Yang Sheng, Laumonier Thomas, Menetrey Jacques
Department of Orthopedic Surgery, Affiliated Zhongshan Hospital of Dalian University, Dalian 116001, China.
Sci China C Life Sci. 2007 Aug;50(4):438-46. doi: 10.1007/s11427-007-0065-6.
Myoblast transplantation (MT) is a cell-based gene therapy treatment, representing a potential treatment for Duchenne muscular dystrophy (DMD), cardiac failure and muscle trauma. The rapid and massive death of transplanted cells after MT is considered as a major hurdle which limits the efficacy of MT treatment. Heat shock proteins (HSPs) are overexpressed when cells undergo various insults. HSPs have been described to protect cells in vivo and in vitro against diverse insults. The aim of our study is to investigate whether HSP overexpression could increase myoblast survival after autotransplantation in pig intact skeletal muscle. HSP expression was induced by warming the cells at 42 degrees C for 1 h. HSP70 expression was quantified by Western blot and flow cytometry 24 h after the treatment. To investigate the myogenic characteristics of myoblasts, desmin and CD56 were analysed by Western blot and flow cytometry; and the fusion index was measured. We also quantified cell survival after autologous transplantation in pig intact skeletal muscle and followed cell integration. Results showed that heat shock treatment of myoblasts induced a significative overexpression of the HSP70 (P < 0.01) without loss of their myogenic characteristics as assessed by FACS and fusion index. In vivo (n=7), the myoblast survival rate was not significantly different at 24 h between heat shock treated and nontreated cells (67.69% +/- 8.35% versus 58.79% +/- 8.35%, P > 0.05). However, the myoblast survival rate in the heat shocked cells increased by twofold at 48 h (53.32% +/- 8.22% versus 28.27% +/- 6.32%, P < 0.01) and more than threefold at 120 h (26.33% +/- 5.54% versus 8.79% +/- 2.51%, P < 0.01). Histological analysis showed the presence of non-heat shocked and heat shocked donor myoblasts fused with host myoblasts. These results suggested that heat shock pretreatment increased the HSP70 expression in porcine myoblasts, and improved the survival rate after autologous transplantation. Therefore, heat shock pretreatment of myoblast in vitro is a simple and effective way to enhance cell survival after transplantation in pig. It might represent a potential method to overcome the limitations of MT treatment.
成肌细胞移植(MT)是一种基于细胞的基因治疗方法,是杜氏肌营养不良症(DMD)、心力衰竭和肌肉创伤的潜在治疗手段。MT后移植细胞的快速大量死亡被认为是限制MT治疗效果的主要障碍。当细胞受到各种损伤时,热休克蛋白(HSPs)会过度表达。已有研究表明,HSPs在体内和体外均可保护细胞免受多种损伤。本研究的目的是探讨HSP过度表达是否能提高猪完整骨骼肌自体移植后成肌细胞的存活率。通过将细胞在42℃加热1小时来诱导HSP表达。处理24小时后,通过蛋白质免疫印迹法和流式细胞术对HSP70表达进行定量分析。为了研究成肌细胞的成肌特性,通过蛋白质免疫印迹法和流式细胞术分析结蛋白和CD56;并测量融合指数。我们还对猪完整骨骼肌自体移植后的细胞存活率进行了定量分析,并跟踪细胞整合情况。结果显示,对成肌细胞进行热休克处理可诱导HSP70显著过度表达(P < 0.01),且通过流式细胞术和融合指数评估,其成肌特性并未丧失。在体内实验(n = 7)中,热休克处理组和未处理组细胞在24小时时的成肌细胞存活率无显著差异(67.69% ± 8.35%对58.79% ± 8.35%,P > 0.05)。然而,热休克处理组细胞在48小时时的成肌细胞存活率增加了两倍(53.32% ± 8.22%对28.27% ± 6.32%,P < 0.01),在120小时时增加了三倍多(26.33% ± 5.54%对8.79% ± 2.51%,P < 0.01)。组织学分析显示存在未热休克和热休克的供体成肌细胞与宿主成肌细胞融合。这些结果表明,热休克预处理可增加猪成肌细胞中HSP70的表达,并提高自体移植后的存活率。因此,体外对成肌细胞进行热休克预处理是提高猪移植后细胞存活率的一种简单有效的方法。它可能是克服MT治疗局限性的一种潜在方法。