Single-Cell RNA-Seq Identifies Dynamic Cardiac Transition Program from ADCs Induced by Leukemia Inhibitory Factor.
Jiayi YaoFeiyang MaLi ZhangChing ZhuMedet JumabayZehao YaoLumin WangXinjiang CaiDaoqin ZhangXiaojing QiaoKalyanam ShivkumarMatteo PellegriniYucheng YaoXiuju WuKristina I BöstromPublished in: Stem cells (Dayton, Ohio) (2022)
Adipose-derived cells (ADCs) from white adipose tissue are promising stem cell candidates because of their large regenerative reserves and the potential for cardiac regeneration. However, given the heterogeneity of ADC and its unsolved mechanisms of cardiac acquisition, ADC-cardiac transition efficiency remains low. In this study, we explored the heterogeneity of ADCs and the cellular kinetics of 39,432 single-cell transcriptomes along the leukemia inhibitory factor (LIF)-induced ADC-cardiac transition. We identified distinct ADC subpopulations that reacted differentially to LIF when entering the cardiomyogenic program, further demonstrating that ADC-myogenesis is time-dependent and initiates from transient changes in nuclear factor erythroid 2-related factor 2 (Nrf2) signaling. At later stages, pseudotime analysis of ADCs navigated a trajectory with 2 branches corresponding to activated myofibroblast or cardiomyocyte-like cells. Our findings offer a high-resolution dissection of ADC heterogeneity and cell fate during ADC-cardiac transition, thus providing new insights into potential cardiac stem cells.
Keyphrases
- single cell
- stem cells
- rna seq
- left ventricular
- diffusion weighted imaging
- diffusion weighted
- adipose tissue
- high resolution
- high throughput
- oxidative stress
- acute myeloid leukemia
- bone marrow
- magnetic resonance
- type diabetes
- quality improvement
- heart failure
- genome wide
- mesenchymal stem cells
- induced apoptosis
- insulin resistance
- magnetic resonance imaging
- risk assessment
- mass spectrometry
- endothelial cells
- computed tomography
- cell fate
- signaling pathway
- diabetic rats
- cell therapy
- drug induced
- atrial fibrillation
- inflammatory response
- high glucose