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关于梅森- Pfizer猴病毒诱导人角质形成细胞多核体形成的研究。

Studies on human KC cell syncytia formation induced by Mason-Pfizer monkey virus.

作者信息

Ogura H, Oda T

出版信息

Acta Med Okayama. 1977 Aug;31(4):243-7.

PMID:145160
Abstract

Human KC cell monolayer inoculated with concentraten Mason-Pfizer monkey virus (MPMV) showed syncytia formation within an hour. The cell fusion was blocked by the treatment of the MPMV with neutralizing antiserum. Treatment of the MPVM with beta-propiolactone resulted in the loss of infectivity although KC cell fusion ability of the virus still remained. KC cells inoculated with unconcentrated MPMV showed no cell fusion even after several transfers, although a chronic MPMV infection was established. The virus-producing KC cells were refractory to fusion by MPMV. Human embryonic lung cells (HEL) were infected by serially diluted MPMV harvested from virus-producing culture, transferred twice, then cultivated together with KC cells for syncytia formation to examine the end point dilution titer of the virus. HEL infected by 10(-4)-diluted MPMV still induced syncytia formation by cocultivation with KC cells.

摘要

接种浓缩马森 - 辉瑞猴病毒(MPMV)的人角质形成细胞(KC)单层在一小时内出现多核巨细胞形成。用中和抗血清处理MPMV可阻断细胞融合。用β-丙内酯处理MPVM导致其失去感染性,尽管该病毒的KC细胞融合能力仍然存在。接种未浓缩MPMV的KC细胞即使经过几次传代也未显示细胞融合,尽管已建立了慢性MPMV感染。产生病毒的KC细胞对MPMV诱导的融合具有抗性。用从产生病毒的培养物中收获的系列稀释MPMV感染人胚肺细胞(HEL),传代两次,然后与KC细胞一起培养以形成多核巨细胞,以检测病毒的终点稀释效价。被10(-4)稀释的MPMV感染的HEL与KC细胞共培养时仍诱导多核巨细胞形成。

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