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DOI 10.31083/j.fbl2903096

Медицинская библиотека · Frontiers in bioscience (Landmark edition) · 2024

Conditioned Media from Deer Antler Stem Cells Effectively Alleviate Type 1 Diabetes Mellitus Possibly via Inhibiting the NF-κB Signaling Pathway.

Wang Dongxu, Ren Jing, Li Jiping, Li Xiuying, Ying Jinchi, Jiang Tiantian, Wang Zhen, Pan Zheng, Guo Qianqian, Li Chunyi, Zhang Guokun

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Аннотация

BACKGROUND

Type 1 diabetes mellitus (T1D) represents a severe threat to human health. Persistent hyperglycemia and dyslipidemia can lead to damaged liver function, while effective interventions for these complications are currently lacking. Deer antler stem cells (AnSCs), a novel type of adult stem cells, significantly reduced liver injury, which was speculated to be achieved through the paracrine pathway.

METHODS

In this study, AnSC-conditioned medium (AnSC-CM) was used to treat C57BL/6 mice with T1D symptoms induced by streptozotocin (STZ). The therapeutic effects of AnSC-CM on T1D were evaluated, and the underlying mechanism was investigated.

RESULTS

It was shown that AnSC-CM alleviated the T1D symptom: decreased body weight, increased blood glucose levels and islet lesions, and reduced insulin secretion. Moreover, AnSC-CM treatment improved liver function and mitigated liver injury in T1D mice. Impressively, the therapeutic effects of AnSC-CM on T1D were better than those of bone marrow mesenchymal stem cell-CM (BMSC-CM). The mechanistic study revealed that AnSC-CM significantly downregulated the NF-κB signaling pathway in both pancreatic and liver tissues.

CONCLUSIONS

Therapeutic effects of AnSC-CM on STZ-induced T1D and liver injury may be achieved through targeting the NF-κB signaling pathway.

Для цитирования: Wang Dongxu, Ren Jing, Li Jiping, Li Xiuying, Ying Jinchi, Jiang Tiantian, Wang Zhen, Pan Zheng, Guo Qianqian, Li Chunyi, Zhang Guokun. Conditioned Media from Deer Antler Stem Cells Effectively Alleviate Type 1 Diabetes Mellitus Possibly via Inhibiting the NF-κB Signaling Pathway.. Frontiers in bioscience (Landmark edition). 2024. DOI: 10.31083/j.fbl2903096.

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