van Wageningen Thecla A, Gerrits Emma, Brouwer Nieske, Brevé John J P, Geurts Jeroen J G, Eggen Bart J L, Boddeke H W G M Erik, van Dam Anne-Marie
Department of Anatomy & Neurosciences, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Department of Biomedical Sciences of Cells & Systems, Section Molecular Neurobiology, University Medical Center Groningen, Groningen, The Netherlands.
Brain Commun. 2022 Jan 17;4(2):fcac005. doi: 10.1093/braincomms/fcac005. eCollection 2022.
Demyelination of the central nervous system is a prominent pathological hallmark of multiple sclerosis and affects both white and grey matter. However, demyelinated white and grey matter exhibit clear pathological differences, most notably the presence or absence of inflammation and activated glial cells in white and grey matter, respectively. In order to gain more insight into the differential pathology of demyelinated white and grey matter areas, we micro-dissected neighbouring white and grey matter demyelinated areas as well as normal-appearing matter from leucocortical lesions of human post-mortem material and used these samples for RNA sequencing. Our data show that even neighbouring demyelinated white and grey matter of the same leucocortical have a distinct gene expression profile and cellular composition. We propose that, based on their distinct expression profile, pathological processes in neighbouring white and grey matter are likely different which could have implications for the efficacy of treating grey matter lesions with current anti-inflammatory-based multiple sclerosis drugs.
中枢神经系统脱髓鞘是多发性硬化症的一个显著病理特征,会影响白质和灰质。然而,脱髓鞘的白质和灰质表现出明显的病理差异,最显著的是白质和灰质中分别存在或不存在炎症和活化的神经胶质细胞。为了更深入了解脱髓鞘白质和灰质区域的差异病理学,我们从人类尸检材料的白质皮质病变中显微切割相邻的白质和灰质脱髓鞘区域以及外观正常的组织,并将这些样本用于RNA测序。我们的数据表明,即使是来自同一白质皮质的相邻脱髓鞘白质和灰质也具有不同的基因表达谱和细胞组成。我们认为,基于它们不同的表达谱,相邻白质和灰质中的病理过程可能不同,这可能会影响目前基于抗炎的多发性硬化症药物治疗灰质病变的疗效。