Columbia University Irving Medical Center/New York Presbyterian, Department of Otolaryngology Head & Neck Surgery, New York, NY, USA.
Columbia University Irving Medical Center/New York Presbyterian, Department of Otolaryngology Head & Neck Surgery, New York, NY, USA; Columbia University Irving Medical Center/New York Presbyterian, The Center for Voice and Swallowing, Department of Otolaryngology Head & Neck Surgery, New York, NY, USA.
Neurosci Lett. 2022 Jun 11;781:136658. doi: 10.1016/j.neulet.2022.136658. Epub 2022 Apr 25.
Laminin-111 is a basement membrane protein that participates in motor innervation and reinnervation. During axonal pathfinding, laminin-111 interacts with netrin-1 (NTN1) and changes its attractant growth cone properties into repulsion. While previous models of recurrent laryngeal nerve (RLN) transection show increased Laminin-111 and NTN1 production after injury, developmental expression in the larynx has not been defined. This study investigates the expression of laminin-111 in laryngeal muscles during primary laryngeal innervation of Sprague Dawley rats. Adult larynges and embryos were sectioned for immunohistochemistry with βIII-Tubulin, laminin subunit α-1 (LAMA1), NTN1, and α-bungarotoxin. Sections were processed for single-molecule inexpensive RNA fluorescence in situ hybridization analysis of LAMA1 mRNA. LAMA1 expression increased in all intrinsic laryngeal muscles, except the medial thyroarytenoid (MTA), at E20.5. At E20.5 there was increased expression in the lateral thyroarytenoid (LTA) and posterior cricoarytenoid (PCA) compared to the MTA. NTN1 upregulation was limited to the LTA and lateral cricoarytenoid (LCA) at E16.5 without any increase in the MTA or PCA. LAMA1 and NTN1 expression did not strictly follow expected patterns relative to the known timing of innervation and does not appear to be acting similarly to its role following RLN injury. These differences between developmental and post-injury innervation provide targets for investigations of therapeutics after nerve injury.
层粘连蛋白-111 是一种基底膜蛋白,参与运动神经支配和再支配。在轴突寻路过程中,层粘连蛋白-111 与轴突导向因子 1(NTN1)相互作用,将吸引性生长锥的特性改变为排斥性。虽然先前的喉返神经(RLN)横断模型显示损伤后层粘连蛋白-111 和 NTN1 的产生增加,但喉内的发育表达尚未确定。本研究探讨了 Sprague Dawley 大鼠喉初级神经支配过程中喉肌中层粘连蛋白-111 的表达。对成年和胚胎喉进行βIII-微管蛋白、层粘连蛋白亚基α-1(LAMA1)、NTN1 和α-银环蛇毒素免疫组织化学染色。对切片进行 LAMA1 mRNA 单分子廉价 RNA 荧光原位杂交分析。E20.5 时,除内侧杓状肌(MTA)外,所有固有喉肌中的 LAMA1 表达均增加。与 MTA 相比,E20.5 时外侧杓状肌(LTA)和后环杓肌(PCA)的表达增加。E16.5 时,NTN1 的上调仅限于 LTA 和外侧环杓肌(LCA),而 MTA 或 PCA 没有增加。LAMA1 和 NTN1 的表达与已知的神经支配时间并不完全一致,也似乎与其在 RLN 损伤后的作用不同。发育和损伤后神经支配之间的这些差异为神经损伤后治疗的研究提供了靶点。