Liu Chang, Zhang Yanli, Ma Zhanchuan, Yi Huanfa
Central Laboratory, The First Hospital of Jilin University, Changchun, China.
Key Laboratory of Organ Regeneration and Transplantation, Ministry of Education, Changchun, China.
Front Cell Dev Biol. 2022 Jun 20;10:831215. doi: 10.3389/fcell.2022.831215. eCollection 2022.
CD4 T cells differentiate towards different subpopulations through the regulation of lineage-specific cytokines and transcription factors, which flexibly respond to various immune challenges. However, considerable work has demonstrated that the CD4 T-cell differentiation mechanism is complex and not limited to transcription factors and cytokines. Long noncoding RNAs (lncRNAs) are RNA molecules with lengths exceeding 200 base pairs that regulate various biological processes and genes. LncRNAs have been found to conciliate the plasticity of CD4 T-cell differentiation. Then, we focused on lncRNAs involved in CD4 T-cell differentiation and enlisted some molecular thought into the plasticity and functional heterogeneity of CD4 T cells. Furthermore, elucidating how lncRNAs modulate CD4 T-cell differentiation in disparate immune diseases may provide a basis for the pathological mechanism of immune-mediated diseases.
CD4 T细胞通过谱系特异性细胞因子和转录因子的调控向不同亚群分化,这些因子能灵活应对各种免疫挑战。然而,大量研究表明,CD4 T细胞分化机制复杂,并不局限于转录因子和细胞因子。长链非编码RNA(lncRNAs)是长度超过200个碱基对的RNA分子,可调控各种生物学过程和基因。已发现lncRNAs可调节CD4 T细胞分化的可塑性。随后,我们聚焦于参与CD4 T细胞分化的lncRNAs,并对CD4 T细胞的可塑性和功能异质性提出了一些分子层面的见解。此外,阐明lncRNAs如何在不同免疫疾病中调节CD4 T细胞分化,可能为免疫介导疾病的病理机制提供依据。