Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy
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Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy
Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy
解放军医学杂志(英文版)1993年第4期 页码:319-325
Affiliations:
1. Laboratory of Gastroenterology Xijing Hospital
2. Fourth Military Medical University
3. ,Xi’an,710032
Author bio:
Funds:
The project supported by National Natural Science Foundation of China No.39100053
DOI:
中图分类号:
纸质出版:1993
Accepted:
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Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy[J]. 解放军医学杂志(英文版), 1993,(4):319-325.
[1]王福安,黎松,丁杰,张学庸.Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy[J].Journal of Medical Colleges of PLA,1993(04):319-325.
Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy[J]. 解放军医学杂志(英文版), 1993,(4):319-325.DOI:
[1]王福安,黎松,丁杰,张学庸.Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy[J].Journal of Medical Colleges of PLA,1993(04):319-325.DOI:
Endocytosis of immuno-ricin A chain specific for gastric cancer and its implications in antibody targeting therapy
摘要
Abstract
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正
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In the present study
ricin A chain(RTA)was first biotinylated
and then chemicallyintroduced to a monoclonal antibody against gastric cancer
MGb
2
to generate an immuno-ricin Achain conjugate(I-RTA)specific for gastric cancer.Subsequently
its endocytosis in human gas-tric cancer cell line SGC-7901 was investigated by double dynamic EM labeling technique utilizingstreptavidin-gold and sheep anti-mouse IgG-gold probes.In addition
the effects of verapamil onI-RTA endocytosis process were also observed.Our findings demonstrated that the main entryroute of I-RTA was non-coated microinvagination
followed by coated pits and interiorization ofmicrovilli.Intracellularly
the endocytosed I-RTA was quickly transported from tubulovesicularstrueutres to multivesicular bodies
and finally to lysosomes where it was degraded
while in thenon-membranous structures I-RTA was scanty.In the presence of verapamil
however
I-RTAwas found to stay longer in tubulovesicular structures and to move in a less amount and moreslowly into lysosomes.In the meantime
I-RTA was seen to be increased in the non-membranousstructures of the cytosol
and the in vitro killing efficacy was greatly augmented.
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