Halcrow Peter, Khan Nabab, Datta Gaurav, Ohm Joyce E, Chen Xuesong, Geiger Jonathan D
Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota 58201.
Department of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, New York 14263.
Cancer Rep (Hoboken). 2019 Dec;2(6). doi: 10.1002/cnr2.1193. Epub 2019 Jun 2.
Glioblastoma multiforme (GBM) is a very aggressive form of brain cancer that carries with it a tragically poor prognosis. As with many other forms of cancer, the extracellular environment near GBM tumors is acidified and is relevant to the pathogenesis of GBM because decreased pH promotes tumor cell invasion, increases angiogenesis, decreases immune surveillance, and increases resistance to possible treatments. Recently, vacuolar ATPase (v-ATPase), a proton pump that helps maintain the acidic environment in endosomes and lysosomes (hereafter referred to endolysosomes) as well as proton gradients across the plasma membrane, was identified as a novel therapeutic target for GBM. However, information is lacking about cancer cell and tissue pH of endolysosomes, cytosol and extracellular fluid.
Here, we measured endolysosome, cytosolic, and extracellular pH in U87MG cells in the absence and presence of the v-ATPase inhibitor bafilomycin A1.
In vitro measurements of U87MG cells were conducted using LysoSensor dye and a Lysosome-RFP dye for lysosome pH, BCECF-AM for cytosolic pH, and a pH-sensitive microprobe for extracellular pH.
Bafilomycin A1 increased endolysosome pH from 5.28 to 5.57, decreased cytosolic pH from 7.01 to 6.46, and increased extracellular pH from 7.18 to 7.40.
Here, we report the ability to make pH measurements in U87MG glioblastoma cells and discuss these results in the context of GBM pathogenesis and possible treatment. This might be of some importance in understanding the pathogenesis of GBM because the highly regulated stores of hydrogen (H) ions in endolysosomes can influence cytosolic and extracellular pH as well as the distribution, numbers, and sizes of endolysosomes.
多形性胶质母细胞瘤(GBM)是一种侵袭性很强的脑癌,预后极差。与许多其他癌症形式一样,GBM肿瘤附近的细胞外环境会酸化,这与GBM的发病机制相关,因为pH值降低会促进肿瘤细胞侵袭、增加血管生成、降低免疫监视并增加对可能治疗的抗性。最近,液泡ATP酶(v-ATP酶),一种有助于维持内体和溶酶体(以下简称内溶酶体)酸性环境以及跨质膜质子梯度的质子泵,被确定为GBM的新型治疗靶点。然而,关于内溶酶体、细胞质和细胞外液的癌细胞和组织pH值的信息尚缺。
在此,我们测量了在存在和不存在v-ATP酶抑制剂巴弗洛霉素A1的情况下U87MG细胞中的内溶酶体、细胞质和细胞外pH值。
使用LysoSensor染料和溶酶体-RFP染料进行U87MG细胞的体外测量以测定溶酶体pH值,使用BCECF-AM测定细胞质pH值,并使用pH敏感微探针测定细胞外pH值。
巴弗洛霉素A1使内溶酶体pH值从5.28升高至5.57,使细胞质pH值从7.01降至6.46,并使细胞外pH值从7.18升高至7.40。
在此,我们报告了在U87MG胶质母细胞瘤细胞中进行pH测量的能力,并在GBM发病机制和可能的治疗背景下讨论了这些结果。这对于理解GBM的发病机制可能具有一定重要性,因为内溶酶体中高度调节的氢离子储存可影响细胞质和细胞外pH值以及内溶酶体的分布、数量和大小。