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中枢神经系统神经胶质亚类对磁性粒子摄取的差异:对神经组织工程的影响。

Differences in magnetic particle uptake by CNS neuroglial subclasses: implications for neural tissue engineering.

机构信息

Cellular & Neural Engineering Group, Institute for Science & Technology in Medicine, Keele University, Staffordshire, ST5 5BG, UK.

出版信息

Nanomedicine (Lond). 2013 Jun;8(6):951-68. doi: 10.2217/nnm.12.145. Epub 2012 Nov 22.

Abstract

AIM

To analyze magnetic particle uptake and intracellular processing by the four main non-neuronal subclasses of the CNS: oligodendrocyte precursor cells; oligodendrocytes; astrocytes; and microglia.

MATERIALS & METHODS: Magnetic particle uptake and processing were studied in rat oligodendrocyte precursor cells and oligodendrocytes using fluorescence and transmission electron microscopy, and the results collated with previous data from rat microglia and astrocyte studies. All cells were derived from primary mixed glial cultures.

RESULTS

Significant intercellular differences were observed between glial subtypes: microglia demonstrate the most rapid/extensive particle uptake, followed by astrocytes, with oligodendrocyte precursor cells and oligodendrocytes showing significantly lower uptake. Ultrastructural analyses suggest that magnetic particles are extensively degraded in microglia, but relatively stable in other cells.

CONCLUSION

Intercellular differences in particle uptake and handling exist between the major neuroglial subtypes. This has important implications for the utility of the magnetic particle platform for neurobiological applications including genetic modification, transplant cell labeling and biomolecule delivery to mixed CNS cell populations.

摘要

目的

分析四种主要的中枢神经系统非神经元亚型(少突胶质前体细胞;少突胶质细胞;星形胶质细胞;和小胶质细胞)对磁颗粒的摄取和细胞内处理。

材料与方法

使用荧光和透射电子显微镜研究大鼠少突胶质前体细胞和少突胶质细胞中的磁颗粒摄取和处理,并将结果与之前大鼠小胶质细胞和星形胶质细胞研究的数据进行汇总。所有细胞均来自原代混合神经胶质培养物。

结果

观察到不同胶质细胞亚型之间存在显著的细胞间差异:小胶质细胞表现出最快/最广泛的颗粒摄取,其次是星形胶质细胞,少突胶质前体细胞和少突胶质细胞的摄取明显较低。超微结构分析表明,磁颗粒在小胶质细胞中被广泛降解,但在其他细胞中相对稳定。

结论

主要神经胶质亚型之间在颗粒摄取和处理方面存在细胞间差异。这对于磁性颗粒平台在神经生物学应用中的应用具有重要意义,包括基因修饰、移植细胞标记和生物分子递送至混合中枢神经系统细胞群体。

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