti Univ, Prot Res Ctr, Tehran, Iran
[3] Tarbiat Modares Univ, Dept Hematol, Fac Med Sci, Tehran, Iran
[4] Shaheed Beheshti Univ Med Sci, Sch Dent, Dept Oral Pathol, Tehran, Iran
来源
BIOMEDICAL RESEARCH-INDIA | 2017年 / 28卷 / 08期
关键词
Adult stem cells; Wound healing; Extracellular matrix; Matrix metalloproteinase; TISSUE INHIBITORS; STROMAL CELLS; METALLOPROTEINASES; EXPRESSION; UPA; OVEREXPRESSION; MICRORNAS; PROTEASES; TIMP-1;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Skin wounds cause damage to the body's first layer of protection. This, disclosed a person to further injury. Wounds normally heal in a very orderly and efficient process. However, activation of this efficient process is sometimes lost in pathologic conditions such as diabetes. The objective of the present study was to evaluate the expression of some genes in Adipose Derived Mesenchymal Stem Cells (ADSCs) that were used for the healing of the diabetic wound of mouse. ADSCs were separated from adipose tissue of mice, confirmed by surface markers CD34, CD105, CD44 and bone or fat cells differentiation. Then 10 x 105 stem cells were immediately injected in four areas around the wound that previously were created on the dorsal skin of each diabetic mouse. TIMP-1, MMP-2, MMP-9 and uPA genes expression folds in the wound area were examined on 3rd, 7th, 14th and 21st days, using q-PCR. Three groups' mice were evaluated: non-diabetic, diabetic without any treatment and diabetic with ADSCs treatment. The expression level of uPA and MMP-9 genes were decreased in the stem cell-treated group but TIMP1 and MMP2 genes folds were increased significantly (p<0.05) compared to the diabetes group without any treatment. The results of this study suggest that stem cell transplantation maybe applicable in diabetic wounds healing via changing the content of tissue gene expressions.
引用
收藏
页码:3672 / 3679
页数:8
相关论文
共 54 条
[1]   Adipose-Derived Mesenchymal Stromal/Stem Cells: Tissue Localization, Characterization, and Heterogeneity [J].
Baer, Patrick C. ;
Geiger, Helmut .
STEM CELLS INTERNATIONAL, 2012, 2012
[2]   Mesenchymal stem cell-derived IL-10 and recovery from infarction - A third pitch for the chord [J].
Bishopric, Nanette H. .
CIRCULATION RESEARCH, 2008, 103 (02) :125-127
[3]   The tissue inhibitors of metalloproteinases (TIMPs): An ancient family with structural and functional diversity [J].
Brew, Keith ;
Nagase, Hideaki .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2010, 1803 (01) :55-71
[4]   Stem cells in cutaneous wound healing [J].
Cha, Jisun ;
Falanga, Vincent .
CLINICS IN DERMATOLOGY, 2007, 25 (01) :73-78
[5]   Therapeutic potential of bone marrow-derived mesenchymal stem cells for cutaneous wound healing [J].
Chen, Jerry S. ;
Wong, Victor W. ;
Gurtner, Geoffrey C. .
FRONTIERS IN IMMUNOLOGY, 2012, 3
[6]  
Collier Mark, 2003, Nurs Times, V99, P63
[7]   Apoptosis is increased in a model of diabetes-impaired wound healing in genetically diabetic mice [J].
Darby, IA ;
Bisucci, T ;
Hewitson, TD ;
MacLellan, DG .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1997, 29 (01) :191-200
[8]   MicroRNA-122 Overexpression Promotes Hepatic Differentiation of Human Adipose Tissue-Derived Stem Cells [J].
Davoodian, Nahid ;
Lotfi, Abbas S. ;
Soleimani, Masoud ;
Mowla, Seyed Javad .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2014, 115 (09) :1582-1593
[9]   Wound healing: An overview of acute, fibrotic and delayed healing [J].
Diegelmann, RF ;
Evans, MC .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :283-289
[10]   Stem Cells in Wound Healing: The Future of Regenerative Medicine? A Mini-Review [J].
Duscher, Dominik ;
Barrera, Janos ;
Wong, Victor W. ;
Maan, Zeshaan N. ;
Whittam, Alexander J. ;
Januszyk, Michael ;
Gurtner, Geoffrey C. .
GERONTOLOGY, 2016, 62 (02) :216-225