Tatsumi Ryuichi, Liu Xiaosong, Pulido Antonio, Morales Mark, Sakata Tomowa, Dial Sharon, Hattori Akihito, Ikeuchi Yoshihide, Allen Ronald E
Dept. of Animal Science, Hokkaido University, Sapporo, Japan.
Am J Physiol Cell Physiol. 2006 Jun;290(6):C1487-94. doi: 10.1152/ajpcell.00513.2005.
In the present study, we examined the roles of hepatocyte growth factor (HGF) and nitric oxide (NO) in the activation of satellite cells in passively stretched rat skeletal muscle. A hindlimb suspension model was developed in which the vastus, adductor, and gracilis muscles were subjected to stretch for 1 h. Satellite cells were activated by stretch determined on the basis of 5-bromo-2'-deoxyuridine (BrdU) incorporation in vivo. Extracts from stretched muscles stimulated BrdU incorporation in freshly isolated control rat satellite cells in a concentration-dependent manner. Extracts from stretched muscles contained the active form of HGF, and the satellite cell-activating activity could be neutralized by incubation with anti-HGF antibody. The involvement of NO was investigated by administering nitro-L-arginine methyl ester (L-NAME) or the inactive enantiomer N(G)-nitro-D-arginine methyl ester HCl (D-NAME) before stretch treatment. In vivo activation of satellite cells in stretched muscle was not inhibited by D-NAME but was inhibited by L-NAME. The activity of stretched muscle extract was abolished by L-NAME treatment but could be restored by the addition of HGF, indicating that the extract was not inhibitory. Finally, NO synthase activity in stretched and unstretched muscles was assayed in muscle extracts immediately after 2-h stretch treatment and was found to be elevated in stretched muscle but not in stretched muscle from L-NAME-treated rats. The results of these experiments demonstrate that stretching muscle liberates HGF in a NO-dependent manner, which can activate satellite cells.
在本研究中,我们检测了肝细胞生长因子(HGF)和一氧化氮(NO)在被动拉伸的大鼠骨骼肌卫星细胞激活过程中的作用。建立了一个后肢悬吊模型,其中股直肌、内收肌和股薄肌被拉伸1小时。根据体内5-溴-2'-脱氧尿苷(BrdU)掺入情况确定卫星细胞被拉伸激活。拉伸肌肉的提取物以浓度依赖的方式刺激新鲜分离的对照大鼠卫星细胞中的BrdU掺入。拉伸肌肉的提取物含有活性形式的HGF,并且卫星细胞激活活性可通过与抗HGF抗体孵育而被中和。在拉伸处理前给予硝基-L-精氨酸甲酯(L-NAME)或无活性对映体N(G)-硝基-D-精氨酸甲酯盐酸盐(D-NAME)来研究NO的参与情况。D-NAME不抑制拉伸肌肉中卫星细胞的体内激活,但L-NAME可抑制。L-NAME处理可消除拉伸肌肉提取物的活性,但添加HGF可恢复其活性,表明该提取物无抑制作用。最后,在2小时拉伸处理后立即在肌肉提取物中检测拉伸和未拉伸肌肉中的NO合酶活性,发现拉伸肌肉中的活性升高,但L-NAME处理的大鼠的拉伸肌肉中未升高。这些实验结果表明,拉伸肌肉以NO依赖的方式释放HGF,HGF可激活卫星细胞。