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叙利亚仓鼠中12型人腺病毒诱导的皮下肿瘤的细胞起源

Cell origin of human adenovirus type 12-induced subcutaneous tumor in Syrian hamsters.

作者信息

Nakajima T, Mukai N

出版信息

Acta Neuropathol. 1979 Mar 15;45(3):187-94. doi: 10.1007/BF00702670.

DOI:10.1007/BF00702670
PMID:442984
Abstract

Single subcutaneous inoculation of human adenovirus type 12 (Ad.12), 0.05-0.1 ml of 10(8.0) TCID50 HEK cells/0.1 ml, was made on the back of 0-day-old hamsters. In 21 of 25 hamsters (84.0%), multiple solid tumors developed close to the inoculation site within 3 months. No control hamsters developed tumors. Tumor histopathology revealed the characteristic Homer Wright rosettes of neuroblastoma. Ad. 12-specific tumor antigens were demonstrable in both the primary and the cultured tumor cells by the immunofluorescein technique. Histochemical demonstration of cholinesterase and NADH oxidoreductase gave rise to a predominantly positive intracytoplasmic granule within the tumor cells. Electron microscopy showed remarkably uniform cell morphology: small, undifferentiated neuroblastic cells with poorly developed intracytoplasmic organelles; many possessed characteristic solitary cilia in a 9 + 0 tubules pattern. Intercellular junctions were poorly developed. Search for an incipient tumor cell aggregate by means of immunofluorescein T-antigen detection was carried out through a 240-h period following Ad. 12 inoculation. A sequential study in parallel with electron microscopic examination of the normal subcutaneous tissue proved that neuroblastic cells closely associated with the muscle spindle anlage could preferentially become the most sensitive target for Ad. 12 tumorigenesis.

摘要

将0.05 - 0.1 ml含10(8.0) TCID50 HEK细胞/0.1 ml的人12型腺病毒(Ad.12)皮下接种于出生0天的仓鼠背部。25只仓鼠中有21只(84.0%)在3个月内在接种部位附近长出多个实体瘤。对照仓鼠未长出肿瘤。肿瘤组织病理学显示为神经母细胞瘤特有的霍纳·赖特玫瑰花结。通过免疫荧光技术在原发性肿瘤细胞和培养的肿瘤细胞中均可检测到Ad.12特异性肿瘤抗原。胆碱酯酶和NADH氧化还原酶的组织化学显示肿瘤细胞内主要为阳性的胞浆颗粒。电子显微镜显示细胞形态非常一致:小的、未分化的神经母细胞,胞浆内细胞器发育不良;许多细胞具有特征性的9 + 0微管模式的单个纤毛。细胞间连接发育不良。在Ad.12接种后的240小时内,通过免疫荧光T抗原检测寻找早期肿瘤细胞聚集物。与正常皮下组织的电子显微镜检查平行进行的一项序贯研究证明,与肌梭原基密切相关的神经母细胞可能优先成为Ad.12致瘤作用最敏感的靶点。

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