Ali Moussa Houda Yasmine, Manaph Nimshitha, Ali Gowher, Maacha Selma, Shin Kyung Chul, Ltaief Samia M, Gupta Vijay, Tong Yongfeng, Ponraj Janarthanan, Salloum-Asfar Salam, Mansour Said, Al-Shaban Fouad A, Kim Hyung-Goo, Stanton Lawrence W, Grivel Jean-Charles, Abdulla Sara A, Al-Shammari Abeer R, Park Yongsoo
Neurological Disorders Research Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Deep Phenotyping Core, Research Branch, Sidra Medicine, Doha, Qatar.
Front Integr Neurosci. 2022 May 17;16:879832. doi: 10.3389/fnint.2022.879832. eCollection 2022.
Extracellular vesicles (EVs) are membrane vesicles released from cells to the extracellular space, involved in cell-to-cell communication by the horizontal transfer of biomolecules such as proteins and RNA. Because EVs can cross the blood-brain barrier (BBB), circulating through the bloodstream and reflecting the cell of origin in terms of disease prognosis and severity, the contents of plasma EVs provide non-invasive biomarkers for neurological disorders. However, neuronal EV markers in blood plasma remain unclear. EVs are very heterogeneous in size and contents, thus bulk analyses of heterogeneous plasma EVs using Western blot and ELISA have limited utility. In this study, using flow cytometry to analyze individual neuronal EVs, we show that our plasma EVs isolated by size exclusion chromatography are mainly CD63-positive exosomes of endosomal origin. As a neuronal EV marker, neural cell adhesion molecule (NCAM) is highly enriched in EVs released from induced pluripotent stem cells (iPSCs)-derived cortical neurons and brain organoids. We identified the subpopulations of plasma EVs that contain NCAM using flow cytometry-based individual EV analysis. Our results suggest that plasma NCAM-positive neuronal EVs can be used to discover biomarkers for neurological disorders.
细胞外囊泡(EVs)是从细胞释放到细胞外空间的膜性囊泡,通过蛋白质和RNA等生物分子的水平转移参与细胞间通讯。由于EVs能够穿过血脑屏障(BBB),在血液中循环,并在疾病预后和严重程度方面反映其起源细胞,血浆EVs的内容物为神经疾病提供了非侵入性生物标志物。然而,血浆中的神经元EV标志物仍不明确。EVs在大小和内容物方面非常异质性,因此使用蛋白质免疫印迹法(Western blot)和酶联免疫吸附测定(ELISA)对异质性血浆EVs进行整体分析的效用有限。在本研究中,我们使用流式细胞术分析单个神经元EVs,结果表明,通过尺寸排阻色谱法分离的血浆EVs主要是内体来源的CD63阳性外泌体。作为一种神经元EV标志物,神经细胞黏附分子(NCAM)在诱导多能干细胞(iPSCs)衍生的皮质神经元和脑类器官释放的EVs中高度富集。我们使用基于流式细胞术的单个EV分析确定了含有NCAM的血浆EVs亚群。我们的结果表明,血浆中NCAM阳性的神经元EVs可用于发现神经疾病的生物标志物。