Amici C, Oppi C, Fiorucci G, Battistini A, Djaczenko W, Elia G, Rossi G B, Benedetto A
Arch Virol. 1987;92(1-2):151-64. doi: 10.1007/BF01310069.
The replication of Friend Leukemia virus (FLV) has been investigated in adhesive clones (FF) of Friend Leukemia cells which were selected via cultivation on top of human fibroblast monolayers. In these adhesive clones a shut-down of FLV production is observed under conditions of culture confluency; this finding is not due either to a reduced number of cell divisions nor to a defective expression of FLV genome as assessed by Northern blot and immunofluorescence studies. Ultrastructural studies showed that virus budding and release into the medium is not detectable under these conditions. Conversely, in confluent FF cell monolayers abundant imperfect type-A enveloped particles were visible, possibly originating from stacks of granular endoplasmic reticulum with thickened membranes. It is postulated that the reduced virus production in adhesive FF monolayers is due to as yet undetermined events taking place during virus maturation at a time coincident with that of cell-cell adhesion under conditions of culture confluency.
已在通过在人成纤维细胞单层上培养而筛选出的弗氏白血病细胞的黏附克隆(FF)中研究了弗氏白血病病毒(FLV)的复制情况。在这些黏附克隆中,在培养汇合的条件下观察到FLV产生的停止;通过Northern印迹和免疫荧光研究评估,这一发现既不是由于细胞分裂数量减少,也不是由于FLV基因组表达缺陷所致。超微结构研究表明,在这些条件下无法检测到病毒出芽并释放到培养基中。相反,在汇合的FF细胞单层中可见大量不完美的A型包膜颗粒,可能源自膜增厚的颗粒内质网堆叠。据推测,黏附的FF单层中病毒产生减少是由于在培养汇合条件下与细胞间黏附同时发生的病毒成熟过程中尚未确定的事件所致。