Jiang Yifeng, Du Zhen, Chen Long
Department of Stomatology, Shandong Medical College, Linyi, Shangdong 276002, P.R. China.
Department of Stomatology, Linyi People's Hospital, Linyi, Shandong 276000, P.R. China.
Exp Ther Med. 2018 Jan;15(1):383-386. doi: 10.3892/etm.2017.5350. Epub 2017 Oct 23.
Numerous factors, including trauma, tumors and myophagism, may lead to tongue defects, which are mostly repaired via muscular flaps. However, these methods cannot restore the muscular function and gustation function of the tongue. Intensive research on tongue development may offer useful clues for tongue regeneration based on tissue engineering or stem cell therapy. In the present study, staining results revealed that tongue muscle fibers became larger, mature and stronger, and the foliate and fungiform papillae also became mature from newborn to adult C57BL/6J genetic background mice. Immunofluorescence staining and polymerase chain reaction results revealed that C-kit was dynamically expressed in muscle cells, as well as in foliate and fungiform papilla cells from newborn to adult stages. The expression level decreased from P1 to P15 and increased at P90. The immunofluorescence staining results revealed that Ki-67 was expressed in muscle cells and papilla cells from newborn to adult stages, and high expression was observed at P6 and P15. In addition, the immunofluorescence staining results also demonstrated that msh homeobox 2 (Msx2) was dynamically expressed in postnatal tongue muscle cells; however, almost no expression was detected in papilla cells. There was relative high expression level of Msx2 at P1 and P6 stages, but this gradually decreased from P15, and it was expressed primarily in the muscle cells located in the marginal zone of the tongue at P90. These findings suggest that the amount of c-kit-expressing precursor cells in tongue muscle and papilla cells increases to promote tongue development at the early postnatal stage and to maintain homeostasis and functional adaptation of the tongue in the adult stage. Furthermore, Msx2 may serve an important role in postnatal tongue muscle development. The present study also suggests that C-kit and Msx2 may be used as cell markers for postnatal tongue regeneration and self-repair, and may provide an approach for developing treatment methods for tongue diseases with a postnatal onset.
包括创伤、肿瘤和食肌症在内的众多因素可能导致舌缺损,舌缺损大多通过肌瓣修复。然而,这些方法无法恢复舌的肌肉功能和味觉功能。对舌发育的深入研究可能为基于组织工程或干细胞疗法的舌再生提供有用线索。在本研究中,染色结果显示,从新生到成年的C57BL/6J基因背景小鼠,舌肌纤维变得更大、更成熟且更强壮,叶状乳头和菌状乳头也逐渐成熟。免疫荧光染色和聚合酶链反应结果显示,C-kit在从新生到成年阶段的肌肉细胞以及叶状和菌状乳头细胞中动态表达。其表达水平从出生后第1天(P1)到第15天下降,并在第90天增加。免疫荧光染色结果显示,Ki-67在从新生到成年阶段的肌肉细胞和乳头细胞中表达,在P6和P15时观察到高表达。此外,免疫荧光染色结果还表明,肌肉特异性同源盒2(Msx2)在出生后的舌肌细胞中动态表达;然而,在乳头细胞中几乎未检测到表达。Msx2在P1和P6阶段有相对较高的表达水平,但从P15开始逐渐下降,在P90时主要在位于舌边缘区域的肌肉细胞中表达。这些发现表明,舌肌和乳头细胞中表达C-kit的前体细胞数量增加,以促进出生后早期的舌发育,并在成年期维持舌的内环境稳定和功能适应。此外,Msx2可能在出生后的舌肌发育中起重要作用。本研究还表明,C-kit和Msx2可作为出生后舌再生和自我修复的细胞标志物,并可能为开发出生后发病的舌疾病治疗方法提供途径。