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少突胶质前体细胞可作为实验性胶质瘤的起源细胞。

Oligodendrocyte progenitor cells can act as cell of origin for experimental glioma.

作者信息

Lindberg N, Kastemar M, Olofsson T, Smits A, Uhrbom L

机构信息

Department of Genetics and Pathology, Uppsala University, Sweden.

出版信息

Oncogene. 2009 Jun 11;28(23):2266-75. doi: 10.1038/onc.2009.76. Epub 2009 Apr 27.

Abstract

Gliomas are primary brain tumors mainly affecting adults. The cellular origin is unknown. The recent identification of tumor-initiating cells in glioma, which share many similarities with normal neural stem cells, has suggested the cell of origin to be a transformed neural stem cell. In previous studies, using the RCAS/tv-a mouse model, platelet-derived growth factor B (PDGF-B)-induced gliomas have been generated from nestin or glial fibrillary acidic protein-expressing cells, markers of neural stem cells. To investigate if committed glial progenitor cells could be the cell of origin for glioma, we generated the Ctv-a mouse where tumor induction would be restricted to myelinating oligodendrocyte progenitor cells (OPCs) expressing 2',3'-cyclic nucleotide 3'-phosphodiesterase. We showed that PDGF-B transfer to OPCs could induce gliomas with an incidence of 33%. The majority of tumors resembled human WHO grade II oligodendroglioma based on close similarities in histopathology and expression of cellular markers. Thus, with the Ctv-a mouse we have showed that the cell of origin for glioma may be a committed glial progenitor cell.

摘要

胶质瘤是主要影响成年人的原发性脑肿瘤。其细胞起源尚不清楚。最近在胶质瘤中发现了肿瘤起始细胞,它们与正常神经干细胞有许多相似之处,这表明起源细胞是转化的神经干细胞。在先前的研究中,使用RCAS/tv-a小鼠模型,从表达神经干细胞标志物巢蛋白或胶质纤维酸性蛋白的细胞中产生了血小板衍生生长因子B(PDGF-B)诱导的胶质瘤。为了研究定向胶质祖细胞是否可能是胶质瘤的起源细胞,我们构建了Ctv-a小鼠,其中肿瘤诱导将限于表达2',3'-环核苷酸3'-磷酸二酯酶的有髓少突胶质细胞祖细胞(OPC)。我们发现,将PDGF-B转移至OPC可诱导胶质瘤,发生率为33%。基于组织病理学和细胞标志物表达的密切相似性,大多数肿瘤类似于人类世界卫生组织(WHO)二级少突胶质细胞瘤。因此,通过Ctv-a小鼠,我们表明胶质瘤的起源细胞可能是定向胶质祖细胞。

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