César Matthieu, Roussanne-Domergue Sophie, Coulet Bertrand, Gay Stéphanie, Micallef Jean-Paul, Chammas Michel, Reyne Yves, Bacou Francis
Institut National de la Recherche Agronomique, UMR 866 Différenciation Cellulaire et Croissance, 2 Place Pierre Viala, F-34060 Montpellier, France.
Muscle Nerve. 2008 Feb;37(2):219-30. doi: 10.1002/mus.20918.
We previously showed that transfer of adult myoblasts (MB) into cardiotoxin-damaged muscle improved the properties of reinnervated tibialis anterior muscle of rabbits. However, this cell therapy protocol cannot be applied to humans because of the hazardous effects of the myotoxin. To circumvent this approach, we used the recently developed high-density injection technique to autotransplant cultured cells 1 mm from each other into the tibialis anterior muscle without previous cardiotoxin-induced damage. Two months after transection and immediate suture of the common peroneal nerve, we transferred by this technique two types of precursor cells, MB or cells isolated from the adipose tissue stromal vascular fraction. In contrast to our previous results, muscles studied at 4 months showed no benefits in terms of function or morphology, whatever the transferred cells. These results, together with the results of earlier studies, emphasize the importance of delivery methods and the muscle environment in supporting cell integration into host tissues.
我们之前表明,将成年成肌细胞(MB)移植到心脏毒素损伤的肌肉中可改善家兔再支配的胫前肌的性能。然而,由于肌毒素的有害作用,这种细胞治疗方案无法应用于人类。为了规避这种方法,我们使用了最近开发的高密度注射技术,将彼此相距1毫米的培养细胞自体移植到胫前肌中,而无需事先进行心脏毒素诱导的损伤。在腓总神经横断并立即缝合两个月后,我们通过这种技术移植了两种类型的前体细胞,即MB或从脂肪组织基质血管成分中分离的细胞。与我们之前的结果相反,无论移植何种细胞,在4个月时研究的肌肉在功能或形态方面均未显示出益处。这些结果与早期研究的结果一起,强调了递送方法和肌肉环境在支持细胞整合到宿主组织中的重要性。