Department of Molecular Cell Biology and Immunology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.
Department of Pathology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.
J Alzheimers Dis. 2017;60(3):795-807. doi: 10.3233/JAD-160551.
The majority of patients with Alzheimer's disease (AD) exhibit amyloid-β (Aβ) deposits at the brain vasculature, a process referred to as cerebral amyloid angiopathy (CAA). In over 51% of AD cases, Aβ also accumulates in cortical capillaries, which is termed capillary CAA (capCAA). It has been postulated that the presence of capCAA in AD is a specific subtype of AD, although underlying mechanisms are not yet fully understood. Sphingolipids (SLs) are implicated in neurodegenerative disorders, including AD. However, to date it remains unknown whether alterations in the SL pathway are involved in capCAA pathogenesis and if these differ from AD.
To determine whether AD cases with capCAA have an altered SL profile compared to AD cases without capCAA.
Immunohistochemistry was performed to assess the expression and localization of ceramide, acid sphingomyelinase (ASM), and sphingosine-1-phosphate receptors (S1P1, S1P3). In addition, we determined the concentrations of S1P as well as different chain-lengths of ceramides using HPLC-MS/MS.
Immunohistochemical analysis revealed an altered expression of ceramide, ASM, and S1P receptors by reactive astrocytes and microglial cells specifically associated with capCAA. Moreover, a shift in the balance of ceramides with different chain-lengths and S1P content is observed in capCAA.
Here we provide evidence of a deregulated SL balance in capCAA. The increased levels of ASM and ceramide in activated glia cells suggest that the SL pathway is involved in the neuroinflammatory response in capCAA pathogenesis. Future research is needed to elucidate the role of S1P in capCAA.
大多数阿尔茨海默病(AD)患者的大脑血管中存在淀粉样β(Aβ)沉积,这一过程称为脑淀粉样血管病(CAA)。在超过 51%的 AD 病例中,Aβ也会在皮质毛细血管中积累,这被称为毛细血管 CAA(capCAA)。有人推测,AD 中存在 capCAA 是 AD 的一种特定亚型,尽管其潜在机制尚未完全阐明。神经退行性疾病,包括 AD,都与鞘脂(SL)有关。然而,迄今为止,尚不清楚 SL 途径的改变是否参与了 capCAA 的发病机制,以及这些改变是否与 AD 不同。
确定是否存在 capCAA 的 AD 病例与不存在 capCAA 的 AD 病例相比具有改变的 SL 谱。
通过免疫组织化学评估神经胶质细胞中神经酰胺、酸性鞘磷脂酶(ASM)和鞘氨醇-1-磷酸受体(S1P1、S1P3)的表达和定位。此外,我们使用 HPLC-MS/MS 测定 S1P 以及不同链长神经酰胺的浓度。
免疫组织化学分析显示,与 capCAA 相关的反应性星形胶质细胞和小胶质细胞中神经酰胺、ASM 和 S1P 受体的表达发生改变。此外,在 capCAA 中观察到不同链长神经酰胺和 S1P 含量的平衡发生转移。
我们提供了 capCAA 中 SL 平衡失调的证据。激活的神经胶质细胞中 ASM 和神经酰胺水平升高表明,SL 途径参与了 capCAA 发病机制中的神经炎症反应。需要进一步的研究来阐明 S1P 在 capCAA 中的作用。