## Abstract The number of cells from which tumors induced by neonatal injection of Rauscher Leukemia virus (RLV) develop was investigated using F~1~ (C57BL/6 X Feral) female mice heterozygous at the Xβlinked phosphoglycerate kinase (PGK) locus. Because of inactivation of one of the two X chromosome
Inhibition by streptovaricins of rauscher leukemia virus splenomegaly
β Scribed by Ernest C. Borden; William A. Carter; Lyle L. Sensenbrenner; Albert H. Owens; Judith Lichtenstein; Gary D. Gray; Gary L. Neil; F. Richard Nichol; L. H. Li
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- French
- Weight
- 560 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Streptovaricins (Sv), ansa macrolide antibiotics, inhibited Rauscher leukemia virus (RLV) splenomegaly by 25β50%. All streptovaricins tested were effective when administered orally either by diet ad lib or by intubation from infection to time of killing. When delivered by intubation, Sv wus measurable in plasma. For up to 6h. SvC, at 300 mglkglday, reduced mean splecln weight of infected mice, from 478Β±51 (SE) mg to 300555 (SE) mg. Rijampicin, at 250 mglkglday, had no similar activity. Decrease in caloric intake and in bodyβweight gain also resulted in an inhibition of RL V splenomegaly; although Svβtreated mice gained weight, the increase was usually slightly less than controls. However, mice treated with a Sv diet for a week prior to infection, after an initial period of weight loss, gained at a rate equivalent to a controlgroup, and when killed had a marked reduction in splenomegaly. The selectivity of streptovaricins and specificity for viral events was suggested by several observations: (I) Splenomegaly and mortality, induced by L1210 or a nonβinjective transplantable tumor of RL V oriAjin, was not inhibited. (2) No inhibition of normal hematopoietic spleen colonies was observed. (3) Host immune responses, including cellular and humoral immunity and interjeron production and action, were not inhibited. Thus, although the effect of slightly decreased weight and intake could not be unequivocally established, the findings were most compatible with a selective inhibition of RL V splenomegaly by Sv.
π SIMILAR VOLUMES
## Abstract Three cell lines were established in vitro from myeloid leukemias of C57Bl/6 strain mice which had been inoculated with Rauscher virus at birth. The use of heated conditioned medium from peritoneum proved helpful for the initial growth of leukemic cells. At early in vitro passage levels
The protective effect of phenylhydrazine pretreatment seen in Rauscher leukemia virus-infected intact mice is not observed when splenectomized mice are used. Such mice succumb to infection even earlier than viral potency controls. Since phenylhydrazine is known to increase both splenic erythropoiesi
## Abstract Plasma membranes purified from RBLβ5 leukemia cells and solubilized with Na deoxycholate were fractionated on an Ultrogel AcA34 column. Fractions containing most of the tumorβrejection activity but low amounts of gp70 and p30 were consolidated and used to hyperimmunize semisyngeneic, CB
## Abstract Genetic control of splenomegaly which occurs at a late stage of Friend leukemia virus infection was studied in hybrid mice between DDDβFv^r^ and C57BL/6. It was demonstrated that this late splenomegaly was mainly controlled by a single autosomal locus with the dominant allele for resist