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成肌细胞移植成功用于大鼠舌重建。

Successful myoblast transplantation in rat tongue reconstruction.

作者信息

Luxameechanporn Thongchai, Hadlock Tessa, Shyu Jeffrey, Cowan Douglas, Faquin William, Varvares Mark

机构信息

Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, USA.

出版信息

Head Neck. 2006 Jun;28(6):517-24. doi: 10.1002/hed.20325.

Abstract

BACKGROUND

Controversy exists regarding the success of myoblast transplantation. The purpose of this study was to determine the survival of transplanted myoblasts in a rat tongue reconstruction model by using fluorescently labeled myoblasts and surgical stains to mark the location of the pocket into which transplanted cells were delivered. We evaluated tongue histology after myoblast transplantation under the hypothesis that myoblast transplantation will promote muscle regeneration and result in minimal scar tissue formation.

METHODS

Sterile solutions of 1:10 India ink, 1% methylene blue, and 1% crystal violet were applied to the inner lining of a left-sided mucosa-sparing hemiglossectomy pocket. After air-drying, the hemiglossectomy defect was filled with collagen gel and closed. The tongues were evaluated histologically at 6 weeks. Next, myoblasts were cultured and labeled with three commercially available fluorescent dyes, 5-chloromethyl-fluorescein diacetate (CMFDA), chloromethylbenzamido (CM-DiI), and fluorescently labeled microspheres (FLMs), to determine which would optimally label myoblasts in a tongue reconstruction model. Next, Lewis rats underwent left hemiglossectomy, and the created pockets were coated with 1:10 India ink. Control animals received collagen gel alone, whereas experimental animals received labeled myoblast/collagen constructs into the tongue defect. Tongues were harvested at intervals to determine the presence of labeled fluorescent cells, the relative numbers of viable myoblasts, and the degree of scarring.

RESULTS

India ink coating of the hemiglossectomy pocket caused minimal inflammation and lasted longer than the other tested dyes. CMFDA and FLMs both successfully label myoblasts for transplantation. In vivo, donor cells were observed in all specimens at week 0 with increasing numbers of cells and muscle formation, determined by desmin immunofluorescence, after 6 weeks. There was less scar tissue contracture in the experimental group and a significant increase in the amount of desmin-stained muscle in the surgical defect.

CONCLUSIONS

India ink is an appropriate vehicle for intra-operative marking of a hemiglossectomy cavity. The introduction of myoblast/collagen constructs into the rat hemiglossectomy defect increases the amount of regenerated muscle, results in less scar contracture, and may increase meaningful tongue function.

摘要

背景

关于成肌细胞移植的成功率存在争议。本研究的目的是通过使用荧光标记的成肌细胞和手术染色剂来标记移植细胞所植入的腔隙位置,从而确定在大鼠舌重建模型中移植成肌细胞的存活情况。我们在成肌细胞移植后评估舌组织学情况,基于的假设是成肌细胞移植将促进肌肉再生并使瘢痕组织形成最小化。

方法

将1:10的印度墨水、1%的亚甲蓝和1%的结晶紫无菌溶液涂抹于左侧保留黏膜的半舌切除腔隙的内衬。风干后,用胶原凝胶填充半舌切除缺损并封闭。在6周时对舌进行组织学评估。接下来,培养成肌细胞并用三种市售荧光染料5-氯甲基荧光素二乙酸酯(CMFDA)、氯甲基苯甲酰胺(CM-DiI)和荧光标记微球(FLMs)进行标记,以确定哪种染料能在舌重建模型中最佳地标记成肌细胞。接下来,对Lewis大鼠进行左侧半舌切除术,并用1:10的印度墨水涂抹所形成的腔隙。对照动物仅接受胶原凝胶,而实验动物在舌缺损处接受标记的成肌细胞/胶原构建体。定期采集舌组织以确定标记荧光细胞的存在、存活成肌细胞的相对数量以及瘢痕形成程度。

结果

半舌切除腔隙的印度墨水涂层引起的炎症最小,且比其他测试染料持续时间更长。CMFDA和FLMs都成功地标记了用于移植的成肌细胞。在体内,在第0周时所有标本中均观察到供体细胞,6周后通过结蛋白免疫荧光确定细胞数量增加且有肌肉形成。实验组的瘢痕组织挛缩较少,手术缺损处结蛋白染色的肌肉量显著增加。

结论

印度墨水是半舌切除腔隙术中标记的合适载体。将成肌细胞/胶原构建体引入大鼠半舌切除缺损处可增加再生肌肉量,减少瘢痕挛缩,并可能增强有意义的舌功能。

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