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SMOX and SMS Responsible for Polyamine Metabolism Enhanced Adipogenesis

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Abstract Adipose tissue regulating carbohydrate and lipid metabolism had been extensively focused. However, the regulation of amino acid metabolism during adipocyte differentiation remained detailed. Here we applied RNA-Seq technique to establish the transcriptional landscapes of amino acid metabolism during adipogenesis. We totally screened 17 differentially expressed genes (DEGs) for amino acid metabolism at 7, 14, 21, and 28 days during adipogenesis from human mesenchymal stem cells (hMSCs), especially with 13 up-regulated genes most prevalent in our adipogenic anecdote. Small molecule metabolic process was the most enriched biological process following by oxidation-reduction process. Interestingly, the enforced expression of SMOX (spermine oxidase) responsible for polyamine metabolism in arginine and proline metabolism pathway facilitated adipogenesis more than SMS (spermine synthase) using RNA interference (RNAi). The established potential regulatory network further suggested that adipocyte differentiation tightly related with the basal metabolism of amino acid metabolism with the partially confirmed SMS-SMOX-PPARG signaling pathway. It would highlight the effect of adipogenesis on amino acid metabolism in adipocyte biology and provide the potential treatment strategy for the study of fat metabolic diseases.
Title: SMOX and SMS Responsible for Polyamine Metabolism Enhanced Adipogenesis
Description:
Abstract Adipose tissue regulating carbohydrate and lipid metabolism had been extensively focused.
However, the regulation of amino acid metabolism during adipocyte differentiation remained detailed.
Here we applied RNA-Seq technique to establish the transcriptional landscapes of amino acid metabolism during adipogenesis.
We totally screened 17 differentially expressed genes (DEGs) for amino acid metabolism at 7, 14, 21, and 28 days during adipogenesis from human mesenchymal stem cells (hMSCs), especially with 13 up-regulated genes most prevalent in our adipogenic anecdote.
Small molecule metabolic process was the most enriched biological process following by oxidation-reduction process.
Interestingly, the enforced expression of SMOX (spermine oxidase) responsible for polyamine metabolism in arginine and proline metabolism pathway facilitated adipogenesis more than SMS (spermine synthase) using RNA interference (RNAi).
The established potential regulatory network further suggested that adipocyte differentiation tightly related with the basal metabolism of amino acid metabolism with the partially confirmed SMS-SMOX-PPARG signaling pathway.
It would highlight the effect of adipogenesis on amino acid metabolism in adipocyte biology and provide the potential treatment strategy for the study of fat metabolic diseases.

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