Transplantation of bone marrow mesenchymal stem cells on collagen scaffolds for the functional regeneration of injured rat uterus

被引:195
作者
Ding, Lijun [1 ,2 ]
Li, Xin'an [3 ]
Sun, Haixiang [1 ]
Su, Jing [3 ]
Lin, Nacheng [3 ]
Peault, Bruno [4 ]
Song, Tianran [3 ]
Yang, Jun [5 ]
Dai, Jianwu [2 ,6 ]
Hu, Yali [1 ,2 ,3 ]
机构
[1] Nanjing Univ, Dept Obstet & Gynecol, Sch Med, Ctr Reprod Med,Affiliated Drum Tower Hosp, Nanjing 210008, Jiangsu, Peoples R China
[2] Nanjing Univ, Nanjing Ctr Stem Cells & Biomat, Sch Med, Affiliated Drum Tower Hosp, Nanjing 210008, Jiangsu, Peoples R China
[3] Nanjing Univ, Dept Obstet & Gynecol, Sch Med, Affiliated Drum Tower Hosp, Nanjing 210008, Jiangsu, Peoples R China
[4] Univ Edinburgh, Ctr Regenerat Med, Edinburgh EH16 4UU, Midlothian, Scotland
[5] Nanjing Univ, Dept Pathol, Sch Med, Nanjing Drum Tower Hosp, Nanjing 210008, Jiangsu, Peoples R China
[6] Chinese Acad Sci, Inst Genet & Dev Biol, Beijing 100190, Peoples R China
关键词
Uterine regeneration; Collagen scaffold; Bone marrow-derived mesenchymal stem; cells; Microvasculature; ENDOTHELIAL GROWTH-FACTOR; STROMAL CELLS; ENDOMETRIUM; BIOLOGY; DIFFERENTIATION; IDENTIFICATION; PROGENITORS; MECHANISMS; PREVENTION; POPULATION;
D O I
10.1016/j.biomaterials.2014.02.046
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Serious injuries of endometrium in women of reproductive age are often followed by uterine scar formation and a lack of functional endometrium predisposing to infertility or miscarriage. Bone marrowderived mesenchymal stem cells (BM-MSCs) have shown great promise in clinical applications. In the present study, BM-MSCs loaded onto degradable collagen membranes were constructed. Collagen membranes provided 3-dimmensional architecture for the attachment, growth and migration of rat BMMSCs and did not impair the expression of the stemness genes. We then investigated the effect of collagen/BM-MSCs constructs in the healing of severe uterine injury in rats (partial full thickness uterine excision). At four weeks after the transplantation of collagen/BM-MSCs constructs, BM-MSCs were mainly located to the basal membrane of regenerative endometrium. The wounded tissue adjacent to collagen/BM-MSCs constructs expressed higher level of bFGF, IGF-1, TGF beta 1 and VEGF than the corresponding tissue in rats receiving collagen construct alone or in spontaneous regeneration group. Moreover, the collagen/BM-MSCs system increased proliferative abilities of uterine endometrial and muscular cells, facilitated microvasculature regeneration, and restored the ability of endometrium to receive the embryo and support its development to a viable stage. Our findings indicate that BM-MSCs may support uterine tissue regeneration. (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4888 / 4900
页数:13
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