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Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, 3 Pasteur St., 02-093 Warsaw, Poland.
Acta Neurobiol Exp (Wars). 2008;68(4):526-34. doi: 10.55782/ane-2008-1720.
Despite the numerous reports on the role of tumor necrosis factor-alpha (TNF-alpha) in the brain neuropathology, very little is known about the mechanisms by which TNF-alpha may mediate neuroprotection. Different hypotheses pertain to the molecular and cellular effectors triggered by the activation of TNF receptors (TNFRI and TNFR2). They are focused on diminishing the production of nitric oxide and free radicals, alteration of excitatory amino acids neurotransmission, maintenance of neuronal calcium homeostasis and induction of neurotrophic factors synthesis. In this review all these data are summarized. Moreover, possible explanations for the inconsistent data concerning the TNF-alpha effect on neuron are discussed.
尽管有大量关于肿瘤坏死因子-α(TNF-α)在脑神经病学中作用的报道,但对于TNF-α介导神经保护的机制却知之甚少。不同的假说是关于TNF受体(TNFRI和TNFR2)激活所触发的分子和细胞效应器。这些假说聚焦于减少一氧化氮和自由基的产生、改变兴奋性氨基酸神经传递、维持神经元钙稳态以及诱导神经营养因子合成。在这篇综述中,所有这些数据都进行了总结。此外,还讨论了关于TNF-α对神经元作用的数据不一致的可能解释。