PSME4通过YAP1降解决定间充质干细胞走向心脏承诺的命运。

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Mira Kim, Yong Sook Kim, Youngkeun Ahn, Gwang Hyeon Eom, Somy Yoon
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引用次数: 0

摘要

急性循环事件后心肌的再生仍然是一个挑战,尽管许多努力。间充质干细胞(MSCs)是一种很有前途的细胞治疗选择,但将其分化为心肌细胞是一个耗时的过程。虽然已经证明PSME4可以降解乙酰yap1,但PSME4在MSCs心脏承诺中的作用尚未完全阐明。在这里,我们报道了PSME4在MSCs心脏承诺中的新作用。研究发现,在原代培养的小鼠间充质干细胞中使用apicidin过夜可导致快速的心脏承诺,而来自PSME4敲除小鼠的间充质干细胞则不会经历这一过程。在永活的人间充质干细胞中,还使用慢病毒介导的PSME4敲低观察到心脏承诺。免疫荧光和Western blot实验显示,即使在apicidin处理后,YAP1仍存在于PSME4敲除细胞的细胞核中。为了研究YAP1去除的重要性,我们同时用shYAP1和apicidin处理MSCs。这种联合治疗导致快速消除YAP1和加速心脏承诺。然而,在apicidin处理的MSCs中,乙酰化抗性YAP1的过度表达阻碍了心脏承诺。除apicidin外,利用tubastatin A和HDAC6 siRNA证实了组蛋白去乙酰化酶(HDAC)抑制对心脏承诺的普遍作用。总的来说,本研究表明PSME4对于促进MSCs的心脏承诺至关重要。HDAC抑制使YAP1乙酰化并促进其转运到细胞核,在那里它被PSME4移除,促进心脏承诺。YAP1在细胞核中移位或被清除的失败导致MSCs无法进行心脏承托。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

PSME4 determines mesenchymal stem cell fate towards cardiac commitment through YAP1 degradation.

PSME4 determines mesenchymal stem cell fate towards cardiac commitment through YAP1 degradation.

PSME4 determines mesenchymal stem cell fate towards cardiac commitment through YAP1 degradation.

PSME4 determines mesenchymal stem cell fate towards cardiac commitment through YAP1 degradation.

The regeneration of myocardium following acute circulatory events remains a challenge, despite numerous efforts. Mesenchymal stem cells (MSCs) present a promising cell therapy option, but their differentiation into cardiomyocytes is a time-consuming process. Although it has been demonstrated that PSME4 degrades acetyl-YAP1, the role of PSME4 in the cardiac commitment of MSCs has not been fully elucidated. Here we reported the novel role of PSME4 in MSCs cardiac commitment. It was found that overnight treatment with apicidin in primary-cultured mouse MSCs led to rapid cardiac commitment, while MSCs from PSME4 knock-out mice did not undergo this process. Cardiac commitment was also observed using lentivirus-mediated PSME4 knockdown in immortalized human MSCs. Immunofluorescence and Western blot experiments revealed that YAP1 persisted in the nucleus of PSME4 knockdown cells even after apicidin treatment. To investigate the importance of YAP1 removal, MSCs were treated with shYAP1 and apicidin simultaneously. This combined treatment resulted in rapid YAP1 elimination and accelerated cardiac commitment. However, overexpression of acetylation-resistant YAP1 in apicidin-treated MSCs impeded cardiac commitment. In addition to apicidin, the universal effect of histone deacetylase (HDAC) inhibition on cardiac commitment was confirmed using tubastatin A and HDAC6 siRNA. Collectively, this study demonstrates that PSME4 is crucial for promoting the cardiac commitment of MSCs. HDAC inhibition acetylates YAP1 and facilitates its translocation to the nucleus, where it is removed by PSME4, promoting cardiac commitment. The failure of YAP1 to translocate or be eliminated from the nucleus results in the MSCs' inability to undergo cardiac commitment.

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来源期刊
Korean Journal of Physiology & Pharmacology
Korean Journal of Physiology & Pharmacology PHARMACOLOGY & PHARMACY-PHYSIOLOGY
CiteScore
3.20
自引率
5.00%
发文量
53
审稿时长
6-12 weeks
期刊介绍: The Korean Journal of Physiology & Pharmacology (Korean J. Physiol. Pharmacol., KJPP) is the official journal of both the Korean Physiological Society (KPS) and the Korean Society of Pharmacology (KSP). The journal launched in 1997 and is published bi-monthly in English. KJPP publishes original, peer-reviewed, scientific research-based articles that report successful advances in physiology and pharmacology. KJPP welcomes the submission of all original research articles in the field of physiology and pharmacology, especially the new and innovative findings. The scope of researches includes the action mechanism, pharmacological effect, utilization, and interaction of chemicals with biological system as well as the development of new drug targets. Theoretical articles that use computational models for further understanding of the physiological or pharmacological processes are also welcomed. Investigative translational research articles on human disease with an emphasis on physiology or pharmacology are also invited. KJPP does not publish work on the actions of crude biological extracts of either unknown chemical composition (e.g. unpurified and unvalidated) or unknown concentration. Reviews are normally commissioned, but consideration will be given to unsolicited contributions. All papers accepted for publication in KJPP will appear simultaneously in the printed Journal and online.
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