Lamprey Variable Lymphocyte Receptors Mediate Complement-Dependent Cytotoxicity

被引：33

作者：

Wu, Fenfang ^{[1
,2
]}

Chen, Liyong ^{[1
,2
]}

Liu, Xin ^{[2
]}

Wang, Huaying ^{[2
]}

Su, Peng ^{[1
,2
]}

Han, Yinglun ^{[1
,2
]}

Feng, Bo ^{[1
,2
]}

Qiao, Xu ^{[1
,2
]}

Zhao, Jing ^{[1
,2
]}

Ma, Ning ^{[1
,2
]}

Liu, Huijie ^{[1
,2
]}

Zheng, Zhen ^{[1
,2
]}

Li, Qingwei ^{[1
,2
]}

机构：

[1] Liaoning Normal Univ, Coll Life Sci, Dalian 116029, Liaoning, Peoples R China

[2] Liaoning Normal Univ, Inst Marine Genom & Prote, Dalian 116029, Liaoning, Peoples R China

来源：

JOURNAL OF IMMUNOLOGY | 2013年 / 190卷 / 03期

关键词：

B-CHAIN; CLASSICAL PATHWAY; MOLECULAR-CLONING; SUBCOMPONENT C1Q; SEA LAMPREY; C-CHAINS; A-CHAINS; ACTIVATION; PROTEIN; SYSTEM;

D O I：

10.4049/jimmunol.1200876

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

An alternative adaptive-immune system is present in the most basal vertebrates-lampreys and hagfish-the only surviving jawless vertebrates. These eel-like fish use leucine-rich repeat-based receptors for Ag recognition instead of the Ig-based receptors used in jawed vertebrates. We report that in Japanese lamprey (Lampetra japonica), variable lymphocyte receptor (VLR)B interacts with C1q and C3 proteins to mediate complement-dependent cytotoxicity for bacteria and tumor cells. The immune-based lysis involves deposition of VLRB and C1q-like protein complex on the surface of target cells, activation of C3, and ultimate disruption of cell wall integrity. The demonstration of functional interaction between VLRB and complement components in lamprey provides evidence for the emergence of cooperative innate and adaptive-immune responses at a pivotal point in vertebrate evolution, before or in parallel with the evolution of Ig-based Abs and the classical complement-activation pathway. The Journal of Immunology, 2013, 190: 922-930.

引用

页码：922 / 930

页数：9

共 32 条

[1] Antibody responses of variable lymphocyte receptors in the lamprey [J].

Alder, Matthew N. ;

Herrin, Brantley R. ;

Sadlonova, Andrea ;

Stockard, Cecil R. ;

Grizzle, William E. ;

Gartland, Lanier A. ;

Gartland, G. Larry ;

Boydston, Jeremy A. ;

Turnbough, Charles L., Jr. ;

Cooper, Max D. .

NATURE IMMUNOLOGY, 2008, 9 (03) :319-327

[2] Serum killing of Ureaplasma parvum shows serovar-determined susceptibility for normal individuals and common variable immuno-deficiency patients [J].

Beeton, Michael L. ;

Daha, Mohamed R. ;

El-Shanawany, Tariq ;

Jolles, Stephen R. ;

Kotecha, Sailesh ;

Spiller, O. Brad .

IMMUNOBIOLOGY, 2012, 217 (02) :187-194

[3]

Butko P, 1999, J IMMUNOL, V163, P2761

[4] ACTIVATION OF THE ALTERNATIVE AND CLASSICAL COMPLEMENT PATHWAYS BY ENTAMOEBA-HISTOLYTICA [J].

CALDERON, J ;

SCHREIBER, RD .

INFECTION AND IMMUNITY, 1985, 50 (02) :560-565

[5] The phylogeny of the complement system and the origins of the classical pathway [J].

Dodds, Alister W. ;

Matsushita, Misao .

IMMUNOBIOLOGY, 2007, 212 (4-5) :233-243

[6] Activation of the Classical Complement Pathway by Bacillus anthracis Is the Primary Mechanism for Spore Phagocytosis and Involves the Spore Surface Protein BclA [J].

Gu, Chunfang ;

Jenkins, Sarah A. ;

Xue, Qiong ;

Xu, Yi .

JOURNAL OF IMMUNOLOGY, 2012, 188 (09) :4421-4431

[7] Dual nature of the adaptive immune system in lampreys [J].

Guo, Peng ;

Hirano, Masayuki ;

Herrin, Brantley R. ;

Li, Jianxu ;

Yu, Cuiling ;

Sadlonova, Andrea ;

Cooper, Max D. .

NATURE, 2009, 459 (7248) :796-U1

[8] Antigen recognition by variable lymphocyte receptors [J].

Han, Byung Woo ;

Herrin, Brantley R. ;

Cooper, Max D. ;

Wilson, Ian A. .

SCIENCE, 2008, 321 (5897) :1834-1837

[9] Structure and specificity of lamprey monoclonal antibodies [J].

Herrin, Brantley R. ;

Alder, Matthew N. ;

Roux, Kenneth H. ;

Sina, Christina ;

Ehrhardt, Goetz R. A. ;

Boydston, Jeremy A. ;

Turnbough, Charles L., Jr. ;

Cooper, Max D. .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (06) :2040-2045

[10]

JOINER K, 1983, J IMMUNOL, V130, P845

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