Monoclonal antibody FC-5.01, directed against CD63 antigen, is internalized into cytoplasmic vesicles in the IIB-BR-G human breast cancer cell line

被引:3
作者
Barrio, MM [1 ]
Portela, P [1 ]
Mordoh, J [1 ]
机构
[1] Inst Invest Bioquim Fdn Campomar, RA-1405 Buenos Aires, DF, Argentina
来源
HYBRIDOMA | 1998年 / 17卷 / 06期
关键词
D O I
10.1089/hyb.1998.17.517
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Monoclonal antibody (MAb) FC-5.01, raised against the undifferentiated breast cancer cell line DB-BR-G, has been recently shown to react with CD63, The antigen (Ag) recognized by MAb FC-5.01 is expressed in plasma membranes of IIB-BR-G and other neoplastic cells, as well as in activated platelets and endothelial cells, as detected by indirect immunofluorescence performed at 4 degrees C on live cells. In permeabilized cells, MAb FC-5.01 colocalizes with acridine orange in acidic vesicles (lysosomal/endosomal compartment), Scatchard plot analysis performed on IB-BR-G cells demonstrated a 1.4 +/- 0.4 x 10(7) M-1 affinity constant and 2.1 x 10(6) antigenic sites per cell. MAb FC-5.01 is not able to mediate C fixation or ADCC toward CD63(+) cells, but the FC-5.01-CD63 complex is efficiently internalized into cytoplasmic vesicles, as shown by an acid wash immunofluorescence assay. Cellular catabolism of the antibody bound by IIB-BR-G cells was studied using [I-125]-FC-5.01, At 18 h, >70% of the radioactivity was present in the supernatant as degraded fragments (TCA-soluble). After internalization, rapid Ag re-expression could be demonstrated in IIB-BR-G cells. MAb FC-5.01 diminished migration of CD63(+) cells in a Boyden chamber assay. Some of the above-mentioned properties would enable the use of MAb FC-5.01 as a vehicle to target different compounds inside CD63(+) cells.
引用
收藏
页码:517 / 525
页数:9
相关论文
共 38 条
[1]   MONOCLONAL-ANTIBODY TO A HIGHLY GLYCOSYLATED PROTEIN REACTS IN FIXED TISSUE WITH MELANOMA AND OTHER TUMORS [J].
ATKINSON, B ;
ERNST, CS ;
GHRIST, BFD ;
ROSS, AH ;
CLARK, WH ;
HERLYN, M ;
HERLYN, D ;
MAUL, G ;
STEPLEWSKI, Z ;
KOPROWSKI, H .
HYBRIDOMA, 1985, 4 (03) :243-255
[2]  
AZORSA DO, 1991, BLOOD, V78, P280
[3]  
BALLARE C, 1995, CANCER IMMUNOL IMMUN, V41, P15
[4]   A new epitope on human melanoma-associated antigen CD63/ME491 expressed by both primary and metastatic melanoma [J].
Barrio, MM ;
Bravo, AI ;
Portela, P ;
Hersey, P ;
Mordoh, J .
HYBRIDOMA, 1998, 17 (04) :355-364
[5]   RECEPTOR BLOCKADE WITH MONOCLONAL-ANTIBODIES AS ANTICANCER THERAPY [J].
BASELGA, J ;
MENDELSOHN, J .
PHARMACOLOGY & THERAPEUTICS, 1994, 64 (01) :127-154
[6]   Characterization of novel complexes on the cell surface between integrins and proteins with 4 transmembrane domains (TM4 proteins) [J].
Berditchevski, F ;
Zutter, MM ;
Hemler, ME .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (02) :193-207
[7]   DESCRIPTION OF A NEW HUMAN BREAST-CANCER CELL-LINE, IIB-BR-G, ESTABLISHED FROM A PRIMARY UNDIFFERENTIATED TUMOR [J].
BOVER, L ;
BARRIO, M ;
SLAVUTSKY, I ;
BRAVO, AI ;
QUINTANS, C ;
BAGNATI, A ;
LEMA, B ;
SCHIAFFI, J ;
YOMHA, R ;
MORDOH, J .
BREAST CANCER RESEARCH AND TREATMENT, 1991, 19 (01) :47-56
[8]  
Bover L, 1998, CELL MOL BIOL, V44, P493
[9]  
BREUL SD, 1980, J BIOL CHEM, V255, P5250
[10]   FC-2.15, a monoclonal antibody active against human breast cancer, specifically recognizes Lewisx hapten [J].
Capurro, M ;
Bover, L ;
Portela, P ;
Livingston, P ;
Mordoh, J .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1998, 45 (06) :334-339