Quantification of complement system activation by measuring C5b-9 cell surface deposition using a cell-ELISA technique

被引:17
作者
Jeon, Hyungtaek [1 ]
Lee, Ji-Su [1 ]
Yoo, Seungmin [1 ]
Lee, Myung-Shin [1 ]
机构
[1] Eulji Univ, Sch Med, Dept Microbiol & Immunol, Taejon, South Korea
基金
新加坡国家研究基金会;
关键词
Complement system; Membrane attack complex; ELISA; CANCER;
D O I
10.1016/j.jim.2014.09.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The complement system is an important aspect of immune defense against microbial invasion. Eukaiyotic cells express various complement regulatory proteins to protect them from uncontrolled complement activation. However, some eukaryotic cells possess constitutive complement system activation that does not require specific triggering factors, which is known to have unexpected effects on cell proliferation and survival. This area of research is still preliminary and a standard method to measure complement system activation in eukaryotic cells has yet to be identified. Here, we present a quantitative in vitro method to measure complement system activation in eulcaryotic cells by detecting C5b-9, the membrane attack complex, on cell surfaces. The results obtained using this assay correlated with C3b deposition measured using flow cytometry and C5b-9 deposition detected using an immunofluorescence assay. Furthermore, we showed that various cancer cell lines displayed different levels of complement system activation by using this assay. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 62
页数:6
相关论文
共 10 条
[1]   Structure of C3b reveals conformational changes that underlie complement activity [J].
Janssen, Bert J. C. ;
Christodoulidou, Agni ;
McCarthy, Andrew ;
Lambris, John D. ;
Gros, Piet .
NATURE, 2006, 444 (7116) :213-216
[2]   Mesenchymal stem cells are injured by complement after their contact with serum [J].
Li, Yan ;
Lin, Feng .
BLOOD, 2012, 120 (17) :3436-3443
[3]   Modulation of the antitumor immune response by complement [J].
Markiewski, Maciej M. ;
DeAngelis, Robert A. ;
Benencia, Fabian ;
Ricklin-Lichtsteiner, Salome K. ;
Koutoulaki, Anna ;
Gerard, Craig ;
Coukos, George ;
Lambris, John D. .
NATURE IMMUNOLOGY, 2008, 9 (11) :1225-1235
[4]   Mesenchymal Stromal Cells Engage Complement and Complement Receptor Bearing Innate Effector Cells to Modulate Immune Responses [J].
Moll, Guido ;
Jitschin, Regina ;
von Bahr, Lena ;
Rasmusson-Duprez, Ida ;
Sundberg, Berit ;
Lonnies, Lena ;
Elgue, Graciela ;
Nilsson-Ekdahl, Kristina ;
Mougiakakos, Dimitrios ;
Lambris, John D. ;
Ringden, Olle ;
Le Blanc, Katarina ;
Nilsson, Bo .
PLOS ONE, 2011, 6 (07)
[5]   Complement inhibition in cancer therapy [J].
Pio, Ruben ;
Ajona, Daniel ;
Lambris, John D. .
SEMINARS IN IMMUNOLOGY, 2013, 25 (01) :54-64
[6]   Paroxysmal Nocturnal Hemoglobinuria and the Complement System: Recent Insights and Novel Anticomplement Strategies [J].
Risitano, Antonio M. .
COMPLEMENT THERAPEUTICS, 2013, 735 :155-172
[7]   Cancer and the Complement Cascade [J].
Rutkowski, Martin J. ;
Sughrue, Michael E. ;
Kane, Ari J. ;
Mills, Steven A. ;
Parsa, Andrew T. .
MOLECULAR CANCER RESEARCH, 2010, 8 (11) :1453-1465
[8]   Mesenchymal Stem Cells Engineered to Inhibit Complement-Mediated Damage [J].
Soland, Melisa A. ;
Bego, Mariana ;
Colletti, Evan ;
Zanjani, Esmail D. ;
St Jeor, Stephen ;
Porada, Christopher D. ;
Almeida-Porada, Graca .
PLOS ONE, 2013, 8 (03)
[9]   Membrane attack by complement: the assembly and biology of terminal complement complexes [J].
Tegla, Cosmin A. ;
Cudrici, Cornelia ;
Patel, Snehal ;
Trippe, Richard, III ;
Rus, Violeta ;
Niculescu, Florin ;
Rus, Horea .
IMMUNOLOGIC RESEARCH, 2011, 51 (01) :45-60
[10]   Mesenchymal Stem Cells Derived from Human Gingiva Are Capable of Immunomodulatory Functions and Ameliorate Inflammation-Related Tissue Destruction in Experimental Colitis [J].
Zhang, Qunzhou ;
Shi, Shihong ;
Liu, Yi ;
Uyanne, Jettie ;
Shi, Yufang ;
Shi, Songtao ;
Le, Anh D. .
JOURNAL OF IMMUNOLOGY, 2009, 183 (12) :7787-7798