Kadaja Lumme, Kisand Kai E, Peet Nadezhda, Braun Urmo, Metsküla Kaja, Teesalu Kaupo, Vibo Riina, Kisand Kalle V, Uibo Raivo, Jockusch Harald, Seppet Enn K
Department of Pathophysiology, Faculty of Medicine, University of Tartu, Tartu, Estonia.
Mol Cell Biochem. 2004 Jan-Feb;256-257(1-2):291-303. doi: 10.1023/b:mcbi.0000009876.23921.e6.
The effect of IgG purified from the sera of healthy persons and patients with primary biliary cirrhosis (PBC) and chronic hepatitis (CH) on ADP dependent respiration (oxidative phosphorylation) in skinned muscle fibers from rat oxidative muscles (heart and M. soleus) and glycolytic skeletal muscle (M. gastrocnemius) was studied. The results show that IgG from three different sources inhibited the rate of respiration by 13, 44 and 42%, respectively, these effects being equally expressed in both types of oxidative muscles, whereas no inhibition was observed in glycolytic muscle. The following washout of unbound IgG did not abolish the inhibition of respiration suggesting that the specific interaction of IgG with antigens had taken place. Laser confocal analysis revealed binding of IgG predominantly to the sarcomeric structures such as Z-disk and M-lines in the cardiomyocytes. The staining of IgG within Z-disks and intermitochondrial space coincided throughout the muscle cells so that transversally serial spaces, each containing mitochondria and adjacent sarcomere, became clearly visible. When the IgG from a CH patient was incubated with the skinned myocardial fibers of the desmin knockout mice, its binding to Z-disks and the sarcomeric area was found to be similar to that in normal cardiac muscle. However, the transversal staining pattern was disintegrated, because of the slippage of the myofibrils in relation to each other and accumulation of mitochondria between them. These observations support the recent hypothesis that in oxidative muscles the mitochondria and adjacent sarcomeres form complexes, termed as the intracellular energetic units, ICEUs. Moreover, they indicate that human autoantibodies can be useful tools for localizing the proteins responsible for formation of ICEUs and modulation of their function. Thus, it appears that the proteins associated with the Z-disks and M-lines may participate in formation of ICEUs and that binding of IgG to these proteins decreases the access of exogenous adenine nucleotides to mitochondria, which manifests as decreased rate of ADP-dependent respiration.
研究了从健康人、原发性胆汁性肝硬化(PBC)患者和慢性肝炎(CH)患者血清中纯化的IgG对大鼠氧化型肌肉(心脏和比目鱼肌)和糖酵解型骨骼肌(腓肠肌)的脱膜肌纤维中ADP依赖性呼吸(氧化磷酸化)的影响。结果表明,来自三种不同来源的IgG分别抑制呼吸速率13%、44%和42%,这些作用在两种氧化型肌肉中均有同等程度的表现,而在糖酵解型肌肉中未观察到抑制作用。随后洗脱未结合的IgG并未消除对呼吸的抑制作用,这表明IgG与抗原发生了特异性相互作用。激光共聚焦分析显示,IgG主要与心肌细胞中的肌节结构如Z盘和M线结合。Z盘和线粒体间空间内的IgG染色在整个肌肉细胞中是一致的,从而使每个包含线粒体和相邻肌节的横向连续空间清晰可见。当将CH患者的IgG与结蛋白基因敲除小鼠的脱膜心肌纤维一起孵育时,发现其与Z盘和肌节区域的结合与正常心肌中的情况相似。然而,由于肌原纤维彼此之间的滑动以及它们之间线粒体的积累,横向染色模式被破坏。这些观察结果支持了最近的假说,即在氧化型肌肉中,线粒体和相邻的肌节形成复合物,称为细胞内能量单位(ICEUs)。此外,它们表明人类自身抗体可能是定位负责ICEUs形成及其功能调节的蛋白质的有用工具。因此,似乎与Z盘和M线相关的蛋白质可能参与ICEUs的形成,并且IgG与这些蛋白质的结合减少了外源性腺嘌呤核苷酸进入线粒体的机会,这表现为ADP依赖性呼吸速率降低。