Transcriptional determinants of lipid mobilization in human adipocytes.
Alison C LudzkiMattias HansenDanae ZareifiJutta JalkanenZhiqiang HuangMuhmmad Omar-HmeadiGianluca RenziFelix KlingelhuberSebastian BolandYohannes A AmbawNa WangAnastasios DamdimopoulosJianping LiuTomas JernbergPaul PetrusPeter ArnerNatalie KrahmerRongrong FanEckardt TreuterHui GaoMikael RydénNiklas MejhertPublished in: Science advances (2024)
Defects in adipocyte lipolysis drive multiple aspects of cardiometabolic disease, but the transcriptional framework controlling this process has not been established. To address this, we performed a targeted perturbation screen in primary human adipocytes. Our analyses identified 37 transcriptional regulators of lipid mobilization, which we classified as (i) transcription factors, (ii) histone chaperones, and (iii) mRNA processing proteins. On the basis of its strong relationship with multiple readouts of lipolysis in patient samples, we performed mechanistic studies on one hit, ZNF189 , which encodes the zinc finger protein 189. Using mass spectrometry and chromatin profiling techniques, we show that ZNF189 interacts with the tripartite motif family member TRIM28 and represses the transcription of an adipocyte-specific isoform of phosphodiesterase 1B (PDE1B2). The regulation of lipid mobilization by ZNF189 requires PDE1B2, and the overexpression of PDE1B2 is sufficient to attenuate hormone-stimulated lipolysis. Thus, our work identifies the ZNF189-PDE1B2 axis as a determinant of human adipocyte lipolysis and highlights a link between chromatin architecture and lipid mobilization.
Keyphrases
- adipose tissue
- transcription factor
- endothelial cells
- fatty acid
- insulin resistance
- gene expression
- mass spectrometry
- genome wide
- pluripotent stem cells
- induced pluripotent stem cells
- dna binding
- dna methylation
- cell proliferation
- dna damage
- binding protein
- type diabetes
- oxidative stress
- case report
- liquid chromatography
- cancer therapy
- skeletal muscle
- single cell
- drug delivery
- protein protein
- simultaneous determination