Kato Yukino, Tago Kenji, Fukatsu Shoya, Okabe Miyu, Shirai Remina, Oizumi Hiroaki, Ohbuchi Katsuya, Yamamoto Masahiro, Mizoguchi Kazushige, Miyamoto Yuki, Yamauchi Junji
Laboratory of Molecular Neurology, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
Department of Biochemistry, Jichi Medical University, Tochigi 321-0498, Japan.
Noncoding RNA. 2022 Jun 6;8(3):42. doi: 10.3390/ncrna8030042.
Angiotensin-converting enzyme 2 (ACE2) plays a role in catalyzing angiotensin II conversion to angiotensin (1-7), which often counteracts the renin-angiotensin system. ACE2 is expressed not only in the cells of peripheral tissues such as the heart and kidney, but also in those of the central nervous system (CNS). Additionally, ACE2 acts as the receptor required for the entry of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), whose binding leads to endocytotic recycling and possible degradation of the ACE2 proteins themselves. One of the target cells for SARS-CoV-2 in the CNS is oligodendrocytes (oligodendroglial cells), which wrap neuronal axons with their differentiated plasma membranes called myelin membranes. Here, for the first time, we describe the role of ACE2 in FBD-102b cells, which are used as the differentiation models of oligodendroglial cells. Unexpectedly, RNA knockdown of ACE2 with CasRx-mediated gRNA or the cognate siRNA promoted oligodendroglial cell morphological differentiation with increased expression or phosphorylation levels of differentiation and/or myelin marker proteins, suggesting the negative role of ACE2 in morphological differentiation. Notably, ACE2's intracellular region preferentially interacted with the active GTP-bound form of Ras. Thus, knockdown of ACE2 relatively increased GTP-bound Ras in an affinity-precipitation assay. Indeed, inhibition of Ras resulted in decreasing both morphological differentiation and expression or phosphorylation levels of marker proteins, confirming the positive role of Ras in differentiation. These results indicate the role of ACE2 itself as a negative regulator of oligodendroglial cell morphological differentiation, newly adding ACE2 to the list of regulators of oligodendroglial morphogenesis as well as of Ras-binding proteins. These findings might help us to understand why SARS-CoV-2 causes pathological effects in the CNS.
血管紧张素转换酶2(ACE2)在催化血管紧张素II转化为血管紧张素(1-7)过程中发挥作用,而血管紧张素(1-7)通常会对抗肾素-血管紧张素系统。ACE2不仅在心脏和肾脏等外周组织的细胞中表达,也在中枢神经系统(CNS)的细胞中表达。此外,ACE2是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)进入细胞所需的受体,SARS-CoV-2与之结合会导致内吞再循环以及ACE2蛋白本身可能的降解。CNS中SARS-CoV-2的靶细胞之一是少突胶质细胞(少突胶质细胞),它们用其分化的质膜(称为髓鞘膜)包裹神经元轴突。在此,我们首次描述了ACE2在FBD-102b细胞中的作用,FBD-102b细胞用作少突胶质细胞的分化模型。出乎意料的是,用CasRx介导的gRNA或同源siRNA对ACE2进行RNA敲低促进了少突胶质细胞的形态分化,同时分化和/或髓鞘标记蛋白的表达或磷酸化水平增加,这表明ACE2在形态分化中起负作用。值得注意的是,ACE2的细胞内区域优先与活性GTP结合形式的Ras相互作用。因此,在亲和沉淀试验中,ACE2的敲低相对增加了GTP结合的Ras。实际上,抑制Ras会导致形态分化以及标记蛋白的表达或磷酸化水平降低,证实了Ras在分化中的正作用。这些结果表明ACE2本身作为少突胶质细胞形态分化的负调节因子的作用,新将ACE2添加到少突胶质细胞形态发生调节因子以及Ras结合蛋白列表中。这些发现可能有助于我们理解为什么SARS-CoV-2会在CNS中引起病理效应。