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T 盒转录因子 21 表达于神经肌肉接头的终末 Schwann 细胞。

T-box transcription factor 21 is expressed in terminal Schwann cells at the neuromuscular junction.

机构信息

Division of Plastic Surgery, Department of Surgery, Washington University School of Medicine, Saint Louis, Missouri, USA.

出版信息

Muscle Nerve. 2021 Jul;64(1):109-115. doi: 10.1002/mus.27257. Epub 2021 May 12.

Abstract

INTRODUCTION/AIMS: Terminal Schwann cells (tSCs) are nonmyelinating Schwann cells present at the neuromuscular junction (NMJ) with multiple integral roles throughout their lifespan. There is no known gene differentiating tSCs from myelinating Schwann cells, making their isolation and investigation challenging. In this work we investigated genes expressed within tSCs.

METHODS

A novel dissection technique was utilized to isolate the tSC-containing NMJ band from the sternomastoid muscles of S100-GFP mice. RNA was isolated from samples containing: (a) NMJ bands (tSCs with nerve and muscle), (b) nerve, and (c) muscle, and microarray genetic expression analysis was conducted. Data were validated by quantitative real-time polymerase chain reaction (qRT-PCR) and immunofluorescent staining. To identify genes specific to tSCs compared with other NMJ components, analysis of variance and rank-order analysis were performed using the Partek Genomic Suite.

RESULTS

Microarray analysis of the tSC-enriched NMJ band revealed upregulation (by 4- to 12-fold) of several genes unique to the NMJ compared with muscle or nerve parts alone (P < .05). Among these genes, Tbx21 (or T-bet) was identified, which showed a 12-fold higher expression at the NMJ compared with sciatic nerve (P < .002). qRT-PCR analysis showed Tbx21 mRNA expression was over ninefold higher (P < .05) in the NMJ relative to muscle and nerve. Tbx21 protein colocalized with tSCs and was not noted in myelinating SCs from sciatic nerve.

DISCUSSION

We found TBX21 to be expressed in tSCs. Additional studies will be performed to determine the functional significance of TBX21 in tSCs. These studies may enhance the investigative tools available to modulate tSCs to improve motor recovery after nerve injury.

摘要

简介/目的:终末施万细胞(tSCs)是存在于神经肌肉接头(NMJ)的非髓鞘施万细胞,在其整个生命周期中具有多种重要作用。目前还没有已知的基因可以将 tSCs 与髓鞘施万细胞区分开来,这使得它们的分离和研究具有挑战性。在这项工作中,我们研究了在 tSCs 中表达的基因。

方法

利用一种新的解剖技术从 S100-GFP 小鼠的胸锁乳突肌中分离出包含 tSCs 的 NMJ 带。从包含以下样本的样品中提取 RNA:(a)NMJ 带(带有神经和肌肉的 tSCs)、(b)神经和(c)肌肉,并进行微阵列基因表达分析。通过定量实时聚合酶链反应(qRT-PCR)和免疫荧光染色验证数据。为了鉴定与其他 NMJ 成分相比特异性表达于 tSCs 的基因,使用 Partek Genomic Suite 进行方差分析和秩次分析。

结果

对富含 tSCs 的 NMJ 带的微阵列分析显示,与单独的肌肉或神经部分相比,几种仅在 NMJ 中上调(上调 4-12 倍)(P<.05)。在这些基因中,Tbx21(或 T-bet)被鉴定为与坐骨神经相比在 NMJ 中表达上调 12 倍(P<.002)。qRT-PCR 分析显示,NMJ 中 Tbx21 mRNA 的表达比肌肉和神经高 9 倍以上(P<.05)。Tbx21 蛋白与 tSCs 共定位,而在坐骨神经中的髓鞘施万细胞中未见表达。

讨论

我们发现 TBX21 在 tSCs 中表达。将进行进一步的研究以确定 TBX21 在 tSCs 中的功能意义。这些研究可能会增强可用于调节 tSCs 以改善神经损伤后运动功能恢复的研究工具。

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