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新生鼠脑缺氧缺血模型中精氨酸酶同工酶的变化。

Changes in arginase isoforms in a murine model of neonatal brain hypoxia-ischemia.

机构信息

Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.

Department of Neurology, University of California San Francisco, San Francisco, CA, USA.

出版信息

Pediatr Res. 2021 Mar;89(4):830-837. doi: 10.1038/s41390-020-0978-3. Epub 2020 May 28.

Abstract

BACKGROUND

Arginases (ARG isoforms, ARG-1/ARG-2) are key regulatory enzymes of inflammation and tissue repair; however, their role after neonatal brain hypoxia (H) and hypoxia-ischemia (HI) remains unknown.

METHODS

C57BL/6 mice subjected to the Vannucci procedure on postnatal day (P9) were sacrificed at different timepoints. The degree of brain damage was assessed histologically. ARG spatiotemporal localization was determined via immunohistochemistry. ARG expression was measured by Western blot and activity spectrophotometrically.

RESULTS

ARG isoform expression increased during neurodevelopment (P9-P17) in the cortex and hippocampus. This was suppressed with H and HI only in the hippocampus. In the cortex, both isoforms increased with H alone and only ARG-2 increased with HI at 3 days. ARG activity during neurodevelopment remained unchanged, but increased at 1 day with H and not HI. ARG-1 localized with microglia at the injury site as early as 4 h after injury, while ARG-2 localized with neurons.

CONCLUSIONS

ARG isoform expression increases with age from P9 to P17, but is suppressed by injury specifically in the hippocampus and not in the cortex. Both levels and activity of ARG isoforms increase with H, while ARG-1 immunolabelling is upregulated in the HI cortex. Evidently, ARG isoforms in the brain differ in spatiotemporal localization, expression, and activity during neurodevelopment and after injury.

IMPACT

Arginase isoforms change during neurodevelopment and after neonatal brain HI. This is the first study investigating the key enzymes of inflammation and tissue repair called arginases following murine neonatal brain HI. The highly region- and cell-specific expression suggests the possibility of specific functions of arginases. ARG-1 in microglia at the injury site may regulate neuroinflammation, while ARG-2 in neurons of developmental structures may impact neurodevelopment. While further studies are needed to describe the exact role of ARGs after neonatal brain HI, our study adds valuable data on anatomical localization and expression of ARGs in brain during development and after stroke.

摘要

背景

精氨酸酶(ARG 同工型,ARG-1/ARG-2)是炎症和组织修复的关键调节酶;然而,它们在新生儿脑缺氧(H)和缺氧缺血(HI)后的作用仍不清楚。

方法

对生后第 9 天(P9)的 C57BL/6 小鼠进行 Vannucci 手术,在不同时间点处死。通过组织学评估脑损伤程度。通过免疫组织化学确定 ARG 的时空定位。通过 Western blot 和活性分光光度法测量 ARG 的表达。

结果

ARG 同工型的表达在皮质和海马体的神经发育过程中(P9-P17)增加。这种表达在海马体中仅在 H 和 HI 后受到抑制。在皮质中,两种同工型仅在 H 单独存在时增加,而仅在 HI 后 3 天 ARG-2 增加。神经发育过程中的 ARG 活性保持不变,但在 H 后 1 天增加,而 HI 则没有。ARG-1 在损伤后 4 小时即可与损伤部位的小胶质细胞定位,而 ARG-2 则与神经元定位。

结论

ARG 同工型的表达从 P9 到 P17 随年龄增长而增加,但仅在海马体而非皮质中受到损伤的抑制。两种 ARG 同工型的水平和活性均随 H 增加,而 HI 皮质中的 ARG-1 免疫标记物上调。显然,ARG 同工型在脑内的时空定位、表达和活性在神经发育和损伤后存在差异。

影响

精氨酸酶同工型在神经发育过程中和新生儿脑 HI 后发生变化。这是首次研究称为精氨酸酶的炎症和组织修复的关键酶在新生鼠脑 HI 后的情况。高度区域和细胞特异性表达表明精氨酸酶可能具有特定的功能。损伤部位小胶质细胞中的 ARG-1 可能调节神经炎症,而发育结构中神经元中的 ARG-2 可能影响神经发育。虽然还需要进一步的研究来描述新生儿脑 HI 后 ARG 的确切作用,但我们的研究为大脑在发育过程中和中风后 ARG 的解剖定位和表达提供了有价值的数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/7704631/389f0b263136/nihms-1596129-f0001.jpg

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