Carvajal Monroy P L, Grefte S, Kuijpers-Jagtman A M, Von den Hoff J W, Wagener F A D T G
1 Department of Orthodontics and Craniofacial Biology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands.
2 Human and Animal Physiology, Wageningen University, Wageningen, The Netherlands.
J Dent Res. 2017 Mar;96(3):331-338. doi: 10.1177/0022034516679136. Epub 2016 Nov 19.
Although palatal muscle reconstruction in patients with cleft palate takes place during early childhood, normal speech development is often not achieved. We hypothesized that the intrinsic properties of head satellite cells (SCs) and the young age of these patients contribute to the poor muscle regeneration after surgery. First, we studied the fiber type distribution and the expression of SC markers in ex vivo muscle tissue from head (branchiomeric) and limb (somite-derived) muscles from neonatal (2-wk-old) and young (9-wk-old) rats. Next, we cultured SCs isolated from these muscles for 5, 7, and 9 d, and investigated the in vitro expression of SC markers, as well as changes in proliferation, early differentiation, and fusion index (myotube formation) in these cells. In our ex vivo samples, we found that virtually all myofibers in both the masseter (Mass) and the levator veli palatini (LVP) muscles contained fast myosin heavy chain (MyHC), and a small percentage of digastric (Dig) and extensor digitorum longus myofibers also contained slow MyHC. This was independent of age. More SCs were found in muscles from neonatal rats as compared with young rats [17.6 (3.8%) v. 2.3 (1.6%); P < 0.0001]. In vitro, young branchiomeric head muscle (BrHM) SCs proliferated longer and differentiated later than limb muscle SCs. No differences were found between SC cultures from the different BrHMs. SC cultures from neonatal muscles showed a much higher proliferation index than those from young animals at 5 d (0.8 v. 0.2; P < 0.001). In contrast, the fusion index in neonate SCs was about twice as low as that in SCs from young muscles at 9 d [27.6 (1.4) v. 62.8 (10.2), P < 0.0001]. In conclusion, SCs from BrHM differ from limb muscles especially in their delayed differentiation. SCs from neonatal muscles form myotubes less efficiently than those from young muscles. These age-dependent differences in stem cell properties urge careful consideration for future clinical applications in patients with cleft palate.
尽管腭裂患者的腭肌重建在幼儿期进行,但通常无法实现正常的言语发育。我们推测,头部卫星细胞(SCs)的内在特性以及这些患者的幼年时期导致了术后肌肉再生不良。首先,我们研究了新生(2周龄)和幼年(9周龄)大鼠头部(鳃弓衍生)和肢体(体节衍生)肌肉的离体肌肉组织中的纤维类型分布和SCs标志物的表达。接下来,我们将从这些肌肉中分离出的SCs培养5、7和9天,并研究这些细胞中SCs标志物的体外表达以及增殖、早期分化和融合指数(肌管形成)的变化。在我们的离体样本中,我们发现咬肌(Mass)和腭帆提肌(LVP)中的几乎所有肌纤维都含有快肌球蛋白重链(MyHC),并且一小部分二腹肌(Dig)和趾长伸肌肌纤维也含有慢MyHC。这与年龄无关。与幼年大鼠相比,新生大鼠肌肉中发现了更多的SCs[17.6(3.8%)对2.3(1.6%);P<0.0001]。在体外,幼年鳃弓头部肌肉(BrHM)SCs的增殖时间更长,分化时间比肢体肌肉SCs更晚。不同BrHMs的SCs培养物之间未发现差异。新生肌肉的SCs培养物在5天时的增殖指数比幼年动物的培养物高得多(0.8对0.2;P<0.001)。相比之下,新生SCs的融合指数在9天时约为幼年肌肉SCs融合指数的一半[27.6(1.4)对62.8(10.2),P<0.0001]。总之,BrHM的SCs与肢体肌肉不同,尤其是在它们延迟分化方面。新生肌肉的SCs形成肌管的效率低于幼年肌肉的SCs。干细胞特性的这些年龄依赖性差异促使在腭裂患者未来临床应用中仔细考虑。