Bruusgaard J C, Liestøl K, Gundersen K
Department of Molecular Biosciences, University of Oslo, PO Box 1041, Blindern NO-0316, Oslo, Norway.
J Appl Physiol (1985). 2006 Jun;100(6):2024-30. doi: 10.1152/japplphysiol.00913.2005. Epub 2006 Feb 23.
We have recently published a new technique for visualizing nuclei in living muscle fibers of intact animals, based on microinjection of labeled DNA into single myofibers, excluding satellite cells (Bruusgaard JC, Liestol K, Ekmark M, Kollstad K, and Gundersen K. J Physiol 551: 467-478, 2003). In the present study, we use this technique to study fiber segments of soleus and extensor digitorum longus (EDL) muscles from mice aged 2, 14, and 23 mo. As the animals maturing from 2 to 14 mo, they displayed an increase in size and number of nuclei. Soleus showed little change in nuclear domain size, whereas this increased by 88% in the EDL. For 14-mo-old animals, no significant correlation between fiber size and nuclear number was observed (R2=0.18, P=0.51) despite a fourfold variation in cytoplasmic volume. This suggests that size and nuclear number is uncoupled in middle-aged mice. When animals aged from 14 to 23 mo, EDL IIb, but not soleus, fibers atrophied by 41%. Both EDL and soleus displayed a reduction in number of nuclei: 20 and 16%, respectively. A positive correlation between number of nuclei and size was observed at 2 mo, and this reappeared in old mice. The atrophy in IIb fibers at old age was accompanied by a disturbance in the orderly positioning of nuclei that is so prominent in glycolytic fibers at younger age. In old animals, changes in nuclear shape and in the peri- and internuclear microtubule network were also observed. Thus changes in myonuclear number and distribution, perhaps related to alterations in the microtubular network, may underlie some of the adverse consequences of aging on skeletal muscle size and function.
我们最近发表了一种可视化完整动物活体肌纤维中细胞核的新技术,该技术基于将标记的DNA显微注射到单个肌纤维中,不包括卫星细胞(Bruusgaard JC、Liestol K、Ekmark M、Kollstad K和Gundersen K.《生理学杂志》551: 467 - 478, 2003)。在本研究中,我们使用该技术研究2、14和23月龄小鼠的比目鱼肌和趾长伸肌(EDL)的纤维段。随着动物从2月龄发育到14月龄,它们的细胞核大小和数量增加。比目鱼肌的核域大小变化不大,而EDL中的核域大小增加了88%。对于14月龄的动物,尽管细胞质体积有四倍的变化,但未观察到纤维大小与核数量之间存在显著相关性(R2 = 0.18,P = 0.51)。这表明中年小鼠的大小和核数量是不相关的。当动物从14月龄到23月龄时,EDL的IIb型纤维(比目鱼肌未出现)萎缩了41%。EDL和比目鱼肌的细胞核数量均减少,分别减少了20%和16%。在2月龄时观察到细胞核数量与大小之间呈正相关,这种相关性在老年小鼠中再次出现。老年时IIb型纤维的萎缩伴随着细胞核有序定位的紊乱,而这种定位在年轻的糖酵解纤维中非常明显。在老年动物中,还观察到细胞核形状以及核周和核内微管网络的变化。因此,肌核数量和分布的变化,可能与微管网络的改变有关,可能是衰老对骨骼肌大小和功能产生一些不良后果的基础。