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间充质干细胞来源的神经祖细胞通过旁分泌机制减弱促炎性小胶质细胞的激活。

Mesenchymal stem cell-derived neural progenitors attenuate proinflammatory microglial activation via paracrine mechanisms.

作者信息

Harris Violaine K, Bishop Derek, Wollowitz Jaina, Carling Gillian, Carlson Alyssa L, Daviaud Nicolas, Sadiq Saud A

机构信息

Tisch Multiple Sclerosis Research Center of New York, NY 10019, USA.

出版信息

Regen Med. 2023 Mar;18(3):259-273. doi: 10.2217/rme-2023-0005. Epub 2023 Feb 27.

Abstract

Mesenchymal stem cell-derived neural progenitor cell (MSC-NP) therapy is an experimental approach to treat multiple sclerosis. The influence of MSC-NPs on microglial activation was investigated. Microglia were stimulated in the presence of MSC-NP-conditioned media, and proinflammatory or proregenerative marker expression was assessed by quantitative PCR and ELISA. Microglia stimulated in the presence of MSC-NP-conditioned media displayed reduced expression of proinflammatory markers including CCL2, increased expression of proregenerative markers and reduced phagocytic activity. The paracrine effects of MSC-NPs from multiple donors correlated with gene expression and was reversed by TGF-β signaling inhibition. MSC-NPs promote beneficial microglial polarization through secreted factors. This study suggests that microglia are a potential therapeutic target of MSC-NP cell therapy.

摘要

间充质干细胞衍生的神经祖细胞(MSC-NP)疗法是一种治疗多发性硬化症的实验方法。研究了MSC-NP对小胶质细胞激活的影响。在MSC-NP条件培养基存在下刺激小胶质细胞,并通过定量PCR和ELISA评估促炎或促再生标志物的表达。在MSC-NP条件培养基存在下刺激的小胶质细胞显示促炎标志物(包括CCL2)的表达降低,促再生标志物的表达增加,吞噬活性降低。来自多个供体的MSC-NP的旁分泌作用与基因表达相关,并通过TGF-β信号抑制而逆转。MSC-NP通过分泌因子促进有益的小胶质细胞极化。这项研究表明,小胶质细胞是MSC-NP细胞疗法的潜在治疗靶点。

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