首页> 外文期刊>Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology >Increased gene expression of growth associated protein-43 in skin of patients with early-stage peripheral neuropathies
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Increased gene expression of growth associated protein-43 in skin of patients with early-stage peripheral neuropathies

机译:早期周围神经病患者皮肤中生长相关蛋白43的基因表达增加

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摘要

Growth associated protein-43 (GAP-43) is one of the neural proteins associated with nerve injury that is upregulated after nerve injury. To investigate whether GAP-43 quantification in skin biopsies would differentiate subtypes of peripheral neuropathies, we analyzed GAP-43 expression in skin from the lateral thigh and the distal leg. We prospectively enrolled 130 patients with peripheral neuropathies and compared data with healthy controls. Intraepidermal nerve fiber density (IENFD) was determined using antibodies against protein gene product 9.5 (PGP 9.5); anti-GAP-43 antibodies were applied to visualize regenerating nerve fibers. PGP 9.5 and GAP-43 gene expression was analyzed using qRT-PCR. Patients with neuropathies had a generalized reduction of IENFD and GAP-43 immunoreactive fibers compared to controls (p < 0.01). In contrast, cutaneous GAP-43 gene expression was increased in proximal skin in patients (p < 0.05), particularly when disease duration was short (<3 years; p < 0.01). While fiber density for both markers decreased with age in healthy skin (p < 0.01), age-dependent reduction of skin innervation was absent in neuropathies. Diagnostic subgroups and neuropathic pain had no influence on skin innervation. We conclude that peripheral neuropathies lead to an initial increase in GAP-43 gene expression as a potential mechanism of regeneration, which is not sustained in neuropathies of long duration. (C) 2015 Elsevier B.V. All rights reserved.
机译:生长相关蛋白43(GAP-43)是与神经损伤相关的神经蛋白之一,在神经损伤后被上调。为了研究皮肤活检中的GAP-43定量是否会区分周围神经病变的亚型,我们分析了大腿外侧和远端腿部皮肤中GAP-43的表达。我们前瞻性地招募了130名周围神经病患者,并将数据与健康对照进行了比较。使用针对蛋白质基因产物9.5(PGP 9.5)的抗体测定表皮神经纤维密度(IENFD);抗GAP-43抗体被用于可视化再生神经纤维。使用qRT-PCR分析PGP 9.5和GAP-43基因表达。与对照组相比,神经病患者的IENFD和GAP-43免疫反应性纤维普遍减少(p <0.01)。相反,患者近端皮肤的皮肤GAP-43基因表达增加(p <0.05),特别是当疾病持续时间短(<3年; p <0.01)时。尽管健康皮肤中两种标记物的纤维密度均随着年龄的增长而降低(p <0.01),但神经病变中没有年龄依赖性的皮肤神经支配减少。诊断亚组和神经性疼痛对皮肤神经没有影响。我们得出的结论是,周围神经病会导致GAP-43基因表达的最初增加,这是潜在的再生机制,在长期持续的神经病中并未持续存在。 (C)2015 Elsevier B.V.保留所有权利。

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