Wang Yuanxin, Dede Merve, Mohanty Vakul, Dou Jinzhuang, Li Ziyi, Chen Ken
Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Cell Rep Methods. 2024 Dec 16;4(12):100913. doi: 10.1016/j.crmeth.2024.100913. Epub 2024 Dec 6.
Decoding cellular state transitions is crucial for understanding complex biological processes in development and disease. While recent advancements in single-cell RNA sequencing (scRNA-seq) offer insights into cellular trajectories, existing tools primarily study expressional rather than regulatory state shifts. We present CellTran, a statistical approach utilizing paired-gene expression correlations to detect transition cells from scRNA-seq data without explicitly resolving gene regulatory networks. Applying our approach to various contexts, including tissue regeneration, embryonic development, preinvasive lesions, and humoral responses post-vaccination, reveals transition cells and their distinct gene expression profiles. Our study sheds light on the underlying molecular mechanisms driving cellular state transitions, enhancing our ability to identify therapeutic targets for disease interventions.
解码细胞状态转变对于理解发育和疾病中的复杂生物学过程至关重要。虽然单细胞RNA测序(scRNA-seq)的最新进展为细胞轨迹提供了见解,但现有工具主要研究表达状态而非调控状态的转变。我们提出了CellTran,这是一种统计方法,利用配对基因表达相关性从scRNA-seq数据中检测转变细胞,而无需明确解析基因调控网络。将我们的方法应用于各种情况,包括组织再生、胚胎发育、癌前病变和疫苗接种后的体液反应,揭示了转变细胞及其独特的基因表达谱。我们的研究揭示了驱动细胞状态转变的潜在分子机制,增强了我们识别疾病干预治疗靶点的能力。