Direct Conversion of Human Fibroblasts into Adipocytes Using a Novel Small Molecular Compound: Implications for Regenerative Therapy for Adipose Tissue Defects.
Yoshihiro SowaTsunao KishidaFiona LouisSeiji SawaiMakoto SekiToshiaki NumajiriKenji TakahashiOsam MazdaPublished in: Cells (2021)
There is a need in plastic surgery to prepare autologous adipocytes that can be transplanted in patients to reconstruct soft tissue defects caused by tumor resection, including breast cancer, and by trauma and other diseases. Direct conversion of somatic cells into adipocytes may allow sufficient functional adipocytes to be obtained for use in regeneration therapy. Chemical libraries of 10,800 molecules were screened for the ability to induce lipid accumulation in human dermal fibroblasts (HDFs) in culture. Chemical compound-mediated directly converted adipocytes (CCCAs) were characterized by lipid staining, immunostaining, and qRT-PCR, and were also tested for adipokine secretion and glucose uptake. CCCAs were also implanted into mice to examine their distribution in vivo. STK287794 was identified as a small molecule that induced the accumulation of lipid droplets in HDFs. CCCAs expressed adipocyte-related genes, secreted adiponectin and leptin, and abundantly incorporated glucose. After implantation in mice, CCCAs resided in granulation tissue and remained adipose-like. HDFs were successfully converted into adipocytes by adding a single chemical compound, STK287794. C/EBPα and PPARγ were upregulated in STK287794-treated cells, which strongly suggests involvement of these adipocyte-related transcription factors in the chemical direct conversion. Our method may be useful for the preparation of autogenous adipocytes for transplantation therapy for soft tissue defects and fat tissue atrophy.
Keyphrases
- adipose tissue
- insulin resistance
- high fat diet induced
- high fat diet
- soft tissue
- small molecule
- induced apoptosis
- stem cells
- endothelial cells
- cell therapy
- cell cycle arrest
- newly diagnosed
- mesenchymal stem cells
- transcription factor
- fatty acid
- type diabetes
- end stage renal disease
- metabolic syndrome
- high glucose
- chronic kidney disease
- extracellular matrix
- induced pluripotent stem cells
- skeletal muscle
- oxidative stress
- gene expression
- high resolution
- cell proliferation
- diabetic rats
- single molecule
- solid phase extraction
- pluripotent stem cells
- genome wide
- endoplasmic reticulum stress
- molecularly imprinted