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损伤雌性大鼠脊髓中的浸润白细胞、活化小胶质细胞和星形胶质细胞引起铜蓝蛋白表达增加。

Increased ceruloplasmin expression caused by infiltrated leukocytes, activated microglia, and astrocytes in injured female rat spinal cords.

机构信息

Clinical Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu, People's Republic of China.

Anhui Key Laboratory of Tissue Transplantation, First Affiliated Hospital of Bengbu Medical College, Bengbu, People's Republic of China.

出版信息

J Neurosci Res. 2018 Jul;96(7):1265-1276. doi: 10.1002/jnr.24221. Epub 2018 Jan 29.

Abstract

Ceruloplasmin (Cp), an enzyme containing six copper atoms, has important roles in iron homeostasis and antioxidant defense. After spinal cord injury (SCI), the cellular components in the local microenvironment are very complex and include functional changes of resident cells and the infiltration of leukocytes. It has been confirmed that Cp is elevated primarily in astrocytes and to a lesser extent in macrophages following SCI in mice. However, its expression in other cell types is still not very clear. In this manuscript, we provide a sensible extension of these findings by examining this system within a female Sprague-Dawley rat model and expanding the scope of inquiry to include additional cell types. Quantitative reverse transcription polymerase chain reaction and Western blot analysis revealed that the Cp mRNA and protein in SCI tissue homogenates were quite consistent with prior publications. However, we observed that Cp was expressed not only in GFAP astrocytes (consistent with prior reports) but also in CD11b microglia, CNPase oligodendrocytes, NeuN neurons, CD45 leukocytes, and CD68 activated microglia/macrophages. Quantitative analysis proved that infiltrated leukocytes, activated microglia/macrophages, and astrocytes should be the major sources of increased Cp.

摘要

铜蓝蛋白(Cp)是一种含有 6 个铜原子的酶,在铁稳态和抗氧化防御中具有重要作用。脊髓损伤(SCI)后,局部微环境中的细胞成分非常复杂,包括固有细胞的功能变化和白细胞的浸润。已经证实,Cp 在 SCI 后主要在星形胶质细胞中升高,在小胶质细胞中升高程度较小。然而,其在其他细胞类型中的表达仍不是很清楚。在本手稿中,我们通过在雌性 Sprague-Dawley 大鼠模型中检查该系统,并将研究范围扩展到包括其他细胞类型,对这些发现进行了合理的扩展。定量逆转录聚合酶链反应和 Western blot 分析显示,SCI 组织匀浆中的 Cp mRNA 和蛋白与先前的出版物非常一致。然而,我们观察到 Cp 不仅在 GFAP 星形胶质细胞中表达(与先前的报道一致),而且在 CD11b 小胶质细胞、CNPase 少突胶质细胞、NeuN 神经元、CD45 白细胞和 CD68 活化的小胶质细胞/巨噬细胞中表达。定量分析证明,浸润的白细胞、活化的小胶质细胞/巨噬细胞和星形胶质细胞应该是 Cp 增加的主要来源。

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