Ebenezer Gigi J, Laast Victoria A, Dearman Brandon, Hauer Peter, Tarwater Patrick M, Adams Robert J, Zink M Christine, McArthur Justin C, Mankowski Joseph L
Department of Neurology, Johns Hopkins University, Baltimore, MD 21287-7609, USA.
J Comp Neurol. 2009 May 20;514(3):272-83. doi: 10.1002/cne.22019.
To characterize the regenerative pattern of cutaneous nerves in simian immunodeficiency virus (SIV)-infected and uninfected macaques, excisional axotomies were performed in nonglabrous skin at 14-day intervals. Samples were examined after immunostaining for the pan-axonal marker PGP 9.5 and the Schwann cell marker p75 nerve growth factor receptor. Collateral sprouting of axons from adjacent uninjured superficial dermal nerve bundles was the initial response to axotomy. Both horizontal collateral sprouts and dense vertical regeneration of axons from the deeper dermis led to complete, rapid reinnervation of the epidermis at the axotomy site. In contrast to the slower, incomplete reinnervation previously noted in humans after this technique, in both SIV-infected and uninfected macaques epidermal reinnervation was rapid and completed by 56 days postaxotomy. p75 was densely expressed on the Schwann cells of uninjured nerve bundles along the excision line and on epidermal Schwann cell processes. In both SIV-infected and uninfected macaques, Schwann cell process density was highest at the earliest timepoints postaxotomy and then declined at a similar rate. However, SIV-infection delayed epidermal nerve fiber regeneration and remodeling of new sprouts at every timepoint postaxotomy, and SIV-infected animals consistently had lower mean epidermal Schwann cell densities, suggesting that Schwann cell guidance and support of epidermal nerve fiber regeneration may account for altered nerve regeneration. The relatively rapid regeneration time and the completeness of epidermal reinnervation in this macaque model provides a useful platform for assessing the efficacy of neurotrophic or regenerative drugs for sensory neuropathies including those caused by HIV, diabetes mellitus, medications, and toxins.
为了描述感染和未感染猿猴免疫缺陷病毒(SIV)的猕猴皮肤神经的再生模式,在非无毛皮肤处每隔14天进行一次切除性轴突切断术。对样本进行免疫染色,检测泛轴突标记物PGP 9.5和施万细胞标记物p75神经生长因子受体,之后进行检查。来自相邻未受损浅表真皮神经束的轴突侧支发芽是对轴突切断术的初始反应。水平侧支芽和来自更深层真皮的轴突密集垂直再生导致轴突切断部位的表皮迅速完全重新神经支配。与此前该技术在人类中观察到的较慢、不完全的重新神经支配不同,在感染SIV和未感染SIV的猕猴中,表皮重新神经支配都很快,在轴突切断术后56天完成。p75在切除线沿线未受损神经束的施万细胞以及表皮施万细胞突起上密集表达。在感染SIV和未感染SIV的猕猴中,施万细胞突起密度在轴突切断术后最早的时间点最高,然后以相似的速率下降。然而,SIV感染在轴突切断术后的每个时间点都延迟了表皮神经纤维再生和新芽重塑,并且感染SIV的动物平均表皮施万细胞密度始终较低,这表明施万细胞对表皮神经纤维再生的引导和支持可能是神经再生改变的原因。该猕猴模型中相对较快的再生时间和表皮重新神经支配的完整性为评估神经营养或再生药物对包括由HIV、糖尿病、药物和毒素引起的感觉神经病变的疗效提供了一个有用的平台。