Li Yong, Qian Yisong, Huang Evan, Schwarz Zain, Tai Hannah, Tillock Katherine, Lei Tianhua, Yang Xiaofeng, Fu Mingui
Department of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA; Department of Anesthesiology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330006, China.
Key Lab for Arteriosclerology of Hunan Province, International Joint Laboratory for Arteriosclerotic Disease Research of Hunan Province, Institute of Cardiovascular Disease, University of South China, Hengyang 421001, China.
Biochim Biophys Acta Mol Cell Res. 2025 Jul 1;1872(7):120017. doi: 10.1016/j.bbamcr.2025.120017.
It was recently reported that RNAs can be glycosylated, and such glycosylated RNAs (referred to as glycoRNAs) are located on the outer cell surface. We here reported that there are two forms of glycoRNAs, named as glycoRNA-L and glycoRNA-S, robustly expressed in human monocytes. We verified that the glycoRNA-S specifically detected in human monocytes is synthesized by enzyme-catalyzed conjugation, but not artificial products of labelling probe. RNase-treatment removed both glycoRNA-L and glycoRNA-S, suggesting that they are localized on cell surface. Removing glycoRNAs significantly suppressed the interaction of human monocytes with endothelial cells, suggesting that glycoRNAs mediate human monocyte adhesion. Using flow cytometry, immunoprecipitation and northern blotting we identified Siglec-5 as the binding receptor of glycoRNAs. Siglec-5 is expressed in human endothelial cells but presented on endothelial cell surface when endothelial cells are activated. We observed that glycoRNA-L was heavily labeled with sialic acid, whereas glycoRNA-S was heavily labeled with N-acetylgalactosamine and N-acetylglucosamine. Together, these results demonstrate that two forms of glycoRNAs exist in human monocytes, which may play significant role in controlling the interaction of human monocytes and endothelial cells and contribute to the pathogenesis of inflammatory diseases.
最近有报道称RNA可以被糖基化,这种糖基化的RNA(称为糖基化RNA,即glycoRNAs)位于细胞外表面。我们在此报道,在人类单核细胞中强烈表达的糖基化RNA有两种形式,分别命名为glycoRNA-L和glycoRNA-S。我们证实,在人类单核细胞中特异性检测到的glycoRNA-S是通过酶催化结合合成的,而不是标记探针的人工产物。核糖核酸酶处理可去除glycoRNA-L和glycoRNA-S,这表明它们定位于细胞表面。去除糖基化RNA显著抑制了人类单核细胞与内皮细胞的相互作用,这表明糖基化RNA介导了人类单核细胞的黏附。通过流式细胞术、免疫沉淀和Northern印迹法,我们鉴定出唾液酸结合免疫球蛋白样凝集素5(Siglec-5)是糖基化RNA的结合受体。Siglec-5在人类内皮细胞中表达,但在内皮细胞被激活时呈现在内皮细胞表面。我们观察到,glycoRNA-L被唾液酸大量标记,而glycoRNA-S被N-乙酰半乳糖胺和N-乙酰葡糖胺大量标记。总之,这些结果表明人类单核细胞中存在两种形式的糖基化RNA,它们可能在控制人类单核细胞与内皮细胞的相互作用中发挥重要作用,并有助于炎症性疾病的发病机制。