Graeber Manuel B, Scheithauer Bernd W, Kreutzberg Georg W
Department of Neuropathology, Faculty of Medicine, Imperial College, London, United Kingdom.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Glia. 2002 Nov;40(2):252-259. doi: 10.1002/glia.10147.
Microglia have long been ignored by neurooncologists. This has changed with the realization that microglial cells not only occur within and around brain tumors but also contribute significantly to the actual tumor mass, notably in astrocytic gliomas. In addition, it has been speculated that microglia could play a role in the defense against neoplasms of the nervous system. However, the biological success of these tumors, i.e., their highly malignant behavior, indicates that natural microglial defense mechanisms do not function properly in astrocytomas. In fact, there is evidence that microglial behavior is controlled by tumor cells, supporting their growth and infiltration. This unexpected "Achilles heel" of microglial immune defense illustrates the risk of generalizing on the basis of a single aspect of microglial biology. Microglia are highly plastic cells, capable of exerting cytotoxic functions under conditions of CNS infections, but not necessarily during glioma progression. Thus, the suggestion that microglial activation through stimulation by cytokines (e.g., interferon-gamma) will benefit patients with brain tumors could prove fatally wrong. Therapeutic recruitment of microglia to treat such diffusely infiltrative brain tumors as astrocytic gliomas must be considered premature.
长期以来,小胶质细胞一直被神经肿瘤学家忽视。随着人们认识到小胶质细胞不仅存在于脑肿瘤内部和周围,而且对实际的肿瘤块有显著贡献,尤其是在星形胶质细胞瘤中,这种情况已经发生了改变。此外,有人推测小胶质细胞可能在抵御神经系统肿瘤方面发挥作用。然而,这些肿瘤在生物学上的成功,即它们的高度恶性行为,表明天然的小胶质细胞防御机制在星形细胞瘤中不能正常发挥作用。事实上,有证据表明小胶质细胞的行为受肿瘤细胞控制,促进其生长和浸润。小胶质细胞免疫防御这一意想不到的“阿喀琉斯之踵”说明了基于小胶质细胞生物学的某一个方面进行概括的风险。小胶质细胞是高度可塑性的细胞,在中枢神经系统感染的情况下能够发挥细胞毒性功能,但在胶质瘤进展过程中不一定如此。因此,通过细胞因子(如干扰素-γ)刺激激活小胶质细胞会使脑肿瘤患者受益这一观点可能被证明是致命错误的。将小胶质细胞用于治疗星形胶质细胞瘤等弥漫性浸润性脑肿瘤的疗法必须被认为是为时过早的。