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JNJ-10397049对神经前体细胞增殖和分化影响的研究

A study on the effect of JNJ-10397049 on proliferation and differentiation of neural precursor cells.

作者信息

Karami Neda, Azari Hassan, Rahimi Moosa, Aligholi Hadi, Kalantari Tahereh

机构信息

Division of Medical Biotechnology, Department of Laboratory Sciences, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.

Diagnostic Laboratory Sciences and Technology Research Center, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Anat Cell Biol. 2022 Jun 30;55(2):179-189. doi: 10.5115/acb.21.202. Epub 2022 Apr 25.

Abstract

The orexin 2 receptor plays a central role in maintaining sleep and wakefulness. Recently, it has been shown that sleep and wakefulness orchestrate the proliferation and differentiation of oligodendrocytes. Here, we explored the role of a selective orexin 2 receptor antagonist (JNJ-10397049) in proliferation and differentiation of neural progenitor cells (NPCs). We evaluated the proliferation potential of NPCs after exposure to different concentrations of JNJ-10397049 by using 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide and neurosphere assays. Moreover, the expression of differentiation markers was assessed by immunocytochemistry and real-time polymerase chain reaction. JNJ-10397049 significantly increased the proliferation of NPCs at lower concentrations. In addition, orexin 2 receptor antagonist facilitated progression of differentiation of NPCs towards oligodendroglial lineage by considerable expression of Olig2 and 2',3'-cyclic-nucleotide 3'-phosphodiesterase as well as decreased expression of nestin marker. The results open a new avenue for future investigations in which the production of more oligodendrocytes from NPCs is needed.

摘要

食欲素2受体在维持睡眠和觉醒中起核心作用。最近,研究表明睡眠和觉醒调控少突胶质细胞的增殖和分化。在此,我们探究了选择性食欲素2受体拮抗剂(JNJ - 10397049)在神经祖细胞(NPCs)增殖和分化中的作用。我们通过使用3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐和神经球试验,评估了暴露于不同浓度JNJ - 10397049后NPCs的增殖潜力。此外,通过免疫细胞化学和实时聚合酶链反应评估分化标志物的表达。较低浓度的JNJ - 10397049显著增加了NPCs的增殖。此外,食欲素2受体拮抗剂通过显著表达少突胶质细胞转录因子2(Olig2)和2',3'-环核苷酸3'-磷酸二酯酶以及降低巢蛋白标志物的表达,促进NPCs向少突胶质细胞谱系的分化进程。这些结果为未来需要从NPCs产生更多少突胶质细胞的研究开辟了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/685b/9256489/db8b5765bb94/acb-55-2-179-f1.jpg

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