Bogle Rachael, Patrick Matthew T, Sreeskandarajan Sutharzan, Gharaee-Kermani Mehrnaz, Zhang Haihan, Li Qinmengge, Zhou Ruiwen, Ma Feiyang, Kahlenberg J Michelle, Plazyo Olesya, Elder James T, Billi Allison C, Gudjonsson Johann E, Tsoi Lam C
Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
J Invest Dermatol. 2025 May;145(5):1060-1069.e7. doi: 10.1016/j.jid.2024.09.010. Epub 2024 Sep 27.
The expressions of long noncoding RNAs (lncRNAs) and their roles in epidermal differentiation have been previously defined using bulk RNA sequencing. Despite their tissue-specific expression profiles, most lncRNAs are not well-annotated at the single-cell level. In this study, we evaluated the use of single-cell RNA sequencing to profile and characterize lncRNAs using data from 6 patients with psoriasis with paired uninvolved and lesional psoriatic skin. Despite their overall lower expression, we were able to detect >7000 skin-expressing lncRNAs and their cellular sources. Differential gene expression analysis revealed 137 differentially expressed lncRNAs in lesional psoriasis skin and identified 169 cell-type-specific lncRNAs. Keratinocytes had the highest number of differentially expressed lncRNA in psoriatic skin, which we validated using spatial transcriptomic data. We further showed that expression of the keratinocyte-specific lncRNA, AC020916.1, upregulated in lesional skin, is significantly correlated with expressions of genes participating in cell proliferation/epidermal differentiation, including SPRR2E and transcription factor ZFP36, particularly in the psoriatic skin. Our study highlights the potential for using single-cell RNA sequencing to profile skin-expressing lncRNA transcripts and to infer their cellular origins, providing a crucial approach that can be applied to the study of other inflammatory skin conditions.
长链非编码RNA(lncRNAs)的表达及其在表皮分化中的作用此前已通过批量RNA测序得以确定。尽管它们具有组织特异性表达谱,但大多数lncRNAs在单细胞水平上的注释并不完善。在本研究中,我们利用6例银屑病患者配对的非病变和病变银屑病皮肤的数据,评估了单细胞RNA测序用于分析和表征lncRNAs的效用。尽管它们的整体表达水平较低,但我们仍能够检测到7000多种在皮肤中表达的lncRNAs及其细胞来源。差异基因表达分析揭示了病变银屑病皮肤中有137种差异表达的lncRNAs,并鉴定出169种细胞类型特异性lncRNAs。角质形成细胞在银屑病皮肤中差异表达的lncRNA数量最多,我们使用空间转录组数据对其进行了验证。我们进一步表明,在病变皮肤中上调的角质形成细胞特异性lncRNA AC020916.1的表达与参与细胞增殖/表皮分化的基因(包括SPRR2E和转录因子ZFP36)的表达显著相关,尤其是在银屑病皮肤中。我们的研究突出了利用单细胞RNA测序分析皮肤表达的lncRNA转录本并推断其细胞来源的潜力,提供了一种可应用于其他炎症性皮肤病研究的关键方法。