Specific localization of fibroblasts at the intercalated duct in the major salivary glands of rats

IF 2.6 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Go Onozawa , Arata Nagasaka , Yasuhiko Bando , Koji Sakiyama , Nobuharu Yamamoto , Osamu Amano
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Abstract

Objectives

Immunohistochemical methods were employed to investigate the morphological heterogeneity and localization of fibroblasts associated with the function of major salivary glands in rats.

Methods

Histochemical and electron microscopic observations were made in rat parotid, submandibular, and sublingual glands and pancreas. Fibroblasts were immunostained using their specific marker, 47 kDa heat shock protein (Hsp47).

Results

Hsp47-immunopositive fibroblasts within the intralobular connective tissue exhibited a notably smaller size compared with the interlobular connective tissue. They were loosely distributed throughout the connective tissue. However, fibroblasts with elongated long processes were explicitly identified at the intercalated ducts in parotid, sublingual, and submandibular glands. Fibroblastic bodies and processes were tightly approximated with the basement membrane of the duct. Electron microscopy confirmed these findings, revealing a thin layer consisting of collagen fibers was found between the fibroblasts and the basement membrane. Double staining of Hsp47 and α-smooth muscle actin (αSMA) in parotid glands indicating that Hsp47-positive fibroblasts enveloped both the duct and αSMA-positive myoepithelial cells. Additionally, They projected long and thin processes longitudinally at the straight portion or circularly at the bifurcated portion of the duct. The three-dimensional reconstruction showed a frame-like structure of fibroblasts surrounding the intercalated duct with longitudinal myoepithelial cells. However, such specific localization of fibroblasts was not detected in the exocrine pancreas lacking myoepithelium.

Conclusions

Small fibroblasts with long processes connecting or overwrapping each other and thin collagen layers surround the intercalated ducts in rat major salivary glands, presumably contributing to protecting the ducts from salivary flow and myoepithelial contraction.

Abstract Image

成纤维细胞在大鼠主要唾液腺闰管处的特异性定位
目的:采用免疫组化方法研究与大鼠主要唾液腺功能相关的成纤维细胞的形态异质性和定位:方法:对大鼠腮腺、颌下腺、舌下腺和胰腺进行组织化学和电子显微镜观察。使用成纤维细胞的特异性标记物 47 kDa 热休克蛋白(Hsp47)对其进行免疫染色:结果:与小叶间结缔组织相比,小叶内结缔组织中 Hsp47 免疫阳性成纤维细胞的体积明显较小。它们松散地分布在整个结缔组织中。不过,在腮腺、舌下腺和颌下腺的闰导管中,可以清晰地发现带有细长突起的成纤维细胞。成纤维细胞体和过程与导管基底膜紧密贴合。电子显微镜证实了这些发现,显示在成纤维细胞和基底膜之间有一层由胶原纤维组成的薄层。腮腺中 Hsp47 和 α 平滑肌肌动蛋白(αSMA)的双重染色表明,Hsp47 阳性的成纤维细胞同时包裹着导管和 αSMA 阳性的肌上皮细胞。此外,它们还在导管的直线部分纵向或分叉部分环形伸出细长的突起。三维重建显示,成纤维细胞与纵向肌上皮细胞组成的框架结构围绕着插管。然而,在缺乏肌上皮细胞的外分泌胰腺中却未检测到成纤维细胞的这种特异性定位:结论:大鼠大唾液腺的闰导管周围环绕着小的成纤维细胞,这些成纤维细胞具有相互连接或包裹的长过程和薄胶原层,可能有助于保护闰导管免受唾液流和肌上皮收缩的影响。
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来源期刊
Journal of Oral Biosciences
Journal of Oral Biosciences DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.40
自引率
12.50%
发文量
57
审稿时长
37 days
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