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表达Iba1的骨髓源性细胞作为常驻组织巨噬细胞组成性地存在于小鼠耳蜗中。

Bone marrow-derived cells expressing Iba1 are constitutively present as resident tissue macrophages in the mouse cochlea.

作者信息

Okano Takayuki, Nakagawa Takayuki, Kita Tomoko, Kada Shinpei, Yoshimoto Momoko, Nakahata Tatsutoshi, Ito Juichi

机构信息

Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

J Neurosci Res. 2008 Jun;86(8):1758-67. doi: 10.1002/jnr.21625.

Abstract

Immune-mediated inner ear disorder has been well established as a clinical entity; however, the innate immune system of the inner ear is a poorly understood area of research with high clinical and immunological importance. Although the presence of resident tissue macrophages in the inner ear has been suggested, there has been some controversy. In this study, we analyzed the origin of cochlear resident macrophages and the contribution of hematopoietic bone marrow (BM) to the recruitment of macrophages in the cochlea. To visualize the localization of BM-derived cells, BM chimeric mice were made by transplantation of hematopoietic stem cells, which were genetically labeled with enhanced green fluorescent protein, into lethally irradiated C57BL/6 mice. The distribution and characteristics of BM-derived cells in the mouse cochlea were studied immunohistochemically. We successfully identified the constitutive presence of tissue resident macrophages in the spiral ligament and spiral ganglion that are derived from BM in larger numbers than previously reported. Moreover, cochlear resident macrophages gradually turn over for several months during steady-state replacement by BM-derived cells, and the number of cochlear macrophages immediately increased in response to local surgical stress. The present findings demonstrate the hematopoietic origin of cochlear resident and infiltrating macrophages. Our study provides a novel anatomical and immunological basis for the inner ear and indicates that the cochlear resident macrophages would be a therapeutic target in inner ear disorders.

摘要

免疫介导性内耳疾病已被确认为一种临床实体;然而,内耳的先天性免疫系统是一个研究较少但具有高度临床和免疫学重要性的领域。尽管有人提出内耳存在常驻组织巨噬细胞,但仍存在一些争议。在本研究中,我们分析了耳蜗常驻巨噬细胞的起源以及造血骨髓(BM)对耳蜗巨噬细胞募集的贡献。为了可视化BM来源细胞的定位,通过将用增强型绿色荧光蛋白进行基因标记的造血干细胞移植到经致死剂量照射的C57BL/6小鼠中,制备了BM嵌合小鼠。通过免疫组织化学研究了小鼠耳蜗中BM来源细胞的分布和特征。我们成功鉴定出螺旋韧带和螺旋神经节中存在大量源自BM的组织常驻巨噬细胞,其数量比先前报道的要多。此外,在稳态更替过程中,耳蜗常驻巨噬细胞会在数月内逐渐被BM来源的细胞替代,并且耳蜗巨噬细胞的数量会因局部手术应激而立即增加。目前的研究结果证明了耳蜗常驻和浸润巨噬细胞的造血起源。我们的研究为内耳提供了新的解剖学和免疫学基础,并表明耳蜗常驻巨噬细胞可能成为内耳疾病的治疗靶点。

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