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小鼠B细胞白血病(BCL1):通过抗独特型抗体荧光分析确定的器官分布及生长动力学

Murine B cell leukemia (BCL1): organ distribution and kinetics of growth as determined by fluorescence analysis with an anti-idiotypic antibody.

作者信息

Krolick K A, Isakson P C, Uhr J W, Vitetta E S

出版信息

J Immunol. 1979 Nov;123(5):1928-35.

PMID:385772
Abstract

The life history of a transplantable B cell leukemia (BCL1) that arose spontaneously in a BALB/c mouse is described. Animals bearing this tumor live from 2 to 4 months in apparently good health despite massive splenomegaly and leukemia. Antibody to the idiotype or gamma light chain of the tumor IgM was used in conjunction with the fluorescence-activated cell sorter to identify tumor cells in the BCL1-bearing mice. The results suggest that these cells multiply and differentiate in the spleen and subsequently emigrate to the blood. Tumor cells do not recirculate as evidenced by their failure to enter the thoracic duct or to infiltrate lymph nodes to a significant extent. During tumor growth, a population of T cell blasts appears that may be involved with an immune response against the tumor.

摘要

描述了一种在BALB/c小鼠中自发产生的可移植性B细胞白血病(BCL1)的生命历程。携带这种肿瘤的动物尽管脾脏肿大和患有白血病,但仍能健康存活2至4个月。将针对肿瘤IgM独特型或γ轻链的抗体与荧光激活细胞分选仪结合使用,以鉴定携带BCL1的小鼠体内的肿瘤细胞。结果表明,这些细胞在脾脏中增殖和分化,随后迁移到血液中。肿瘤细胞不会再循环,这可通过它们未能进入胸导管或在很大程度上浸润淋巴结得到证明。在肿瘤生长过程中,会出现一群T细胞母细胞,它们可能参与针对肿瘤的免疫反应。

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