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大脑中的细胞融合:前进两步,后退一步。

Cell fusion in the brain: two cells forward, one cell back.

作者信息

Kemp Kevin, Wilkins Alastair, Scolding Neil

机构信息

Multiple Sclerosis and Stem Cell Group, School of Clinical Sciences, University of Bristol, Neuroscience Office, Learning and Research Building, Southmead Hospital, Bristol, BS10 5NB, UK,

出版信息

Acta Neuropathol. 2014 Nov;128(5):629-38. doi: 10.1007/s00401-014-1303-1. Epub 2014 Jun 5.

Abstract

Adult stem cell populations, notably those which reside in the bone marrow, have been shown to contribute to several neuronal cell types in the rodent and human brain. The observation that circulating bone marrow cells can migrate into the central nervous system and fuse with, in particular, cerebellar Purkinje cells has suggested, at least in part, a potential mechanism behind this process. Experimentally, the incidence of cell fusion in the brain is enhanced with age, radiation exposure, inflammation, chemotherapeutic drugs and even selective damage to the neurons themselves. The presence of cell fusion, shown by detection of increased bi-nucleated neurons, has also been described in a variety of human central nervous system diseases, including both multiple sclerosis and Alzheimer's disease. Accumulating evidence is therefore raising new questions into the biological significance of cell fusion, with the possibility that it represents an important means of cell-mediated neuroprotection or rescue of highly complex neurons that cannot be replaced in adult life. Here, we discuss the evidence behind this phenomenon in the rodent and human brain, with a focus on the subsequent research investigating the physiological mechanisms of cell fusion underlying this process. We also highlight how these studies offer new insights into endogenous neuronal repair, opening new exciting avenues for potential therapeutic interventions against neurodegeneration and brain injury.

摘要

成体干细胞群体,尤其是存在于骨髓中的那些干细胞,已被证明可分化为啮齿动物和人类大脑中的多种神经元细胞类型。循环骨髓细胞能够迁移至中枢神经系统并与小脑浦肯野细胞融合,这一现象至少部分地揭示了该过程背后的潜在机制。实验表明,随着年龄增长、辐射暴露、炎症、化疗药物作用甚至神经元自身的选择性损伤,大脑中细胞融合的发生率会增加。在包括多发性硬化症和阿尔茨海默病在内的多种人类中枢神经系统疾病中,也发现了通过检测双核神经元增多所显示的细胞融合现象。因此,越来越多的证据引发了关于细胞融合生物学意义的新问题,即细胞融合可能是细胞介导的神经保护或拯救成年后无法替代的高度复杂神经元的重要方式。在此,我们讨论啮齿动物和人类大脑中这一现象背后的证据,重点关注后续研究中对该过程潜在的细胞融合生理机制的探究。我们还强调了这些研究如何为内源性神经元修复提供新见解,为针对神经退行性变和脑损伤的潜在治疗干预开辟了令人兴奋的新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29f/4201757/0caa2f80b7f5/401_2014_1303_Fig1_HTML.jpg

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