Krause Matthew P, Liu Ying, Vu Vivian, Chan Lawrence, Xu Aimin, Riddell Michael C, Sweeney Gary, Hawke Thomas J
School of Kinesiology and Health Science, York University, Toronto, Ontario, Canada.
Am J Physiol Cell Physiol. 2008 Jul;295(1):C203-12. doi: 10.1152/ajpcell.00030.2008. Epub 2008 May 7.
Adiponectin (Ad) is linked to various disease states and mediates antidiabetic and anti-inflammatory effects. While it was originally thought that Ad expression was limited to adipocytes, we demonstrate here that Ad is expressed in mouse skeletal muscles and within differentiated L6 myotubes, as assessed by RT-PCR, Western blot, and immunohistochemical analyses. Serial muscle sections stained for fiber type, lipid content, and Ad revealed that muscle fibers with elevated intramyocellular Ad expression were consistently type IIA and IID fibers with detectably higher intramyocellular lipid (IMCL) content. To determine the effect of Ad on muscle phenotype and function, we used an Ad-null [knockout (KO)] mouse model. Body mass increased significantly in 24-wk-old KO mice [+5.5 +/- 3% relative to wild-type mice (WT)], with no change in muscle mass observed. IMCL content was significantly increased (+75.1 +/- 25%), whereas epididymal fat mass, although elevated, was not different in the KO mice compared with WT (+35.1 +/- 23%; P = 0.16). Fiber-type composition was unaltered, although type IIB fiber area was increased in KO mice (+25.5 +/- 6%). In situ muscle stimulation revealed lower peak tetanic forces in KO mice relative to WT (-47.5 +/- 6%), with no change in low-frequency fatigue rates. These data demonstrate that the absence of Ad expression causes contractile dysfunction and phenotypical changes in skeletal muscle. Furthermore, we demonstrate that Ad is expressed in skeletal muscle and that its intramyocellular localization is associated with elevated IMCL, particularly in type IIA/D fibers.
脂联素(Ad)与多种疾病状态相关,并介导抗糖尿病和抗炎作用。虽然最初认为Ad的表达仅限于脂肪细胞,但我们在此证明,通过逆转录聚合酶链反应(RT-PCR)、蛋白质印迹法和免疫组织化学分析评估,Ad在小鼠骨骼肌和分化的L6肌管中表达。对纤维类型、脂质含量和Ad进行染色的连续肌肉切片显示,细胞内Ad表达升高的肌纤维始终是IIA型和IID型纤维,其细胞内脂质(IMCL)含量明显更高。为了确定Ad对肌肉表型和功能的影响,我们使用了Ad基因敲除(KO)小鼠模型。24周龄的KO小鼠体重显著增加[相对于野生型小鼠(WT)增加了5.5±3%],而肌肉质量没有变化。IMCL含量显著增加(+75.1±25%),而附睾脂肪量虽然有所升高,但与WT相比,KO小鼠没有差异(+35.1±23%;P = 0.16)。纤维类型组成未改变,尽管KO小鼠的IIB型纤维面积增加(+25.5±6%)。原位肌肉刺激显示,与WT相比,KO小鼠的强直收缩峰值力较低(-47.5±6%),低频疲劳率没有变化。这些数据表明,Ad表达缺失会导致骨骼肌收缩功能障碍和表型变化。此外,我们证明Ad在骨骼肌中表达,其细胞内定位与IMCL升高有关,特别是在IIA/D型纤维中。