首页> 外文期刊>Differentiation: The Journal of the International Society of Differentiation >Regeneration of acinar cells following ligation of rat submandibular gland retraces the embryonic-perinatal pathway of cytodifferentiation.
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Regeneration of acinar cells following ligation of rat submandibular gland retraces the embryonic-perinatal pathway of cytodifferentiation.

机译:大鼠下颌下腺结扎后腺泡细胞的再生追溯了细胞分化的胚胎-围产期途径。

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Rat submandibular gland can regenerate following ligation-induced atrophy, eventually recovering its normal morphology and function. Previous studies have suggested that the regeneration process implies both self-proliferation of existing acini and formation of new acinar cells. One hypothesis is that new acinar cells may differentiate from the ductal cells in a similar fashion to the process of cytodifferentiation occurring during submandibular glandular development. In this study atrophy was induced, under recovery anaesthesia, by applying a metal clip on the main duct of the submandibular gland without including the chorda lingual nerve. After 2 weeks the duct was deligated for 3, 5 or 7 days or 8 weeks and the glands collected. Tissue was prepared for immunohistochemistry, biochemical analysis and RNA extraction. The histology of the regenerated glands shows several normal-looking acini, which have regained their glycoprotein content (AB/PAS positive), data also confirmed by biochemical analysis (SDS-PAGE/PAS). Regenerating tissue was characterized by the presence of embryonic-like branched structures ending with AB/PAS positive acinar cells. The proteins SMG-B and PSP are normally expressed in acinar cell precursors during development but only by intercalated ductal cells in the adult stage. In the adult regenerating gland mRNA levels of both SMG-B and PSP were found to be up-regulated compared to ligated glands and SMG-B expression localized to acinar cells whilst the ductal cells were negative. This study of rat submandibular gland regeneration suggests new acinar cells have differentiated from ducts and express markers of acinar cell precursors in a similar manner to the cytodifferentiation process occurring during glandular development.
机译:结扎引起的萎缩后,大鼠下颌下腺可再生,最终恢复其正常形态和功能。先前的研究表明,再生过程既意味着现有腺泡的自我增殖,又意味着新的腺泡细胞的形成。一种假设是,新的腺泡细胞可能以与下颌下腺发育过程中发生的细胞分化过程相似的方式与导管细胞分化。在这项研究中,在恢复麻醉下,通过在下颌下腺的主导管上应用金属夹而不包括脉络膜舌神经来诱发萎缩。 2周后,将导管结扎3、5、7天或8周,收集腺体。准备组织用于免疫组织化学,生化分析和RNA提取。再生腺的组织学表现为数个外观正常的腺泡,已恢复其糖蛋白含量(AB / PAS阳性),生化分析(SDS-PAGE / PAS)也证实了数据。再生组织的特征是存在以AB / PAS阳性腺泡细胞结尾的类胚胎分支结构。 SMG-B和PSP蛋白通常在发育过程中在腺泡细胞前体中表达,但仅在成年期由插入的导管细胞表达。与结扎的腺体相比,在成年的再生腺体中,SMG-B和PSP的mRNA水平均被上调,并且SMG-B的表达局限于腺泡细胞,而导管细胞为阴性。对大鼠下颌下腺再生的这项研究表明,新的腺泡细胞已从导管中分化出来,并以与腺体发育过程中发生的细胞分化过程相似的方式表达腺泡细胞前体的标志物。

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