Lithium effects on vesicular trafficking in hepatocellular carcinoma cells

被引:2
作者
Taskaeva, Iuliia [1 ,2 ]
Bgatova, Nataliya [1 ]
Gogaeva, Izabella [1 ]
机构
[1] Russian Acad Sci, Siberian Branch, Lab Ultrastruct Res, Inst Clin & Expt Lymphol,Inst Cytol & Genet, Novosibirsk, Russia
[2] Novosibirsk State Univ, Dept Phys, Lab Boron Neutron Capture Therapy, Novosibirsk, Russia
关键词
Hepatocellular carcinoma; lithium; vesicular trafficking; endocytosis; electron microscopy; LYSOSOMAL MEMBRANE PERMEABILIZATION; ENDOCYTOSIS; CAVEOLAE; MECHANISMS; DEATH; EXPRESSION; ENDOSOMES; LEUKEMIA; RECEPTOR; PATHWAY;
D O I
10.1080/01913123.2019.1701167
中图分类号
TH742 [显微镜];
学科分类号
摘要
Hepatocellular carcinoma (HCC) is one of the most commonly malignant tumors worldwide, characterized by the presence of many heterogeneous molecular cell events that contribute to tumor growth and progression. Endocytic processes are intimately involved in various pathological conditions, including cancer, since they interface with various cellular signaling programs. The ability of lithium to induce cell death and autophagy and affect cell proliferation and intracellular signaling has been shown in various experimental tumor models. The aim of this study was to evaluate the effects of lithium on vesicular transport in hepatocellular carcinoma cells. Using transmission electron microscopy we have characterized the endocytic apparatus in hepatocellular carcinoma-29 (HCC-29) cells in vivo and detailed changes in endocytotic vesicles after 20 mM lithium carbonate administration. Immunofluorescent analysis was used to quantify cells positive for EEA1-positive early endosomes, Rab11-positive recycling endosomes and Rab7-positive late endosomes. Lithium treatment caused an increase in EEA1- and Rab11-positive structures and a decrease in Rab7-positive vesicles. Thus, lithium affects diverse endocytic pathways in HCC-29 cells which may modulate growth and development of hepatocellular carcinoma.
引用
收藏
页码:301 / 311
页数:11
相关论文
共 70 条
[11]   Endocytosis, signaling and cancer, much more than meets the eye Preface [J].
Di Fiore, Pier Paolo .
MOLECULAR ONCOLOGY, 2009, 3 (04) :273-279
[12]   Mechanisms of Endocytosis [J].
Doherty, Gary J. ;
McMahon, Harvey T. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2009, 78 :857-902
[13]   G-protein-coupled receptors and cancer [J].
Dorsam, Robert T. ;
Gutkind, J. Silvio .
NATURE REVIEWS CANCER, 2007, 7 (02) :79-94
[14]   Endocytic pathways and endosomal trafficking: a primer [J].
Elkin S.R. ;
Lakoduk A.M. ;
Schmid S.L. .
Wiener Medizinische Wochenschrift, 2016, 166 (7-8) :196-204
[15]   Lithium-mediated downregulation of PKB/Akt and cyclin E with growth inhibition in hepatocellular carcinoma cells [J].
Erdal, E ;
Ozturk, N ;
Cagatay, T ;
Eksioglu-Demiralp, E ;
Ozturk, M .
INTERNATIONAL JOURNAL OF CANCER, 2005, 115 (06) :903-910
[16]   Inhibition of GSK3 by lithium, from single molecules to signaling networks [J].
Freland, Laure ;
Beaulieu, Jean-Martin .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2012, 5
[17]   Recombinant human PDCD5 exhibits an antitumor role in hepatocellular carcinoma cells via clathrin-dependent endocytosis [J].
Fu, Da-Zhi ;
Cheng, Ying ;
He, Hui ;
Liu, Hai-Yang ;
Liu, Yong-Feng .
MOLECULAR MEDICINE REPORTS, 2015, 12 (06) :8135-8140
[18]   Caveolin-1 Is Up-Regulated by GLI1 and Contributes to GLI1-Driven EMT in Hepatocellular Carcinoma [J].
Gai, Xiaohong ;
Lu, Zhongtang ;
Tu, Kangsheng ;
Liang, Zheyong ;
Zheng, Xin .
PLOS ONE, 2014, 9 (01)
[19]   Endocytosis of Receptor Tyrosine Kinases [J].
Goh, Lai Kuan ;
Sorkin, Alexander .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2013, 5 (05)
[20]   Rab7 is required for the normal progression of the autophagic pathway in mammalian cells [J].
Gutierrez, MG ;
Munafó, DB ;
Berón, W ;
Colombo, MI .
JOURNAL OF CELL SCIENCE, 2004, 117 (13) :2687-2697