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DOI 10.1016/j.niox.2024.02.004

Медицинская библиотека · Nitric oxide : biology and chemistry · 2024

Protein S-nitrosylation is involved in valproic acid-promoted neuronal differentiation of adipose tissue-derived stem cells.

Kurokawa Kenta, Sogawa Kazuyuki, Suzuki Takehito, Miyazaki Yoko, Tanaka Kazuaki, Usami Makoto, Takizawa Tatsuya

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Neuronal differentiation of adipose tissue-derived stem cells (ASCs) is greatly promoted by valproic acid (VPA) with cAMP elevating agents thorough NO signaling pathways, but its mechanism is not fully understood. In the present study, we investigate the involvement of protein S-nitrosylation in the VPA-promoted neuronal differentiation of ASCs. The whole amount of S-nitrosylated protein was increased by the treatment with VPA alone for three days in ASCs. An inhibitor of thioredoxin reductase (TrxR), auranofin, further increased the amount of S-nitrosylated protein and enhances the VPA-promoted neuronal differentiation in ASCs. On the contrary, another inhibitor of TrxR, dinitrochlorobenzene, inhibited the VPA-promoted neuronal differentiation in ASCs even with cAMP elevating agents, which was accompanied by unexpectedly decreased S-nitrosylated protein. It was considered from these results that increased protein S-nitrosylation is involved in VPA-promoted neuronal differentiation of ASCs. By the proteomic analysis of S-nitrosylated protein in VPA-treated ASCs, no identified proteins could be specifically related to VPA-promoted neuronal differentiation. The identified proteins, however, included those involved in the metabolism of substances regulating neuronal differentiation, such as aspartate and glutamate.

Для цитирования: Kurokawa Kenta, Sogawa Kazuyuki, Suzuki Takehito, Miyazaki Yoko, Tanaka Kazuaki, Usami Makoto, Takizawa Tatsuya. Protein S-nitrosylation is involved in valproic acid-promoted neuronal differentiation of adipose tissue-derived stem cells.. Nitric oxide : biology and chemistry. 2024. DOI: 10.1016/j.niox.2024.02.004.

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