Institute of Anatomy, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Anat Rec (Hoboken). 2012 Aug;295(8):1364-72. doi: 10.1002/ar.22512. Epub 2012 Jun 18.
In contrast to limb muscles where neonatal myosin (MyHC-neo) is present only shortly after birth, adult masseter muscles contain a substantial portion of MyHC-neo, which is coexpressed with mature MyHC isoforms. Changes in the numerical and area proportion of muscle fibers containing MyHC-neo in masseter muscle with aging could be expected, based on previously reported findings that (i) developmental MyHC-containing muscle fibers exhibit lower shortening velocities compared to fibers with exclusively fast MyHC isoforms and (ii) transformation toward faster phenotype occurs in elderly compared to young masseter muscle. In this study, we detected MyHC isoforms in the anterior superficial part of the human masseter muscle in a sufficiently large sample of young, middle-aged, and elderly subjects to reveal age-related changes in the coexpression of MyHC-neo with adult MyHC isoforms. MyHC isoforms were visualized with immunoperoxidase method and the results were presented by (i) the area proportion of fibers containing particular MyHC isoforms and (ii) the numerical proportion of fiber types defined by MyHC-1, -2a, -2x, and -neonatal isoform expression from a successive transverse sections. We found a lower numerical and area proportion of fibers expressing MyHC-neo as well as a lower area proportion of fibers containing MyHC-1 in elderly than in young subjects. We conclude that the diminished expression of MyHC-neo with age could point to a lower regeneration capacity of masseter muscle in the elderly.
与肢体肌肉不同,新生儿肌球蛋白(MyHC-neo)仅在出生后短暂存在,而成年咬肌含有相当一部分 MyHC-neo,它与成熟的 MyHC 同工型共同表达。基于之前的研究发现,随着年龄的增长,咬肌中含有 MyHC-neo 的肌纤维数量和面积比例可能会发生变化:(i)发育中的含有 MyHC 的肌纤维与仅含有快肌 MyHC 同工型的纤维相比,缩短速度较低;(ii)与年轻的咬肌相比,老年咬肌向更快的表型转化。在这项研究中,我们在足够大的年轻、中年和老年受试者的咬肌前浅层部分检测到了 MyHC 同工型,以揭示与年龄相关的 MyHC-neo 与成人 MyHC 同工型共同表达的变化。我们使用免疫过氧化物酶方法可视化了 MyHC 同工型,并通过以下方式呈现结果:(i)特定 MyHC 同工型所含纤维的面积比例;(ii)通过 MyHC-1、-2a、-2x 和 -neonatal 同工型表达的连续横切片定义的纤维类型的数量比例。我们发现,老年受试者的 MyHC-neo 表达的数量和面积比例较低,而含有 MyHC-1 的纤维面积比例也较低。我们得出结论,随着年龄的增长,MyHC-neo 的表达减少可能表明老年咬肌的再生能力较低。