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海七鳃鳗幼体脊髓再生过程中动态的小胶质细胞/巨噬细胞浸润

Dynamic microglia/macrophage infiltration during spinal cord regeneration in larval sea lamprey.

作者信息

Guadarrama Eduardo, Heisse Logan W, Morgan Jennifer R, Katz Hilary R

机构信息

The Eugene Bell Center for Regenerative Biology and Tissue Engineering, Marine Biological Laboratory, Woods Hole, Massachusetts, USA.

Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.

出版信息

Ann N Y Acad Sci. 2025 Jul;1549(1):250-259. doi: 10.1111/nyas.15396. Epub 2025 Jun 25.

Abstract

Both mammals and non-mammalian vertebrates display neuroimmune interactions after spinal cord injury (SCI). However, the impact of the immune response on neural regeneration remains unclear as it includes both proregenerative and inhibitory processes. To begin to understand how neuroimmune interactions influence central nervous system (CNS) regeneration, we examined the distribution of microglia/macrophages in relation to regenerating axons in larval sea lamprey (Petromyzon marinus), a non-mammalian vertebrate that exhibits robust axon and synapse regeneration after SCI. The relationship between microglia/macrophages and spinal axons was examined in cryosections of control and transected spinal cords using immunofluorescence. SCI significantly increased microglia/macrophage density within the spinal cord, as shown by isolectin B labeling. At 11 weeks post-injury (WPI), microglia/macrophages made physical contacts with regenerating axons, on average a three-fold increase compared to controls. These results are consistent with the conclusion that microglia/macrophage infiltration is associated with axon regeneration. Understanding the importance of these neuroimmune interactions could bring insight into cellular and molecular mechanisms that promote regeneration in the mammalian CNS.

摘要

哺乳动物和非哺乳动物脊椎动物在脊髓损伤(SCI)后均表现出神经免疫相互作用。然而,免疫反应对神经再生的影响仍不清楚,因为它既包括促进再生的过程,也包括抑制过程。为了开始理解神经免疫相互作用如何影响中枢神经系统(CNS)再生,我们研究了幼虫海七鳃鳗(Petromyzon marinus)中与再生轴突相关的小胶质细胞/巨噬细胞的分布,海七鳃鳗是一种非哺乳动物脊椎动物,在脊髓损伤后表现出强大的轴突和突触再生能力。使用免疫荧光法在对照和横断脊髓的冰冻切片中研究了小胶质细胞/巨噬细胞与脊髓轴突之间的关系。如异凝集素B标记所示,脊髓损伤显著增加了脊髓内小胶质细胞/巨噬细胞的密度。在损伤后11周(WPI),小胶质细胞/巨噬细胞与再生轴突发生物理接触,与对照组相比平均增加了三倍。这些结果与小胶质细胞/巨噬细胞浸润与轴突再生相关的结论一致。了解这些神经免疫相互作用的重要性可能有助于深入了解促进哺乳动物中枢神经系统再生的细胞和分子机制。

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