1 Columbia University College of Physicians and Surgeons, New York, New York, USA.
2 Columbia University Medical Center/New York Presbyterian, New York, New York, USA.
Otolaryngol Head Neck Surg. 2019 Jul;161(1):111-117. doi: 10.1177/0194599819831289. Epub 2019 Feb 19.
Recurrent laryngeal nerve (RLN) injury causes vocal fold paralysis from which functional recovery is typically absent due to nonselective reinnervation. This study investigates expression of axon guidance cues and their modulators relative to the chronology of reinnervation by examining the expression of glial-derived neurotrophic factor (GDNF), netrin 1, and laminin 111 (LAMA1) in nonpooled laryngeal muscles. This study is the first to describe the post-RLN injury expression pattern of LAMA1, a target of particular interest as it has been shown to switch netrin 1-mediated growth cone attraction to repulsion.
Animal experiment (rat model).
Basic science laboratory.
The right RLNs of 64 female Sprague-Dawley rats were transected, with sacrifice at 1, 3, 7, 21, 28, and 56 days postinjury (DPI). Single-animal messenger RNA was isolated from the ipsilateral posterior cricoarytenoid (PCA), lateral thyroarytenoid (LTA), and medial thyroarytenoid (MTA) for quantitative reverse transcription polymerase chain reaction (qRT-PCR) analysis. Immunostaining for LAMA1 expression was performed in the same muscles.
LAMA1 was elevated in the PCA at 3 to 56 DPI, LTA at 7 DPI, and MTA at 14 and 28 DPI. This correlates with the chronology of laryngeal reinnervation. Using a new protocol, single-animal muscle qRT-PCR possible and expression results for GDNF and netrin 1 were similar to previous pooled investigations.
Reliable qRT-PCR is possible with single rat laryngeal muscles. The expression of netrin 1 and LAMA1 is chronologically coordinated with muscle innervation in the LTA and MTA. This suggests that LAMA1 may influence netrin 1 to repel axons and delay LTA and MTA reinnervation.
喉返神经(RLN)损伤可导致声带麻痹,由于非选择性再支配,其功能通常无法恢复。本研究通过检查神经胶质细胞衍生神经营养因子(GDNF)、轴突导向因子 1(netrin 1)和层粘连蛋白 111(LAMA1)的表达,研究 RLN 损伤后再支配的时间顺序,探讨轴突导向因子及其调节剂的表达。本研究首次描述了 LAMA1 的损伤后表达模式,作为 netrin 1 介导的生长锥吸引向排斥转变的靶点,LAMA1 特别令人感兴趣。
动物实验(大鼠模型)。
基础科学实验室。
将 64 只雌性 Sprague-Dawley 大鼠右侧 RLN 切断,分别于损伤后 1、3、7、21、28 和 56 天(DPI)处死。对单侧后环杓肌(PCA)、外侧甲杓肌(LTA)和内侧甲杓肌(MTA)的单个动物信使 RNA 进行分离,用于定量逆转录聚合酶链反应(qRT-PCR)分析。在相同的肌肉中进行 LAMA1 表达的免疫染色。
LAMA1 在 PCA 中的表达在 3 至 56 DPI 期间升高,在 LTA 中的表达在 7 DPI 期间升高,在 MTA 中的表达在 14 和 28 DPI 期间升高。这与喉神经再支配的时间顺序相关。使用新方案,单个动物肌肉 qRT-PCR 是可行的,GDNF 和 netrin 1 的表达结果与之前的 pooled 研究相似。
使用单个大鼠喉肌进行可靠的 qRT-PCR 是可能的。netrin 1 和 LAMA1 的表达与 LTA 和 MTA 中的肌肉神经支配在时间上是协调一致的。这表明 LAMA1 可能影响 netrin 1 排斥轴突并延迟 LTA 和 MTA 的再支配。