Schmidt J, Casser-Bette M, Murray A B, Luz A, Erfle V
Abteilung für Molekulare Zellpathologie, Gesellschaft für Strahlen- und Umweltforschung (GSF), Neuherberg/München, Federal Republic of Germany.
Am J Pathol. 1987 Dec;129(3):503-10.
Newborn female strain NMRI mice were injected with a mouse retrovirus (OA MuLV) known to induce osteopetrosis. Primary skeletoblast cell cultures were established from humeri and calvaria of 3-day-old, 7-day-old, and 28-day-old animals. Infectious ecotropic MuLV was found in all humerus cultures from infected animals and in 7-day and 28-day calvaria cell cultures. Levels of alkaline phosphatase activity were markedly higher in cultures of calvaria and humeri from infected mice than in those from controls. In vitro infection of undifferentiated periosteal cells was followed by a decrease in cell growth and an increase in alkaline phosphatase activity. In contrast, differentiated osteoblast-like cells were barely susceptible to OA MuLV infection, and the virus did not influence their cell growth or differentiation. Electron-microscopic studies of skeletal tissue from infected old osteopetrotic mice showed virus particles associated with and budding from osteocytes and accumulated in devitalized osteocyte lacunae. The results indicate that progenitor cells of the osteoblastic lineage represent the target cells for OA MuLV in bone tissue, that virus infection induces an increase in osteoblastic activity, and that infected cells produce virus until full development of the disease.
给新生雌性NMRI品系小鼠注射一种已知可诱发骨质石化症的小鼠逆转录病毒(OA MuLV)。从3日龄、7日龄和28日龄动物的肱骨和颅骨建立原代骨母细胞培养物。在受感染动物的所有肱骨培养物以及7日龄和28日龄的颅骨细胞培养物中均发现有感染性嗜亲性MuLV。受感染小鼠的颅骨和肱骨培养物中碱性磷酸酶活性水平明显高于对照组。未分化的骨膜细胞体外感染后,细胞生长减少,碱性磷酸酶活性增加。相比之下,分化的成骨样细胞几乎不易受OA MuLV感染,且该病毒不影响其细胞生长或分化。对受感染的老龄骨质石化症小鼠的骨骼组织进行电子显微镜研究显示,病毒颗粒与骨细胞相关并从骨细胞中出芽,积聚在失活的骨细胞陷窝中。结果表明,成骨细胞系的祖细胞是骨组织中OA MuLV的靶细胞,病毒感染诱导成骨细胞活性增加,且受感染细胞在疾病充分发展之前一直产生病毒。