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患有听力损失的MRL.MpJ-Fas(lpr)自身免疫小鼠的耳蜗DNA受体染色减少。

Decreased cochlear DNA receptor staining in MRL.MpJ-Fas(lpr) autoimmune mice with hearing loss.

作者信息

Kaylie D M, Hefeneider S H, Kempton J B, Siess D C, Vedder C T, Merkens L S, Trune D R

机构信息

Department of Otolaryngology-Head and Neck Surgery, Oregon Hearing Research Center, Oregon Health Sciences University, Portland, Oregon 97201-3998, USA.

出版信息

Laryngoscope. 2001 Jul;111(7):1275-80. doi: 10.1097/00005537-200107000-00025.

Abstract

OBJECTIVES

Previous studies of decreased cochlear DNA binding in autoimmune mice suggested that antibodies against a cochlear cell surface DNA receptor cause autoimmune hearing loss. However, the presence of a cochlear DNA receptor has not been determined. Therefore, immunohistochemistry with an anti-DNA receptor antibody was performed on MRL.MpJ-Fas(lpr) (MRL/lpr) autoimmune mice to determine 1) which inner ear structures contain DNA receptors and 2) whether the receptor staining pattern changes as autoimmune disease progresses and hearing thresholds increase.

STUDY DESIGN

A prospective study of the progression of hearing loss in autoimmune mice and correlated alterations in immunostaining for the inner ear DNA receptor.

METHODS

One group of MRL/lpr mice (n = 10) was allowed to develop autoimmune disease, and auditory brainstem response (ABR) audiometry was performed at 4, 6, and 9 months of age to measure the progression of hearing loss. A second group (n = 5) was tested for ABR thresholds at 2 months of age and immediately killed to assess receptor staining before the onset of autoimmune disease and hearing loss. The inner ears from all mice were immunohistochemically stained with an anti-DNA receptor antibody, and a qualitative analysis of the staining of cochlear structures was performed.

RESULTS

Auditory brainstem response audiometry revealed a significant 20- to 30-dB elevation of thresholds as systemic disease progressed. Anti-DNA receptor staining was heaviest in the spiral ligament and less intense in the spiral ganglion and cochlear nerve. Both groups showed a similar pattern of staining in these structures. The stria vascularis and hair cells also stained in both groups. However, the stria cells of normal-hearing mice showed diffuse intracellular immunoreactivity, whereas older mice displayed less staining that was confined to the cell membranes.

CONCLUSIONS

The inner ears of MRL/lpr mice contain DNA receptors. Autoimmune hearing loss was correlated with weaker overall intracellular staining in the stria vascularis and hair cells but increased staining of the cell membranes. This suggested DNA receptors have impaired endocytosis and more receptors remain on the cell membrane, possibly as a result of binding by circulating autoantibodies.

摘要

目的

先前针对自身免疫小鼠耳蜗DNA结合减少的研究表明,针对耳蜗细胞表面DNA受体的抗体可导致自身免疫性听力损失。然而,耳蜗DNA受体是否存在尚未确定。因此,使用抗DNA受体抗体对MRL.MpJ-Fas(lpr)(MRL/lpr)自身免疫小鼠进行免疫组织化学分析,以确定:1)哪些内耳结构含有DNA受体;2)随着自身免疫性疾病进展和听力阈值升高,受体染色模式是否会发生变化。

研究设计

一项关于自身免疫小鼠听力损失进展及内耳DNA受体免疫染色相关变化的前瞻性研究。

方法

一组MRL/lpr小鼠(n = 10)任其发展自身免疫性疾病,并在4、6和9月龄时进行听性脑干反应(ABR)听力测定,以测量听力损失的进展情况。第二组(n = 5)在2月龄时检测ABR阈值,并立即处死,以评估自身免疫性疾病和听力损失发作前的受体染色情况。所有小鼠的内耳均用抗DNA受体抗体进行免疫组织化学染色,并对耳蜗结构的染色进行定性分析。

结果

听性脑干反应听力测定显示,随着全身性疾病进展,阈值显著升高20至30分贝。抗DNA受体染色在螺旋韧带中最重,在螺旋神经节和耳蜗神经中较弱。两组在这些结构中的染色模式相似。两组的血管纹和毛细胞也有染色。然而,听力正常小鼠的血管纹细胞显示弥漫性细胞内免疫反应性,而老年小鼠的染色较少,局限于细胞膜。

结论

MRL/lpr小鼠的内耳含有DNA受体。自身免疫性听力损失与血管纹和毛细胞总体细胞内染色较弱但细胞膜染色增加有关。这表明DNA受体的内吞作用受损,更多受体保留在细胞膜上,可能是由于循环自身抗体的结合所致。

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