Lynch G S, Rafael J A, Hinkle R T, Cole N M, Chamberlain J S, Faulkner J A
Institute of Gerontology, University of Michigan, Ann Arbor 48109-2007, USA.
Am J Physiol. 1997 Jun;272(6 Pt 1):C2063-8. doi: 10.1152/ajpcell.1997.272.6.C2063.
Diaphragm muscles of young (4- to 6-mo-old) mdx mice show severe fiber necrosis and have normalized forces and powers 60 and 46% of the values for control C57BL/10 mice. In contrast, microinjection of mdx mouse embryos with a truncated dystrophin minigene has produced young transgenic mdx (tg-mdx) mice with a level of dystrophin expression and structural and functional properties of diaphragm muscle strips measured in vitro not different from those of control mice. Whether dystrophin expression and functional corrections persist for the life span of these animals is not know. We tested the null hypothesis that, in old (24 mo) tg-mdx mice, dystrophin expression is adequate and diaphragm muscle strips have forces and powers not different from values for diaphragm muscle strips from young tg-mdx mice or control mice. Compared with control values, diaphragm muscle strips from old mdx mice had normalized forces and powers of 48 and 31%, respectively. Expression of dystrophin persisted in diaphragm muscles of old tg-mdx mice, and functional properties were not different from diaphragm muscles of young tg-mdx or young or old control mice. These results suggest that, with a transgenic animal approach, dystrophin expression and functional corrections persist for the life span of the animals.
年轻(4至6月龄)mdx小鼠的膈肌显示出严重的纤维坏死,其标准化后的力和功率分别为对照C57BL/10小鼠的60%和46%。相比之下,用截短的肌营养不良蛋白微型基因对mdx小鼠胚胎进行显微注射,产生了年轻的转基因mdx(tg-mdx)小鼠,其肌营养不良蛋白表达水平以及体外测量的膈肌条带的结构和功能特性与对照小鼠无异。尚不清楚这些动物一生中肌营养不良蛋白的表达和功能校正是否持续存在。我们检验了一个零假设,即在老年(24月龄)tg-mdx小鼠中,肌营养不良蛋白表达充足,膈肌条带的力和功率与年轻tg-mdx小鼠或对照小鼠的膈肌条带的值无差异。与对照值相比,老年mdx小鼠的膈肌条带标准化后的力和功率分别为48%和31%。老年tg-mdx小鼠的膈肌中持续存在肌营养不良蛋白表达,其功能特性与年轻tg-mdx小鼠或年轻或老年对照小鼠的膈肌无差异。这些结果表明,通过转基因动物方法,肌营养不良蛋白的表达和功能校正会在动物的一生中持续存在。