Takahashi-Horiuchi Yuko, Sugiyama Kanji, Sakashita Hideaki, Amano Osamu
Division of Anatomy, Meikai University School of Dentistry.
Tohoku J Exp Med. 2008 Mar;214(3):221-30. doi: 10.1620/tjem.214.221.
Heat shock protein 27 (Hsp27) has been suggested to participate in the cell proliferation and differentiation during tissue development. In fact, we have demonstrated the transient occurrence of Hsp27 during the differentiation of salivary gland acinar cells in postnatal rats. The purpose of the present study is to explore the potential role of Hsp27 in the proliferation and differentiation of the acinar cells during regeneration of the salivary gland. Using the experimental regeneration model of the rat submandibular gland after the release of duct ligation, the spatio-temporal localization of Hsp27 was investigated in immunohistochemistry in regenerating acini. No epithelial cells were immunoreactive for Hsp27 immediately after unligation, but Hsp27-immunoreactive cells were observed in regenerating acini located at the end portion of survived ductal tissues on the third day after unligation. The number of Hsp27-immunoreactive cells in regenerating acini reached its peak on the 5th day after unligation, and started to decline on the 7th day. They were undetectable on the 14th day. Importantly, the increase in the number of Hsp27-immunoreactive cells was preceded by the decline in the cell proliferative activity, and Hsp27-immunoreactivity declined and disappeared in conjunction with the progression of acinar cell differentiation, as judged by the double-immunostaining for Hsp27 and proliferating cell nuclear antigen, a cell proliferation marker, or glycine-rich protein-alpha, a specific marker of differentiated acinar cells. All the findings suggest that Hsp27 is expressed with the transition from the cell proliferation to differentiation of the acinar precursor cells during the regenerating process.
热休克蛋白27(Hsp27)被认为参与组织发育过程中的细胞增殖和分化。事实上,我们已经证明Hsp27在出生后大鼠唾液腺腺泡细胞分化过程中短暂出现。本研究的目的是探讨Hsp27在唾液腺再生过程中腺泡细胞增殖和分化中的潜在作用。利用大鼠下颌下腺导管结扎松解后的实验性再生模型,通过免疫组织化学研究再生腺泡中Hsp27的时空定位。结扎松解后立即没有上皮细胞对Hsp27呈免疫反应,但在结扎后第三天,在存活导管组织末端的再生腺泡中观察到Hsp27免疫反应性细胞。再生腺泡中Hsp27免疫反应性细胞的数量在结扎后第5天达到峰值,并在第7天开始下降。在第14天检测不到它们。重要的是,Hsp27免疫反应性细胞数量的增加先于细胞增殖活性的下降,并且根据Hsp27与细胞增殖标志物增殖细胞核抗原或分化腺泡细胞的特异性标志物富含甘氨酸蛋白-α的双重免疫染色判断,Hsp27免疫反应性随着腺泡细胞分化的进展而下降并消失。所有这些发现表明,在再生过程中,Hsp27随着腺泡前体细胞从细胞增殖向分化的转变而表达。