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Epidermal growth factor can optimize a serum-free culture system for bone marrow stem cell proliferation in a miniature pig model
Authors:Xuan Wang  Feng Zheng  Ousheng Liu  Shutao Zheng  Yishan Liu  Yuehong Wang  Zhangui Tang  Liangjun Zhong
Institution:1. Department of Oral and Maxillofacial Surgery, Xiangya Hospital, Central South University, No. 110 Xiangya Road, Changsha, Hunan, 410078, China
2. Department of Pediatric Dentistry and Oral Prevention and Health Care, 1st Affiliated Hospital Xinjiang Medical University, No. 1, Liyushan South Road, Urumqi, Xinjiang Uygur Autonomous Region, 830011, China
3. Department of Cardiovascular Surgery, 1st Affiliated Hospital of Xinjiang Medical University, No. 1, Liyushan South Road, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China
4. Clinical Medical Research Institute, State Key Lab Incubation Base of Xinjiang Major Diseases Research, First Affiliated Hospital of Xinjiang Medical University, No. 1, Liyushan South Road, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China
5. Department of Dental, Affiliated Hospital of Hangzhou Normal University, No. 126, Wenzhou Road, Gong-shu District, Hangzhou, Zhejiang, 310011, China
Abstract:Bone marrow-derived mesenchymal stem cells have become an attractive cell source for periodontal ligament regeneration treatment because of their potential to engraft to several tissue types after injury. Most researchers have focused on the transplantation process, but few have paid attention to cell safety concerns and rapid proliferation before transplantation. Using serum-free medium to culture stem cells may be an effective method to avoid problems associated with exogenous serum and the addition of growth factors to promote cell proliferation. Here, we randomly divided our serum-free cultures and treated them with different levels of epidermal growth factor (EGF). We then evaluated changes in rates of cell adhesion, proliferation, apoptosis, and cell cycle ratio as well as their differentiation potential. The data showed that all of these parameters were significantly different when comparing serum-free cultures with and without 10 nM/L EGF (p?<?0.05/0.01); however, cells with 10 nM/L EGF did not respond differently than cells grown in standard serum-containing media without EGF (p?>?0.05). In summary, our results demonstrate that 10 nM/L EGF was the optimal dose for serum-free culture, which can replace traditional standard serum medium for in vitro expansion of miniature pig bone marrow-derived mesenchymal stem cells.
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