基于致死表型的数据库筛选确定神经酰胺是原始条纹形成的负调控因子。

IF 4 2区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY STEM CELLS Pub Date : 2023-12-14 DOI:10.1093/stmcls/sxad071
Jing Pu, Satoshi Kofuji, Yoshimi Okamoto-Uchida, Keiko Danzaki, Ruoxing Yu, Akira Suzuki, Satoshi Kitajima, Hiroshi Nishina
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引用次数: 0

摘要

在早期胚胎发生中,原始条纹(PrS)产生间胚层,对器官发生至关重要。然而,由于PrS是一种微小而短暂的组织,因此阐明其形成机制一直具有挑战性。基于PrS形成失败是致命的这一事实,我们对2个敲除小鼠数据库进行了全面筛选。我们鉴定了812个参与各种细胞功能和反应的基因,这些基因可能与PrS的形成有关,其中丰度最高的一类是“代谢”。在本研究中,我们重点研究了鞘脂代谢基因,并使用体外小鼠ES细胞分化系统研究了它们在PrS形成中的作用。我们在这里表明,升高的细胞内神经酰胺负调控PrS形成所必需的基因表达,反而诱导神经发生。此外,鞘氨醇-1-磷酸(一种神经酰胺衍生物)正向调节神经成熟。我们的结果表明神经酰胺调节PrS的形成和神经分化的诱导。
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Lethal Phenotype-Based Database Screening Identifies Ceramide as a Negative Regulator of Primitive Streak Formation.

In early embryogenesis, the primitive streak (PrS) generates the mesendoderm and is essential for organogenesis. However, because the PrS is a minute and transient tissue, elucidating the mechanism of its formation has been challenging. We performed comprehensive screening of 2 knockout mouse databases based on the fact that failure of PrS formation is lethal. We identified 812 genes involved in various cellular functions and responses that might be linked to PrS formation, with the category of greatest abundance being "Metabolism." In this study, we focused on genes of sphingolipid metabolism and investigated their roles in PrS formation using an in vitro mouse ES cell differentiation system. We show here that elevated intracellular ceramide negatively regulates gene expression essential for PrS formation and instead induces neurogenesis. In addition, sphingosine-1-phosphate (a ceramide derivative) positively regulates neural maturation. Our results indicate that ceramide regulates both PrS formation and the induction of neural differentiation.

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来源期刊
STEM CELLS
STEM CELLS 医学-生物工程与应用微生物
CiteScore
10.30
自引率
1.90%
发文量
104
审稿时长
3 months
期刊介绍: STEM CELLS, a peer reviewed journal published monthly, provides a forum for prompt publication of original investigative papers and concise reviews. STEM CELLS is read and written by clinical and basic scientists whose expertise encompasses the rapidly expanding fields of stem and progenitor cell biology. STEM CELLS covers: Cancer Stem Cells, Embryonic Stem Cells/Induced Pluripotent Stem (iPS) Cells, Regenerative Medicine, Stem Cell Technology: Epigenetics, Genomics, Proteomics, and Metabonomics, Tissue-Specific Stem Cells, Translational and Clinical Research.
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