4.8 Article

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

期刊

BIOMATERIALS
卷 35, 期 18, 页码 4888-4900

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2014.02.046

关键词

Uterine regeneration; Collagen scaffold; Bone marrow-derived mesenchymal stem; cells; Microvasculature

资金

  1. Ministry of Science and Technology of China [2010CB945104, 2007CB948004]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA01030401]
  3. Maternal-Fetal Medicine from Jiangsu Province Health Department of China
  4. Key Laboratory of Obstetric & Gynecologic Diseases, National Ministry of Health and Nanjing Health Department
  5. MRC [G1000816] Funding Source: UKRI
  6. Medical Research Council [G1000816] Funding Source: researchfish

向作者/读者索取更多资源

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.

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