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用无辅助因子的Friend脾集落形成病毒诱导Friend红白血病早期阶段

Induction of the early stages of Friend erythroleukemia with helper-free Friend spleen focus-forming virus.

作者信息

Berger S A, Sanderson N, Bernstein A, Hankins W D

出版信息

Proc Natl Acad Sci U S A. 1985 Oct;82(20):6913-7. doi: 10.1073/pnas.82.20.6913.

Abstract

The polycythemia-inducing strain of Friend virus (FV-P) causes a multistage erythroleukemia in susceptible mice. FV-P is a complex of two viruses, a replication-competent virus [Friend murine leukemia virus (F-MuLV)] and a replication-defective spleen focus-forming virus (SFFVp). We have addressed directly the role of SFFVp in the induction of the early stages of Friend disease by constructing stocks of SFFVp free of detectable F-MuLV, using a recently described retroviral helper-cell line. These preparations are capable of inducing erythroid bursts (vBFU-E) whose inducibility, kinetics, and responsiveness to erythropoietin suggest that they are very similar, if not identical, to the vBFU-E induced by FV-P. Single injections of helper-free SFFVp had no apparent effects in vivo, although the addition of exogenous helper virus to the inoculum resulted in the induction of classic Friend disease. Increasing the effective titer by giving mice five daily virus injections resulted in the induction of splenomegaly and a large increase in the number of erythroid colony-forming units that were independent of erythropoietin. When the injections were discontinued, the spleens regressed and all the mice survived. When the injections were continued, all the mice died within 25 days of the first injection. These results demonstrate that SFFVp alone can alter the growth characteristics of erythroid progenitors and is directly responsible for the induction of vBFU-E in vitro and the erythroid hyperplasia in vivo. They also demonstrate that the initial polyclonal stage of Friend disease is reversible and can be reproduced by using preparations of SFFVp free of detectable F-MuLV.

摘要

弗氏病毒(FV-P)的红细胞增多症诱导株可在易感小鼠中引发多阶段的红白血病。FV-P是两种病毒的复合体,一种具有复制能力的病毒[弗氏鼠白血病病毒(F-MuLV)]和一种复制缺陷型脾集落形成病毒(SFFVp)。我们通过使用最近描述的逆转录病毒辅助细胞系构建不含可检测到的F-MuLV的SFFVp毒株,直接探讨了SFFVp在弗氏病早期诱导中的作用。这些制剂能够诱导红系爆式集落形成单位(vBFU-E),其诱导能力、动力学以及对促红细胞生成素的反应表明,它们与FV-P诱导的vBFU-E非常相似,甚至相同。单次注射无辅助病毒的SFFVp在体内没有明显影响,尽管在接种物中添加外源性辅助病毒会导致典型的弗氏病。通过每天给小鼠注射五次病毒来提高有效滴度,会导致脾肿大,并使与促红细胞生成素无关的红系集落形成单位数量大幅增加。当停止注射时,脾脏缩小,所有小鼠存活。当继续注射时,所有小鼠在首次注射后25天内死亡。这些结果表明,单独的SFFVp可以改变红系祖细胞的生长特性,直接负责体外vBFU-E的诱导和体内红系增生。它们还表明,弗氏病的初始多克隆阶段是可逆的,并且可以通过使用不含可检测到的F-MuLV的SFFVp制剂来重现。

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