Murray John W, Yin David, Wolkoff Allan W
Marion Bessin Liver Research Center, Division of Gastroenterology and Liver Diseases, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York, United States of America.
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York, United States of America.
PLoS One. 2017 Sep 18;12(9):e0184898. doi: 10.1371/journal.pone.0184898. eCollection 2017.
There are surprisingly few studies that describe how the composition of cell culture medium may affect the trafficking of organelles. Here we utilize time lapse multi-channel fluorescent imaging to show that short term exposure of Huh-7 cells to medium lacking potassium, sodium, or chloride strongly reduces but does not eliminate the characteristic back and forth and cell-traversing movement of fluorescent EGF (FL-EGF) containing organelles. We focused on potassium because of its relatively low abundance in media and serum and its energy requiring accumulation into cells. Upon exposure to potassium free medium, organelle motility declined steadily through 90 min and then persisted at a low level. Reduced motility was confirmed in 5 independent cell lines and for organelles of the endocytic pathway (FL-EGF and Lysotracker), autophagosomes (LC3-GFP), and mitochondria (TMRE). As has been previously established, potassium free medium also inhibited endocytosis. We expected that diminished cellular metabolism would precede loss of organelle motility. However, extracellular flux analysis showed near normal mitochondrial oxygen consumption and only a small decrease in extracellular acidification, the latter suggesting decreased glycolysis or proton efflux. Other energy dependent activities such as the accumulation of Lysotracker, TMRE, DiBAC4(3), and the exclusion of propidium iodide remained intact, as did the microtubule cytoskeleton. We took advantage of cell free in vitro motility assays and found that removal of potassium or sodium from the reconstituted cytosolic medium decreased the movement of endosomes on purified microtubules. The results indicate that although changes in proton homeostasis and cell energetics under solute depletion are not fully understood, potassium as well as sodium appear to be directly required by the motile machinery of organelles for optimal trafficking.
令人惊讶的是,很少有研究描述细胞培养基的成分如何影响细胞器的运输。在这里,我们利用延时多通道荧光成像技术表明,将Huh-7细胞短期暴露于缺乏钾、钠或氯的培养基中,会强烈减少但不会消除含有荧光表皮生长因子(FL-EGF)的细胞器的特征性来回穿梭和跨细胞运动。由于钾在培养基和血清中的含量相对较低,且需要能量才能积累到细胞中,我们将重点放在了钾上。暴露于无钾培养基后,细胞器的运动能力在90分钟内稳步下降,然后维持在较低水平。在5个独立的细胞系以及内吞途径(FL-EGF和溶酶体示踪剂)、自噬体(LC3-GFP)和线粒体(TMRE)的细胞器中均证实了运动能力的降低。如先前已确定的那样,无钾培养基也抑制内吞作用。我们预计细胞器运动能力丧失之前细胞代谢会减弱。然而,细胞外通量分析显示线粒体氧消耗接近正常,细胞外酸化仅略有下降,后者表明糖酵解或质子外流减少。其他能量依赖活动,如溶酶体示踪剂、TMRE、DiBAC4(3)的积累以及碘化丙啶的排斥,以及微管细胞骨架均保持完整。我们利用无细胞体外运动分析,发现从重组细胞溶质培养基中去除钾或钠会降低内体在纯化微管上的移动。结果表明,尽管溶质耗竭下质子稳态和细胞能量学的变化尚未完全了解,但细胞器的运动机制似乎直接需要钾和钠才能实现最佳运输。