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脐带和骨髓来源的间充质干细胞在脂肪细胞分化过程中初级纤毛形成和伸长的不同时间动态。

Different temporal dynamics of primary cilia formation and elongation during adipocyte differentiation in umbilical cord- and bone marrow-derived mesenchymal stem cells.

作者信息

Hirai Masako, Inoue Naokazu, Nagai Tomoaki, Nishita Michiru

机构信息

Department of Biochemistry, Fukushima Medical University School of Medicine, Fukushima, 960-1295, Japan.

Department of Cell Science, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, 960-1295, Fukushima, Japan.

出版信息

Biochem Biophys Res Commun. 2025 Jul 1;768:151918. doi: 10.1016/j.bbrc.2025.151918. Epub 2025 Apr 28.

Abstract

Umbilical cord-derived mesenchymal stem cells (UC-MSCs) are considered a promising alternative to bone marrow-derived MSCs (BM-MSCs) due to their high proliferative capacity and non-invasive accessibility. While UC-MSCs exhibit osteogenic, chondrogenic, and myogenic differentiation potential comparable to BM-MSCs, their adipogenic differentiation is significantly delayed. To investigate the underlying mechanisms, we focused on primary cilia, sensory organelles that regulate key adipogenic signaling pathways, including the insulin-Akt axis. Under serum-starved, growth-arrest conditions, both UC-MSCs and BM-MSCs formed primary cilia at similar frequencies and lengths; however, under serum-fed, proliferative conditions, UC-MSCs showed a significantly lower frequency of ciliation. During adipogenesis, BM-MSCs exhibited early ciliogenesis and stable cilium length, whereas UC-MSCs displayed delayed ciliogenesis and developed significantly longer cilia after repeated induction cycles. Despite comparable ciliation frequency and longer cilia in UC-MSCs at later stages, insulin-induced Akt activation was reduced compared to BM-MSCs, suggesting that primary cilia in UC-MSCs may be less efficient in sensing insulin. These alterations in insulin signaling may contribute to the reduced adipogenic capacity observed in UC-MSCs.

摘要

脐带间充质干细胞(UC-MSCs)因其高增殖能力和非侵入性获取方式,被认为是骨髓间充质干细胞(BM-MSCs)的一种有前景的替代物。虽然UC-MSCs表现出与BM-MSCs相当的成骨、成软骨和成肌分化潜能,但其脂肪生成分化明显延迟。为了研究潜在机制,我们聚焦于初级纤毛,这是调节关键脂肪生成信号通路(包括胰岛素-Akt轴)的感觉细胞器。在血清饥饿、生长停滞条件下,UC-MSCs和BM-MSCs以相似的频率和长度形成初级纤毛;然而,在血清喂养、增殖条件下,UC-MSCs的纤毛形成频率显著降低。在脂肪生成过程中,BM-MSCs表现出早期纤毛发生和稳定的纤毛长度,而UC-MSCs则表现出延迟的纤毛发生,并且在重复诱导周期后形成明显更长的纤毛。尽管在后期UC-MSCs的纤毛形成频率相当且纤毛更长,但与BM-MSCs相比,胰岛素诱导的Akt激活减少,这表明UC-MSCs中的初级纤毛在感知胰岛素方面可能效率较低。胰岛素信号的这些改变可能导致UC-MSCs中观察到的脂肪生成能力降低。

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