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关于急性禽白血病/肉瘤病毒所致疾病发病机制的思考,特别提及禽成红细胞增多症

Reflections on the pathogenesis of diseases caused by the acute avian leukosis/sarcoma viruses with special reference to avian erythroblastosis.

作者信息

Darcel C

机构信息

Palliser Animal Health Laboratories Ltd, Lethbridge, Alberta, Canada.

出版信息

Vet Res Commun. 1994;18(5):397-415. doi: 10.1007/BF01839290.

Abstract

The various diseases that follow experimental infection with the acute and non-acute avian oncoviruses are discussed with special reference to the pathogenesis of avian erythroblastosis. One view, based on in vitro studies, sees erythroblastosis as the product of a failure in the differentiation of virus-infected stem cells to mature erythrocytes, as a result of cell 'transformation'. The results of some in vivo studies, however, point to a resemblance of the disease to a haemolytic anaemia, where cellular death is an important component. It seems probable that the disease is the result of transformation of cells of the erythroblastic series followed by the death of many of these cells due to influences that have not yet been determined. Determination of the causes of this cellular death may prove to be as important for our understanding of the problem of leukaemia as the work that has already been accomplished in explaining the causes of cell transformation. It is also suggested that the tendency of gs amino acid sequences of the avian leukosis viruses and mouse leukaemia viruses to form fusion proteins with a variety of proto-oncogenes may be part of a wider phenomenon, and that these sequences may fuse with other proteins, altering their properties. More work is required on the possibility that there is an undiscovered immunological component in the progression of the L/S diseases.

摘要

本文特别参照禽成红细胞增多症的发病机制,探讨了急性和非急性禽肿瘤病毒实验感染后引发的各种疾病。基于体外研究的一种观点认为,成红细胞增多症是病毒感染的干细胞因细胞“转化”而无法分化为成熟红细胞的产物。然而,一些体内研究结果表明,该疾病类似于溶血性贫血,细胞死亡是其重要组成部分。这种疾病可能是成红细胞系细胞转化的结果,随后许多这些细胞因尚未明确的影响因素而死亡。确定这种细胞死亡的原因,对于我们理解白血病问题可能与已完成的解释细胞转化原因的工作同样重要。还有人提出,禽白血病病毒和小鼠白血病病毒的gs氨基酸序列与多种原癌基因形成融合蛋白的倾向,可能是更广泛现象的一部分,并且这些序列可能与其他蛋白质融合,改变其特性。对于L/S疾病进展中存在未被发现的免疫成分这一可能性,还需要开展更多研究。

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