Takahashi S, Kohgo T, Nakamura S, Arambawatta A K S, Domon T, Yamamoto T, Wakita M
Department of Oral Health Science, Hokkaido University Graduate School of Dental Medicine, Sapporo, 060-8586, Japan,
J Mol Histol. 2005 Jun;36(5):373-9. doi: 10.1007/s10735-005-9009-2. Epub 2005 Nov 9.
The present study aimed to clarify how myoepithelial cells behave during regeneration of an atrophied sublingual gland by investigating cell proliferation and ultrastructure. Atrophy of rat sublingual glands was induced by unilateral ligation of the excretory duct near the hilum with metal clips, which were then removed after one week of ligation for regeneration. The sublingual glands 0-14 days after unligation were examined with single immunohistochemistry for actin as a marker of myoepithelial cells, double immunohistochemistry for actin and proliferating cell nuclear antigen (PCNA) as a marker of proliferating cells, and transmission electron microscopy (TEM). The single immunohistochemistry and TEM showed that myoepithelial cells surrounded residual ducts in the atrophied glands and immature and mature acini in the regenerating glands. Although PCNA-positive myoepithelial cells were identified during regeneration, PCNA labeling indices of myoepithelial cells were low at all time points except at day 7. Ultrastructurally, myoepithelial cells showing bizarre shaped structures in the atrophy changed with maturation of differentiating acinar cells and appeared normal in the regenerated glands. There was no differentiation of the remaining duct cells to myoepithelial cells. These observations suggest that proliferation of myoepithelial cells and differentiation to myoepithelial cells do not commonly participate in the regeneration of atrophied sublingual glands and that the bizarre shaped myoepithelial cells in the atrophied sublingual glands recover the original shapes with acinar cell regeneration.
本研究旨在通过研究细胞增殖和超微结构,阐明肌上皮细胞在萎缩舌下腺再生过程中的行为。通过用金属夹在靠近肺门处单侧结扎排泄管来诱导大鼠舌下腺萎缩,结扎一周后移除金属夹以进行再生。对结扎后0 - 14天的舌下腺进行单免疫组化检测肌动蛋白作为肌上皮细胞的标志物,双免疫组化检测肌动蛋白和增殖细胞核抗原(PCNA)作为增殖细胞的标志物,以及透射电子显微镜(TEM)检测。单免疫组化和TEM显示,肌上皮细胞围绕萎缩腺体中的残留导管以及再生腺体中的未成熟和成熟腺泡。尽管在再生过程中鉴定出了PCNA阳性的肌上皮细胞,但除第7天外,肌上皮细胞的PCNA标记指数在所有时间点都很低。超微结构上,萎缩中呈现奇异形状结构的肌上皮细胞随着分化腺泡细胞的成熟而发生变化,在再生腺体中看起来正常。其余导管细胞未分化为肌上皮细胞。这些观察结果表明,肌上皮细胞的增殖和向肌上皮细胞的分化通常不参与萎缩舌下腺的再生,并且萎缩舌下腺中奇异形状的肌上皮细胞随着腺泡细胞再生恢复其原始形状。