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临床孤立性视神经炎病例中诱导型一氧化氮合酶和硝基酪氨酸的免疫组织化学证据

Immunohistochemical evidence of inducible nitric oxide synthase and nitrotyrosine in a case of clinically isolated optic neuritis.

作者信息

Tsoi Veda L, Hill Kenneth E, Carlson Noel G, Warner Judith E A, Rose John W

机构信息

Neurovirology Research Laboratory, Veterans Affairs Salt Lake City Health Care System, Salt Lake City, Utah 84148, USA.

出版信息

J Neuroophthalmol. 2006 Jun;26(2):87-94. doi: 10.1097/01.wno.0000223266.48447.1b.

Abstract

BACKGROUND

Optic neuritis (ON) is a demyelinating inflammation of the optic nerve that may occur as an isolated disease or related to multiple sclerosis (MS). There is little evidence of whether the immunohistochemistry of ON resembles that of typical cerebral MS lesions.

METHODS

Pathologic optic nerves were obtained from a patient who died of causes unrelated to ON after clinical recovery from clinically isolated ON. Normal control optic nerves were obtained from an eye bank. Normal and pathologic tissues were probed with antibodies to pathologic proteins including myelin basic protein (MBP) fragment, the inducible form of nitric oxide synthase (iNOS), macrophage markers CD14 and CD64, nitrotyrosine, and cyclooxygenase (COX-2). We also examined MBP, the oligodendrocyte marker cyclic nucleotide phosphodiesterase (CNPase), and glial fibrillary acidic protein.

RESULTS

In the affected pathologic nerve, iNOS-positive macrophages/microglia, iNOS-positive astrocytes, COX-2, and nitrotyrosine were observed. iNOS and COX-2 were occasionally observed in the unaffected nerve. Decreased expression of MBP and CNPase was seen in the pathologic optic nerves, along with evidence of gliosis and ongoing myelin degradation indicated by the presence of MBP fragment.

CONCLUSIONS

The immunohistochemistry of clinically isolated optic neuritis, as judged by this single case, resembles that of cerebral lesions of MS in showing abnormally high levels of iNOS and nitrotyrosine as well as other mediators of immune damage.

摘要

背景

视神经炎(ON)是一种视神经的脱髓鞘性炎症,可作为一种孤立性疾病发生,或与多发性硬化症(MS)相关。关于视神经炎的免疫组化是否类似于典型脑多发性硬化症病变,几乎没有证据。

方法

从一名临床孤立性视神经炎临床恢复后因与视神经炎无关的原因死亡的患者获取病理视神经。正常对照视神经取自眼库。用针对病理蛋白的抗体检测正常和病理组织,这些病理蛋白包括髓鞘碱性蛋白(MBP)片段、诱导型一氧化氮合酶(iNOS)、巨噬细胞标志物CD14和CD64、硝基酪氨酸和环氧化酶(COX-2)。我们还检测了MBP、少突胶质细胞标志物环核苷酸磷酸二酯酶(CNPase)和胶质纤维酸性蛋白。

结果

在受影响的病理神经中,观察到iNOS阳性巨噬细胞/小胶质细胞、iNOS阳性星形胶质细胞、COX-2和硝基酪氨酸。在未受影响的神经中偶尔观察到iNOS和COX-2。在病理视神经中可见MBP和CNPase表达降低,同时存在MBP片段表明有胶质增生和正在进行的髓鞘降解。

结论

根据这一单个病例判断,临床孤立性视神经炎的免疫组化与多发性硬化症脑病变的免疫组化相似,表现为iNOS和硝基酪氨酸以及其他免疫损伤介质水平异常升高。

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