T cell acquisition of APC membrane can impact interpretation of adoptive transfer experiments using CD45 congenic mouse strains

被引:4
作者
Cho, Kathy S. [1 ]
Hill, Ann B. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Mol Microbial & Immunol, Portland, OR 97239 USA
关键词
membrane transfer; adoptive transfer; CD45; congenic; murine cytomegalovirus;
D O I
10.1016/j.jim.2007.10.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Congenic mouse strains bearing allelic variants of CD45 are often used in adoptive transfer experiments. Here, we report that immune CD8(+) splenocytes of donor origin acquired the recipient's congenic CD45 marker during interaction with antigen-bearing cells, presumably as a result of membrane transfer upon dissolution of the immunological synapse. Acquisition of recipient marker by donor cells was most prominent after in vitro incubation with peptide for intracellular cytokine staining, where most of the antigen-bearing splenocytes are of recipient origin. In consequence, when antibodies against the recipient's congenic marker were used to distinguish donor and recipient populations, donor origin cells were incorrectly interpreted as being of recipient origin. This phenomenon may cause problems for interpretation of data in adoptive transfer experiments primarily when (a) staining for the recipient's congenic marker and (b) identifying antigen-specific populations by staining for intracellular cytokine. (C) 2007 Published by Elsevier B.V.
引用
收藏
页码:137 / 145
页数:9
相关论文
共 10 条
[1]   ANTIGEN-BINDING SPECIFICITY OF ISOLATED CELL-SURFACE IMMUNOGLOBULIN FROM THYMUS-CELLS ACTIVATED TO HISTOCOMPATIBILITY ANTIGENS [J].
CONE, RE ;
SPRENT, J ;
MARCHALONIS, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (09) :2556-+
[2]   TCR-mediated internalization of peptide-MHC complexes acquired by T cells [J].
Huang, JF ;
Yang, Y ;
Sepulveda, H ;
Shi, WX ;
Hwang, I ;
Peterson, PA ;
Jackson, MR ;
Sprent, J ;
Cai, ZL .
SCIENCE, 1999, 286 (5441) :952-954
[3]   Cutting edge: CTLs rapidly capture membrane fragments from target cells in a TCR signaling-dependent manner [J].
Hudrisier, D ;
Riond, J ;
Mazarguil, H ;
Gairin, JE ;
Joly, E .
JOURNAL OF IMMUNOLOGY, 2001, 166 (06) :3645-3649
[4]   Direct cross-priming by Th lymphocytes generates memory cytotoxic T cell responses [J].
Kennedy, R ;
Undale, AH ;
Kieper, WC ;
Block, MS ;
Pease, LR ;
Celis, E .
JOURNAL OF IMMUNOLOGY, 2005, 174 (07) :3967-3977
[5]   Genome-wide analysis reveals a highly diverse CD8 T cell response to murine cytomegalovirus [J].
Munks, Michael W. ;
Gold, Marielle C. ;
Zajac, Allison L. ;
Doom, Carmen M. ;
Morello, Christopher S. ;
Spector, Deborah H. ;
Hill, Ann B. .
JOURNAL OF IMMUNOLOGY, 2006, 176 (06) :3760-3766
[6]   The immunological synapse of CTL contains a secretory domain and membrane bridges [J].
Stinchcombe, JC ;
Bossi, G ;
Booth, S ;
Griffiths, GM .
IMMUNITY, 2001, 15 (05) :751-761
[7]   Detection of virus-specific T cells and CD8+ T-cell epitopes by acquisition of peptide-HLA-GFP complexes:: analysis of T-cell phenotype and function in chronic viral infections [J].
Tomaru, U ;
Yamano, Y ;
Nagai, M ;
Maric, D ;
Kaumaya, PTP ;
Biddison, W ;
Jacobson, S .
NATURE MEDICINE, 2003, 9 (04) :469-475
[8]   Systematic excision of vector sequences from the BAC-cloned herpesvirus genome during virus reconstitution [J].
Wagner, M ;
Jonjic, S ;
Koszinowski, UH ;
Messerle, M .
JOURNAL OF VIROLOGY, 1999, 73 (08) :7056-7060
[9]   Acquisition of functional MHC class II/peptide complexes by T cells during thymic development and CNS-directed pathogenesis [J].
Walker, MR ;
Mannie, MD .
CELLULAR IMMUNOLOGY, 2002, 218 (1-2) :13-25
[10]  
Wetzel SA, 2006, CRIT REV IMMUNOL, V26, P1