Expression of costimulatory molecules in human neuroblastoma. Evidence that CD40+neuroblastoma cells undergo apoptosis following interaction with CD40L

被引:31
|
作者
Airoldi, I
Lualdi, S
Bruno, S
Raffaghello, L
Occhino, M
Gambini, C
Pistoia, V
Corrias, M
机构
[1] Ist Giannina Gaslini, Lab Oncol, I-16148 Genoa, Italy
[2] Ist Giannina Gaslini, Serv Pathol, I-16148 Genoa, Italy
[3] Univ Genoa, Dept Expt Med, Sect Human Anat, Genoa, Italy
关键词
costimulatory molecules; human neuroblastoma; CD40; apoptosis; caspase-8;
D O I
10.1038/sj.bjc.6600951
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumour cells display low to absent expression of costimulatory molecules. Here, we have investigated the expression of costimulatory molecules (CD40, CD80, CD86, PD-1L, B7H2, OX40L and 4-1BBL) in human neuroblastoma ( NB) cells, since virtually no information is available on this issue. Both established NB cell lines and primary tumours were tested by RT - PCR and flow cytometry. Neuroblastoma cell lines expressed the transcripts of all costimulatory molecule genes, but not the corresponding proteins. Culture of NB cell lines with human recombinant (r) IFN-gamma induced surface expression of CD40 in half of them. Primary NB cells showed CD40, CD80, CD86, OX40L, 4-1BBL, but not PD-1L and B7H2, mRNA expression. Surface CD40 was consistently detected on primary NB cells by flow cytometry. Interferon-gamma gene-transfected NB cells expressed constitutively surface CD40 and were induced into apoptosis by incubation with rCD40L through a caspase-8-dependent mechanism. CD40 may represent a novel therapeutic target in NB.
引用
收藏
页码:1527 / 1536
页数:10
相关论文
共 50 条
  • [31] Induction of β-chemokine secretion by human brain microvessel endothelial cells via CD40/CD40L interactions
    Omari, KM
    Chui, R
    Dorovini-Zis, K
    JOURNAL OF NEUROIMMUNOLOGY, 2004, 146 (1-2) : 203 - 208
  • [32] Quantitation of low level CD40L expression on resting CD4+ve cells
    Whale, K.
    Mason, S.
    Fosatti, G.
    Shock, A.
    IMMUNOLOGY, 2010, 131 : 164 - 164
  • [33] Individual and epistatic effects of genetic polymorphisms of the B cell costimulatory molecules CD40L, CD40 and BLYS but not of CD19 on endemic pemphigus foliaceus disease susceptibility
    Malheiros, Danielle
    Petzl-Erler, Maria-Luiza
    TISSUE ANTIGENS, 2009, 73 (05): : 406 - 406
  • [34] Identification and characterization of CD8+T helper cells based on CD40L expression
    Frentsch, Marco
    Stark, Regina
    Listopad, Joanna
    Meier, Sarah
    Schulz, Axel
    Durlanik, Sibel
    Blankenstein, Thomas
    Thiel, Andreas
    JOURNAL OF IMMUNOLOGY, 2011, 186
  • [35] Expression of CD40L on CD8 T cells and its role in influenza A infection
    Tay, Neil
    Padubidhri, Nayana Prabhu
    Wong, Hok Sum
    Chua, Yen
    Kemeny, David
    JOURNAL OF IMMUNOLOGY, 2015, 194
  • [36] CD40/CD40L interaction prevents CD4+ T cell anergy following HSV-1 infection.
    Hendricks, RL
    Xu, M
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2001, 42 (04) : S42 - S42
  • [37] Xenogeneic interaction between human CD40L and porcine CD40 activates porcine endothelial cells through NF-κB signaling
    Choi, Inho
    Kim, Sung Dae
    Cho, Bumrae
    Kim, Donghee
    Park, Dongkyoo
    Koh, Yun Sook
    Kim, Bo-Yoon
    Kim, Jae Young
    Yang, Jaeseok
    Ahn, Curie
    MOLECULAR IMMUNOLOGY, 2008, 45 (02) : 575 - 580
  • [38] CD40 expression on graft infiltrates and parenchymal CD154 (CD40L) induction in human chronic renal allograft rejection
    Gaweco, AS
    Mitchell, BL
    Lucas, BA
    McClatchey, KD
    Van Thiel, DH
    KIDNEY INTERNATIONAL, 1999, 55 (04) : 1543 - 1552
  • [39] CAR T Cells Express CD40L and Activates Human Dendritic Cells
    Karlsson, Hannah
    Gustafsson, Wictor
    Stromberg, Ulla Olsson
    Savoldo, Barbara
    Dotti, Gianpietro
    Loskog, Angelica
    MOLECULAR THERAPY, 2014, 22 : S61 - S61
  • [40] CD40L expression is sustained on activated T cells by CD28-dependent IL-2 production: role of CD40L in B cell help.
    Lee, B
    Haynes, L
    Swain, S
    Lund, F
    Randall, T
    FASEB JOURNAL, 2001, 15 (04): : A344 - A344