Goethe University Frankfurt, Institute for Cardiovascular Physiology, Frankfurt, Germany.
German Center of Cardiovascular Research (DZHK), Partner site RheinMain, Frankfurt, Germany.
Commun Biol. 2024 Sep 13;7(1):1131. doi: 10.1038/s42003-024-06794-2.
Monocytes, the circulating macrophage precursors, contribute to diseases like atherosclerosis and asthma. Long non-coding RNAs (lncRNAs) have been shown to modulate the phenotype and inflammatory capacity of monocytes. We previously discovered the lncRNA SMANTIS, which contributes to cellular phenotype expression by controlling BRG1 in mesenchymal cells. Here, we report that SMANTIS is particularly highly expressed in monocytes and lost during differentiation into macrophages. Moreover, different types of myeloid leukemia presented specific SMANTIS expression patterns. Interaction studies revealed that SMANTIS binds RUNX1, a transcription factor frequently mutated in AML, primarily through its Alu-element on the RUNT domain. RNA-seq after CRISPR/Cas9-mediated deletion of SMANTIS or RUNX1 revealed an association with cell adhesion and both limited the monocyte adhesion to endothelial cells. Mechanistically, SMANTIS KO reduced RUNX1 genomic binding and altered the interaction of RUNX1 with EP300 and CBFB. Collectively, SMANTIS interacts with RUNX1 and attenuates monocyte adhesion, which might limit monocyte vascular egress.
单核细胞是循环中的巨噬细胞前体,可导致动脉粥样硬化和哮喘等疾病。长链非编码 RNA(lncRNA)已被证明可调节单核细胞的表型和炎症能力。我们之前发现了 lncRNA SMANTIS,它通过控制间充质细胞中的 BRG1 来促进细胞表型表达。在这里,我们报告称 SMANTIS 在单核细胞中表达特别高,并在分化为巨噬细胞的过程中丢失。此外,不同类型的髓性白血病呈现出特定的 SMANTIS 表达模式。相互作用研究表明,SMANTIS 与 RUNX1 结合,RUNX1 是 AML 中经常发生突变的转录因子,主要通过其 RUNT 结构域上的 Alu 元件结合。SMANTIS 或 RUNX1 的 CRISPR/Cas9 介导缺失后的 RNA-seq 显示与细胞黏附有关,两者均限制单核细胞黏附到内皮细胞上。从机制上讲,SMANTIS KO 降低了 RUNX1 的基因组结合,并改变了 RUNX1 与 EP300 和 CBFB 的相互作用。总之,SMANTIS 与 RUNX1 相互作用,减弱单核细胞黏附,从而可能限制单核细胞血管迁出。