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一种从成年小鼠大脑中分离小胶质细胞的简单方法。

A simple protocol for isolating microglia from adult mouse brain.

作者信息

Chakrabarti Sudipta, Gorai Sukhamoy, Pahan Kalipada

机构信息

Department of Neurological Sciences, Rush University Medical Center, Chicago, USA.

Division of Research and Development, Jesse Brown Veterans Affairs Medical Center, Chicago, USA.

出版信息

NeuroImmune Pharm Ther. 2023 Aug 2;2(3):293-300. doi: 10.1515/nipt-2023-0014. eCollection 2023 Sep.

Abstract

OBJECTIVES

Although microglia are activated in adult and aged brains resulting in neurodegenerative and neuroinflammatory disorders, most of the cell culture studies on microglia deal with neonatal microglia because of ease of isolation. Microglia could be isolated from adult brains, but it requires separation by density gradient centrifugation, magnetic beads, etc. Here, we describe a simple protocol of isolating highly purified microglia from adult mouse brains.

METHODS

Our protocol involves dilution with sterile PBS or media, regular centrifugation, and plating on poly-D-lysine-coated flasks.

RESULTS

These adult microglia expressed the inducible nitric oxide synthase in response to preformed α-syn fibril, an etiological reagent of Parkinson's disease, and bacterial lipopolysaccharides, one of the prototype proinflammatory stimuli. Moreover, these adult microglia exhibited phagocytosis, which was stimulated by LPS treatment.

CONCLUSIONS

These results suggest that adult microglia isolated by our procedure are functional and that these adult microglia could be used for studies related to neurodegenerative disorders.

摘要

目的

尽管小胶质细胞在成年和老年大脑中被激活会导致神经退行性和神经炎症性疾病,但由于易于分离,大多数关于小胶质细胞的细胞培养研究都涉及新生小胶质细胞。小胶质细胞可以从成年大脑中分离出来,但需要通过密度梯度离心、磁珠等方法进行分离。在此,我们描述了一种从成年小鼠大脑中分离高度纯化小胶质细胞的简单方案。

方法

我们的方案包括用无菌PBS或培养基稀释、常规离心以及接种到聚-D-赖氨酸包被的培养瓶上。

结果

这些成年小胶质细胞在帕金森病的病因试剂——预先形成的α-突触核蛋白纤维和原型促炎刺激物之一的细菌脂多糖的刺激下,表达诱导型一氧化氮合酶。此外,这些成年小胶质细胞表现出吞噬作用,脂多糖处理可刺激这种作用。

结论

这些结果表明,通过我们的方法分离的成年小胶质细胞具有功能,并且这些成年小胶质细胞可用于与神经退行性疾病相关的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb2/10474378/c458fc860ff0/j_nipt-2023-0014_fig_001.jpg

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