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骨髓基质细胞移植对受损大鼠嗅黏膜的植入及再生作用

Engraftment and regenerative effects of bone marrow stromal cell transplantation on damaged rat olfactory mucosa.

作者信息

Kwon Jang-Woo, Jo Hyo Gyeong, Park Sang Man, Ku Cheol Hyo, Park Dong-Joon

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Yonsei University Wonju College of Medicine, 20 Ilsan-ro, Wonju, Gangwon, 220-701, Republic of Korea.

出版信息

Eur Arch Otorhinolaryngol. 2016 Sep;273(9):2585-90. doi: 10.1007/s00405-016-3957-x. Epub 2016 Mar 3.

Abstract

To develop a new therapeutic method to treat olfactory deficits, we investigated the engraftment and regenerative effects of transplanted bone marrow stromal cells (BMSCs) on damaged rat olfactory mucosa. To induce olfactory nerve degeneration, one side of the olfactory mucosa of Sprague-Dawley rats was damaged via Triton X-100 irrigation. Phosphate-buffered saline containing syngeneic BMSCs was injected into the olfactory mucosa for transplantation. PKH fluorescent cell dye labeling of BMSCs was used to monitor the transplanted cells. After transplantation of BMSCs, the thickness and regeneration of olfactory mucosa were analyzed using hematoxylin-eosin (H&E) staining. S100 immunohistochemical staining was used to measure nerve sheath regeneration. The increase in NGF (nerve growth factor) level in the olfactory mucosa was measured by Western blot analysis. Transplanted bone marrow stromal cells were engrafted to the lamia propria of damaged mucosa. The mean time for normalization of thickness and morphological recovery of the olfactory mucosa was 4 weeks in the therapeutic group and 9 weeks in the control group. S100 immunoreactivity was higher on the BMSC-treated side than on the control side. During regeneration, the expression of NGF increased in the olfactory mucosa of the experimental group. Based on these results, BMSC transplantation accelerated regeneration of olfactory mucosa damaged by Triton X-100, and NGF may be essential to this regenerative process.

摘要

为开发一种治疗嗅觉缺陷的新疗法,我们研究了移植的骨髓基质细胞(BMSCs)对受损大鼠嗅觉黏膜的植入和再生作用。为诱导嗅神经退变,通过用Triton X - 100冲洗,损伤Sprague - Dawley大鼠一侧的嗅觉黏膜。将含有同基因BMSCs的磷酸盐缓冲盐水注入嗅觉黏膜进行移植。使用PKH荧光细胞染料标记BMSCs来监测移植细胞。BMSCs移植后,采用苏木精 - 伊红(H&E)染色分析嗅觉黏膜的厚度和再生情况。用S100免疫组织化学染色来测量神经鞘再生。通过蛋白质印迹分析测量嗅觉黏膜中神经生长因子(NGF)水平的升高。移植的骨髓基质细胞植入受损黏膜的固有层。治疗组嗅觉黏膜厚度恢复正常和形态恢复的平均时间为4周,而对照组为9周。S100免疫反应性在BMSC治疗侧高于对照侧。在再生过程中,实验组嗅觉黏膜中NGF的表达增加。基于这些结果,BMSC移植加速了由Triton X - 100损伤的嗅觉黏膜的再生,并且NGF可能对该再生过程至关重要。

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