
AbstractBoth brown adipocytes (BAC) and beige cells hold therapeutic potential for the treatment of metabolic disorders. Unfortunately, the amount and activity of these cells are limited in adults. Although BAC marker expression has been shown in peri-renal adipose tissues in children and adults, functional assessment is lacking. Furthermore, it is entirely unknown whether adipose progenitors are present in human embryo and able to give rise to BAC in situ during evolution. Therefore, adipose tissues in the interscapular and peri-renal regions were dissected from human embryo and subcutaneous white adipose tissues (sWAT) were obtained from an adult. After subjected to differentiation in vitro, adipocyte progenitors were detected present in all these adipose tissues. When stimulated for adipogenesis, differentiated adipocytes in the intercapular and peri-renal regions showed similar features: (1) induced BAC and beige cell marker expression including UCP1 and PRDM16 and comparable mitochondrion copy number; (2) similar gene expression patterns by RNA-Seq analysis; and (3) similar maximal oxygen consumption rates examined by respirometry. Nevertheless, stimulation of adipocyte progenitors in sWAT induces neither BAC and beige cell marker expression nor any change of oxygen consumption. In conclusion, peri-renal adipocyte progenitors in human embryo hold browning potential for BAC production.
Adipogenesis, Sequence Analysis, RNA, Stem Cells, Adipocytes, White, Membrane Proteins, Embryo, Mammalian, Article, Mitochondria, DNA-Binding Proteins, Tumor Necrosis Factor Receptor Superfamily, Member 9, Adipocytes, Brown, Humans, RNA, T-Box Domain Proteins, Transcriptome, Cells, Cultured, Uncoupling Protein 1, Transcription Factors
Adipogenesis, Sequence Analysis, RNA, Stem Cells, Adipocytes, White, Membrane Proteins, Embryo, Mammalian, Article, Mitochondria, DNA-Binding Proteins, Tumor Necrosis Factor Receptor Superfamily, Member 9, Adipocytes, Brown, Humans, RNA, T-Box Domain Proteins, Transcriptome, Cells, Cultured, Uncoupling Protein 1, Transcription Factors
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