Weitz Tara M, Town Terrence
Regenerative Medicine Institute Neural Program and Department of Biomedical Sciences, Cedars-Sinai Medical Center, 8700 Beverly Boulevard, Steven Spielberg Building Room 345, Los Angeles, CA 90048, USA.
Int J Alzheimers Dis. 2012;2012:314185. doi: 10.1155/2012/314185. Epub 2012 Jun 20.
Neuroinflammation is now regarded as both an early event and prime mover in the pathobiology of Alzheimer disease (AD), a neurodegenerative disease that represents a growing public health threat. As the resident innate immune cells within the central nervous system, microglia are centrally positioned as key orchestrators of brain inflammation. It is now accepted that numerous forms of activated microglia exist. Furthermore, while some types of reactive microglia are detrimental, others can actually be beneficial. In the context of AD etiopathology, much debate surrounds whether these enigmatic cells play "good" or "bad" roles. In this article, we distill a complex clinical and experimental literature focused on the contribution of microglia to AD pathology and progression. A synthesis of the literature only seems possible when considering context- the conditions under which microglia encounter and mount immunological responses to AD pathology. In order to carry out these diverse contextual responses, a number of key receptors and signaling pathways are variously activated. It will be critically important for future studies to address molecular mediators that lead to beneficial microglial responses and therefore represent important therapeutic targets for AD.
神经炎症现在被认为是阿尔茨海默病(AD)病理生物学中的早期事件和主要推动者,AD是一种神经退行性疾病,对公众健康构成越来越大的威胁。作为中枢神经系统中的固有免疫细胞,小胶质细胞在脑炎症的关键协调中处于核心地位。现在人们公认存在多种形式的活化小胶质细胞。此外,虽然某些类型的反应性小胶质细胞是有害的,但其他类型实际上可能是有益的。在AD病因病理学的背景下,关于这些神秘细胞是起“好”作用还是“坏”作用存在很多争论。在本文中,我们提炼了复杂的临床和实验文献,这些文献聚焦于小胶质细胞对AD病理和进展的作用。只有在考虑背景——小胶质细胞遇到AD病理并对其产生免疫反应的条件时,才有可能对文献进行综合。为了进行这些不同的背景反应,许多关键受体和信号通路会被不同程度地激活。对于未来的研究来说,确定导致有益小胶质细胞反应的分子介质至关重要,因此这些介质是AD重要的治疗靶点。