SUN1通过调节α-tubulin和CD36的表达,抑制人脂肪来源干细胞的成骨和促进其脂肪生成。

IF 5.3
Tingyu Fan, Jinhui Zhu, Wenqing Liu, Rongmei Qu, Asmat Ullah Khan, Yulian Shi, Jiaxuan Liu, Zhitao Zhou, Chujiang Xu, Jingxing Dai, Jun Ouyang
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引用次数: 0

摘要

Sad and UNC84 domain 1(SUN1)是一种核包膜蛋白,参与细胞过程,包括核运动和减数分裂。SUN1 在人类脂肪源性干细胞(hASCs)分化过程中发挥着引人关注的作用,但这一作用在很大程度上仍未确定。本研究旨在探讨 SUN1 在 hASCs 分化中的作用及其内在机制。利用 siRNAs,我们选择性地下调了 SUN1 和 CD36 的表达。使用nocodazole解聚微管,使用罗格列酮激活PPARγ。用 Western 印迹法定量检测 SUN1、PPARγ、α-微管蛋白、CD36、OPN 和脂肪连素蛋白的表达水平。碱性磷酸酶和油红 O 染色分别用于评估骨生成和脂肪生成。下调的SUN1表达增加了hASCs的骨生成,减少了脂肪生成,同时α-微管蛋白表达上调,CD36表达下调,PPARγ的核定位减少。微管解聚增加了 CD36 的表达。拯救实验表明,微管解聚抵消了下调的 SUN1 诱导的表型变化。本研究表明,SUN1 会影响 hASCs 向成骨和成脂系分化,表明其在细胞命运中的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SUN1 inhibits osteogenesis and promotes adipogenesis of human adipose-derived stem cells by regulating α-tubulin and CD36 expression

Sad and UNC84 domain 1 (SUN1) is a kind of nuclear envelope protein with established involvement in cellular processes, including nuclear motility and meiosis. SUN1 plays an intriguing role in human adipose-derived stem cells (hASCs) differentiation; however, this role remains largely undefined. This study was undertaken to investigate the role of SUN1 in hASCs differentiation, as well as its underlying mechanisms. Employing siRNAs, we selectively downregulated SUN1 and CD36 expression. Microtubules were depolymerized using nocodazole, and PPARγ was activated using rosiglitazone. Western blotting was performed to quantify SUN1, PPARγ, α-tubulin, CD36, OPN, and adiponectin protein expression levels. Alkaline phosphatase and Oil red O staining were used to assess osteogenesis and adipogenesis, respectively. Downregulated SUN1 expression increased osteogenesis and decreased adipogenesis in hASCs, concomitant with upregulated α-tubulin expression and downregulated CD36 expression, alongside reduced nuclear localization of PPARγ. Microtubule depolymerization increased CD36 expression. Rescue experiments indicated that microtubule depolymerization counteracted the downregulated SUN1-induced phenotypic changes. This study demonstrates that SUN1 influences the differentiation of hASCs towards osteogenic and adipogenic lineages, indicating its essential role in cell fate.

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来源期刊
CiteScore
11.50
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0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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