Haigh Sarah E, Twig Gilad, Molina Anthony A J, Wikstrom Jakob D, Deutsch Motti, Shirihai Orian S
Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, 136 Harrison Ave, Boston, MA 02111, USA.
Novartis Found Symp. 2007;287:21-36; discussion 36-46. doi: 10.1002/9780470725207.ch3.
Mitochondrial connectivity is characterized by matrix lumen continuity and by dynamic rewiring through fusion and fission events. While these mechanisms homogenize the mitochondrial population, a number of studies looking at mitochondrial membrane potential have demonstrated that mitochondria exist as a heterogeneous population within individual cells. To address the relationship between mitochondrial dynamics and heterogeneity, we tagged and tracked individual mitochondria over time while monitoring their mitochondrial membrane potential (deltapsi(m)). By utilizing photoactivatible-GFP (PA-GFP), targeted to the mitochondrial matrix, we determined the boundaries of the individual mitochondrion. A single mitochondrion is defined by the continuity of its matrix lumen. The boundaries set by luminal continuity matched those set by electrical coupling, indicating that the individual mitochondrion is equipotential throughout the entire organelle. Similar results were obtained with PA-GFP targeted to the inner membrane indicating that matrix continuity parallels inner membrane continuity. Sequential photoconversion of matrix PA-GFP in multiple locations within the mitochondrial web reveals that each ramified mitochondrial structure is composed of juxtaposed but discontinuous units. Moreover, as many as half of the events in which mitochondria come into contact, do not result in fusion. While all fission events generated two electrically uncoupled discontinuous matrices, the two daughter mitochondria frequently remained juxtaposed, keeping the tubular appearance unchanged. These morphologically invisible fission events illustrate the difference between mitochondrial fission and fragmentation; the latter representing the movement and separation of disconnected units. Simultaneous monitoring of deltapsi(m) of up to four individual mitochondria within the same cell revealed that subcellular heterogeneity in deltapsi(m) does not represent multiple unstable mitochondria that appear 'heterogeneous' at any given point, but rather multiple stable, but heterogeneous units.
线粒体连接性的特征在于基质腔的连续性以及通过融合和裂变事件进行的动态重塑。虽然这些机制使线粒体群体同质化,但一些关于线粒体膜电位的研究表明,线粒体在单个细胞内以异质群体的形式存在。为了研究线粒体动态性与异质性之间的关系,我们在监测单个线粒体的线粒体膜电位(Δψm)的同时,对其进行标记并随时间追踪。通过利用靶向线粒体基质的光激活绿色荧光蛋白(PA-GFP),我们确定了单个线粒体的边界。单个线粒体由其基质腔的连续性定义。由腔连续性设定的边界与由电偶联设定的边界相匹配,这表明单个线粒体在整个细胞器中是等电位的。将PA-GFP靶向内膜也获得了类似的结果,表明基质连续性与内膜连续性平行。对线粒体网络内多个位置的基质PA-GFP进行连续光转化,结果显示每个分支状的线粒体结构都由并列但不连续的单元组成。此外,线粒体发生接触的事件中,多达一半不会导致融合。虽然所有裂变事件都会产生两个电不偶联的不连续基质,但两个子线粒体经常保持并列,管状外观不变。这些形态上不可见的裂变事件说明了线粒体裂变和碎片化之间的区别;后者代表不相连单元的移动和分离。同时监测同一细胞内多达四个单个线粒体的Δψm,结果显示Δψm的亚细胞异质性并不代表在任何给定时刻看似“异质”的多个不稳定线粒体,而是代表多个稳定但异质的单元。