Suppr超能文献

特定磷脂调节有丝分裂后细胞获得神经元和神经胶质细胞身份。

Specific Phospholipids Regulate the Acquisition of Neuronal and Astroglial Identities in Post-Mitotic Cells.

机构信息

Instituto de Biología Molecular y Celular de Rosario (IBR, CONICET) Ocampo y Esmeralda, Predio CONICET and Departamento de Ciencias Biológicas, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, 2000, Rosario, Argentina.

Brain Institute, Federal University of Rio Grande do Norte, Av. Nascimento de Castro 2155, 59056-450, Natal, Brazil.

出版信息

Sci Rep. 2018 Jan 11;8(1):460. doi: 10.1038/s41598-017-18700-4.

Abstract

Hitherto, the known mechanisms underpinning cell-fate specification act on neural progenitors, affecting their commitment to generate neuron or glial cells. Here, we show that particular phospholipids supplemented in the culture media modify the commitment of post-mitotic neural cells in vitro. Phosphatidylcholine (PtdCho)-enriched media enhances neuronal differentiation at the expense of astroglial and unspecified cells. Conversely, phosphatidylethanolamine (PtdEtn) enhances astroglial differentiation and accelerates astrocyte maturation. The ability of phospholipids to modify the fate of post-mitotic cells depends on its presence during a narrow time-window during cell differentiation and it is mediated by the selective activation of particular signaling pathways. While PtdCho-mediated effect on neuronal differentiation depends on cAMP-dependent kinase (PKA)/calcium responsive element binding protein (CREB), PtdEtn stimulates astrogliogenesis through the activation of the MEK/ERK signaling pathway. Collectively, our results provide an additional degree of plasticity in neural cell specification and further support the notion that cell differentiation is a reversible phenomenon. They also contribute to our understanding of neuronal and glial lineage specification in the central nervous system, opening up new avenues to retrieve neurogenic capacity in the brain.

摘要

迄今为止,已知的细胞命运决定机制作用于神经祖细胞,影响其生成神经元或神经胶质细胞的能力。在这里,我们发现培养介质中添加特定的磷脂可以改变体外有丝分裂后神经细胞的命运。富含卵磷脂(PtdCho)的培养基促进神经元分化,而牺牲星形胶质细胞和未分化细胞。相反,磷脂酰乙醇胺(PtdEtn)促进星形胶质细胞分化并加速其成熟。磷脂改变有丝分裂后细胞命运的能力取决于其在细胞分化的狭窄时间窗口内的存在,并且通过对特定信号通路的选择性激活来介导。虽然 PtdCho 对神经元分化的影响取决于 cAMP 依赖性激酶(PKA)/钙反应元件结合蛋白(CREB),但 PtdEtn 通过激活 MEK/ERK 信号通路刺激神经胶质发生。总之,我们的研究结果为神经细胞的特化提供了额外的可塑性,并进一步支持了细胞分化是一种可逆现象的观点。它们还有助于我们理解中枢神经系统中的神经元和神经胶质谱系特化,为在大脑中恢复神经发生能力开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5877/5765016/5a0e0f2dc725/41598_2017_18700_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验