Bautista Wendy, Lipschitz Jeremy, McKay Andrew, Minuk Gerald Y
Section of Hepatology, Department of Medicine.
Department of Surgery, ***Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, Manitoba, Canada.
Ann Hepatol. 2017 March-April;16(2):297-303. doi: 10.5604/16652681.1231590.
The inability to distinguish cancer (CSCs) from normal stem cells (NSCs) has hindered attempts to identify safer, more effective therapies for hepatocellular carcinoma (HCC). The aim of this study was to document and compare cell membrane potential differences (PDs) of CSCs and NSCs derived from human HCC and healthy livers respectively and determine whether altered GABAergic innervation could explain the differences.
Epithelial cell adhesion molecule (EpCAM) positive stem cells were isolated from human liver tissues by magnetic bead separations. Cellular PDs were recorded by microelectrode impalement of freshly isolated cells. GABAA receptor subunit expression was documented by reverse transcriptase polymerase chain reaction (RT-PCR) and immunofluorescence.
CSCs were significantly depolarized (-7.0 ± 1.3 mV) relative to NSCs (-23.0 ± 1.4 mV, p < 0.01). The depolarized state was associated with different GABAA receptor subunit expression profiles wherein phasic transmission, represented by GAGAA α3 subunit expression, was prevalent in CSCs while tonic transmission, represented by GABAA α6 subunit expression, prevailed in NSCs. In addition, GABAA subunits α3, β3, ϒ3 and δ were strongly expressed in CSCs while GABAA π expression was dominant in NSCs. CSCs and NSCs responded similarly to GABAA receptor agonists (ΔPD: 12.5 ± 1.2 mV and 11.0 ± 3.5 mV respectively).
The results of this study indicate that CSCs are significantly depolarized relative to NSCs and these differences are associated with differences in GABAA receptor subunit expression. Together they provide new insights into the pathogenesis and possible treatment of human HCC.
无法区分癌症干细胞(CSCs)与正常干细胞(NSCs)阻碍了人们为肝细胞癌(HCC)寻找更安全、更有效治疗方法的努力。本研究的目的是记录并比较分别源自人类肝癌组织和健康肝脏的CSCs与NSCs的细胞膜电位差异(PDs),并确定γ-氨基丁酸能神经支配的改变是否可以解释这些差异。
通过磁珠分离法从人类肝脏组织中分离出上皮细胞黏附分子(EpCAM)阳性干细胞。通过微电极刺入新鲜分离的细胞来记录细胞的PDs。通过逆转录聚合酶链反应(RT-PCR)和免疫荧光法记录γ-氨基丁酸A(GABAA)受体亚基的表达。
与NSCs(-23.0±1.4 mV,p<0.01)相比,CSCs显著去极化(-7.0±1.3 mV)。去极化状态与不同的GABAA受体亚基表达谱相关,其中以GAGAAα3亚基表达为代表的相位传递在CSCs中普遍存在,而以GABAAα6亚基表达为代表的紧张性传递在NSCs中占主导。此外,GABAA亚基α3、β3、γ3和δ在CSCs中强烈表达,而GABAAπ表达在NSCs中占主导。CSCs和NSCs对GABAA受体激动剂的反应相似(ΔPD:分别为12.5±1.2 mV和11.0±3.5 mV)。
本研究结果表明,CSCs相对于NSCs显著去极化,这些差异与GABAA受体亚基表达的差异有关。它们共同为人类HCC的发病机制和可能的治疗提供了新的见解。