Yap/Taz 活性与支持肌母细胞增殖的磷酸甘油酸脱氢酶的表达增加有关。

IF 3.2 3区 生物学 Q3 CELL BIOLOGY Cell and Tissue Research Pub Date : 2024-03-01 Epub Date: 2024-01-06 DOI:10.1007/s00441-023-03851-w
Marius Meinhold, Sander Verbrugge, Andi Shi, Martin Schönfelder, Lore Becker, Richard T Jaspers, Peter S Zammit, Henning Wackerhage
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引用次数: 0

摘要

在骨骼肌中,Hippo效应子Yap能促进卫星细胞、肌母细胞和横纹肌母细胞的增殖,但却能阻止肌原纤维分化成多核肌纤维。我们以前注意到,Yap 驱动丝氨酸生物合成途径的第一个酶--磷酸甘油酸脱氢酶(Phgdh)的表达。在这里,我们研究了卫星细胞和肌母细胞中 Phgdh 的调控和功能,发现卫星细胞活化过程中 Phgdh 蛋白增加。对已发表数据的分析表明,小鼠胫骨前肌的 Phgdh mRNA 在注射心脏毒素后再生的第 3 天和增效剂损伤肌肉的第一周高度表达,而此时增殖标记物也大量表达。最后,siRNA 介导的 PHGDH 敲除可显著减少成肌细胞数量和增殖率。总之,我们的数据表明,Phgdh 是一种促进增殖的代谢酶,当静止卫星细胞被激活时会被诱导。
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Yap/Taz activity is associated with increased expression of phosphoglycerate dehydrogenase that supports myoblast proliferation.

In skeletal muscle, the Hippo effector Yap promotes satellite cell, myoblast, and rhabdomyoblast proliferation but prevents myogenic differentiation into multinucleated muscle fibres. We previously noted that Yap drives expression of the first enzyme of the serine biosynthesis pathway, phosphoglycerate dehydrogenase (Phgdh). Here, we examined the regulation and function of Phgdh in satellite cells and myoblasts and found that Phgdh protein increased during satellite cell activation. Analysis of published data reveal that Phgdh mRNA in mouse tibialis anterior muscle was highly expressed at day 3 of regeneration after cardiotoxin injection, when markers of proliferation are also robustly expressed and in the first week of synergist-ablated muscle. Finally, siRNA-mediated knockdown of PHGDH significantly reduced myoblast numbers and the proliferation rate. Collectively, our data suggest that Phgdh is a proliferation-enhancing metabolic enzyme that is induced when quiescent satellite cells become activated.

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来源期刊
Cell and Tissue Research
Cell and Tissue Research 生物-细胞生物学
CiteScore
7.00
自引率
2.80%
发文量
142
审稿时长
1 months
期刊介绍: The journal publishes regular articles and reviews in the areas of molecular, cell, and supracellular biology. In particular, the journal intends to provide a forum for publishing data that analyze the supracellular, integrative actions of gene products and their impact on the formation of tissue structure and function. Submission of papers with an emphasis on structure-function relationships as revealed by recombinant molecular technologies is especially encouraged. Areas of research with a long-standing tradition of publishing in Cell & Tissue Research include: - neurobiology - neuroendocrinology - endocrinology - reproductive biology - skeletal and immune systems - development - stem cells - muscle biology.
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