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Tumor metastases and cell-mediated immunity in a model system in DBA/2 mice. VIII. Expression and shedding of Fcγ receptors on metastatic tumor cell variants

✍ Scribed by Schirrmacher, Volker ;Jacobs, Wolfgang


Publisher
Wiley (John Wiley & Sons)
Year
1979
Tongue
English
Weight
687 KB
Volume
11
Category
Article
ISSN
0091-7419

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✦ Synopsis


The expression of receptors for the Fc portion of IgG immunoglobin molecules was studied on tumor cell lines with high and low metastatic capacity. Two tumor cell lines from DBA/2 mice that had high metastatic activity, ESb and MDAY-D2, contained a high percentage of Fc receptor positive cells, as detected in a rosette assay with IgG antibody-coated erythrocytes (EA). In contrast, the low metastatic parental line Eb, from which ESb was derived, contained only a low percentage of EA-rosette-forming cells. ESb ascites tumor cells adapted t o tissue culture in the presence of 2mercaptoethanol (2ME) had a high expression of Fc receptors, whereas a cell line adapted t o tissue culture in the absence of 2ME had a low expression of Fc receptors.

t o cause blocking of rosette formation. They were found to be present in fluids from tumor-bearing animals, such as serum and cell-free ascites. Even animals with an ascites tumor of the low-metastatic line Eb contained "soluble" Fc receptors.

The results are discussed with regard t o their possible significance for tumor metastasis.

"Soluble" Fc receptors were detectable by their ability t o bind t o EA and

Key words: tumor metastases, Fc receptor, shedding, tumor variants

Properties of tumor cells that may be impor lant for tumor cell dissemination and formation of metastasis are investigated in a syngeneic tumor model system in DBA/2 mice. The system consists of a methylcholanthrene-induced lymphoma (Eb) with low metastatic potential and a spontaneous variant thereof (ESb) with high metastatic capability. An unrelated methylcholanthrene-induced tumor (MDAY-D2) with pronounced metastasizing capacity is included for comparison. The major characteristics of these tumor cells have already been described [ 1-41 and are summarized in Table I. We showed


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