| Literature DB >> 28486025 |
Chenchen Feng1, Xuan Luo1, Na He1, Huitang Xia2,3, Xiaoteng Lv1, Xue Zhang2,3, Dan Li2,3, Fei Wang1, Jiaping He1, Li Zhang1, Xiangming Lin4, Liping Lin4, Huabin Yin4, Jiyin He5, Jingwu Wang6, Wei Cao1, Richard Wang1, Guangdong Zhou2,3,7, Wen Wang1.
Abstract
Although a number of studies have reported efficacy of autologous adipose-derived mesenchymal stem cells (AD-MSCs) in treating osteoarthritis (OA) no reliable evidences demonstrate whether allogeneic AD-MSCs can efficiently block OA progression in a large animal model. This study explored the efficacy and survival of allogeneic AD-MSCs combined with hyaluronic acid (HA) after intra-articular (IA) injection in a sheep OA model, which were conventionally established by anterior cruciate ligament resection and medial meniscectomy. Allogeneic AD-MSCs from donor sheep at high (5 × 107 cells) and low (1 × 107 cells) doses combined with HA, HA alone, or saline alone were injected into the OA sheep at 3 and 6 weeks after surgery, respectively. Evaluations by magnetic resonance imaging (MRI), macroscopy, micro-computed tomography, and cartilage-specific staining demonstrated that AD-MSCs+HA treated groups preserved typical articular cartilage feature. Inflammatory factors from synovial fluid of AD-MSCs+HA treated groups were significantly lower than those in the HA alone group. Notably, transforming growth factor beta 1 and insulin-like growth factor 1 were detected in the supernatant of cultured AD-MSCs. In addition, labeling signals of allogeneic AD-MSCs could be detected by MRI after 14 weeks of injection and be found in synovium by histology. These results indicated that IA injection of allogeneic AD-MSCs combined with HA could efficiently block OA progression and promote cartilage regeneration and allogeneic AD-MSCs might survive at least 14 weeks after IA injection.Entities:
Keywords: adipose-derived mesenchymal stem cells; allogeneic; cell tracking; hyaluronic acid; intra-articular injection; osteoarthritis; sheep model; superparamagnetic iron oxide
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Year: 2017 PMID: 28486025 DOI: 10.1089/ten.TEA.2017.0039
Source DB: PubMed Journal: Tissue Eng Part A ISSN: 1937-3341 Impact factor: 3.845