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The Unique Mitochondrial Form and Function of Antarctic Channichthyid Icefishes

机译:南极Channichthyid冰鱼的独特线粒体形式和功能

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Antarctic icefishes of the family Channichthyidae are the only vertebrate animals that as adults do not express the circulating oxygen-binding protein hemoglobin (Hb). Six of the 16 family members also lack the intracellular oxygen-binding protein myoglobin (Mb) in the ventricle of their hearts and all lack Mb in oxidative skeletal muscle. The loss of Hb has led to substantial remodeling in the cardiovascular system of icefishes to facilitate adequate oxygenation of tissues. One of the more curious adaptations to the loss of Hb and Mb is an increase in mitochondrial density in cardiac myocytes and oxidative skeletal muscle fibers. The proliferation of mitochondria in the aerobic musculature of icefishes does not arise through a canonical pathway of mitochondrial biogenesis. Rather, the biosynthesis of mitochondrial phospholipids is up-regulated independently of the synthesis of proteins and mitochondrial DNA, and newly-synthesized phospholipids are targeted primarily to the outer-mitochondrial membrane. Consequently, icefish mitochondria have a higher lipid-to-protein ratio compared to those from red-blooded species. Elevated levels of nitric oxide in the blood plasma of icefishes, compared to red-blooded notothenioids, may mediate alterations in mitochondrial density and architecture. Modifications in mitochondrial structure minimally impact state III respiration rates but may significantly enhance intracellular diffusion of oxygen. The rate of oxygen diffusion is greater within the hydrocarbon core of membrane lipids compared to the aqueous cytosol and impeded only by proteins within the lipid bilayer. Thus, the proliferation of icefish’s mitochondrial membranes provides an optimal conduit for the intracellular diffusion of oxygen and compensates for the loss of Hb and Mb. Currently little is known about how mitochondrial phospholipid synthesis is regulated and integrated into mitochondrial biogenesis. The unique architecture of the oxidative muscle cells of icefishes highlights the need for further studies in this area.
机译:象鼻鱼类科的南极冰鱼是仅有的成年后不表达循环氧结合蛋白血红蛋白(Hb)的脊椎动物。 16个家庭成员中有6个在其心室中还缺乏细胞内氧结合蛋白肌红蛋白(Mb),并且在氧化性骨骼肌中都缺乏Mb。 Hb的损失导致了冰鱼心血管系统的实质性重塑,以促进组织的充分充氧。对Hb和Mb丢失的更奇怪的适应之一是心肌细胞和氧化性骨骼肌纤维中线粒体密度的增加。线粒体在有氧鱼类的肌肉组织中的增殖不是通过线粒体生物发生的经典途径产生的。而是,线粒体磷脂的生物合成独立于蛋白质和线粒体DNA的合成而被上调,并且新合成的磷脂主要靶向线粒体外膜。因此,与红血种相比,冰鱼线粒体的脂蛋白比率更高。与红血型类胡萝卜素相比,冰鱼血浆中一氧化氮水平的升高可能介导线粒体密度和结构的改变。线粒体结构的改变最小程度地影响状态III的呼吸速率,但可能会显着增强细胞内氧气的扩散。与水性细胞溶胶相比,膜脂质的烃核内的氧扩散速率更大,并且仅受脂质双层中的蛋白质阻碍。因此,冰鱼线粒体膜的增殖为氧气在细胞内的扩散提供了最佳管道,并补偿了Hb和Mb的损失。目前关于线粒体磷脂合成如何被调节并整合到线粒体生物发生中的了解甚少。冰鱼的氧化肌细胞的独特结构突显了对该领域进一步研究的需要。

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