Nagai Koichi, Arai Hideo, Okudera Michisato, Yamamura Takashi, Oki Hidero, Komiyama Kazuo
Department of Pathology, Nihon University School of Dentistry, Tokyo, Japan.
J Oral Pathol Med. 2014 May;43(5):378-87. doi: 10.1111/jop.12145. Epub 2013 Dec 20.
Acinar cell regeneration from tubular structures has been reported to occur in duct-deligated salivary glands. However, the detailed process of acinar cell regeneration has not been clarified. We have developed a mouse duct ligation model to clarify the mechanisms underlying acinar cell regeneration, and we analyzed the epidermal growth factor receptor (EGFR) and epidermal growth factor (EGF) ligands using the model. We studied these ligands expressions in the course of acinar cell regeneration using immunohistochemistry and RT-PCR methods. In the duct-ligated portion of the submandibular gland (SMG) that underwent atrophy, newly formed acinar cells were observed arising from the tubular structures after the release of the duct obstruction. The constitutive expression of EGFR was observed by immunohistochemistry in both the duct-ligated and duct-deligated animals as well as in normal controls. The EGFR phosphorylation detected on the tubular structures after duct ligation paralleled the acinar cell regeneration. RT-PCR showed an increase in the epiregulin and heparin-binding EGF levels from day 0 to day 3 after the release of the duct obstruction. The EGF level was increased only after day 7. In vitro, cultured cells isolated from ligated SMGs proliferated and produced EGF ligands following the addition of epiregulin to the culture medium. These findings suggest that the tubular structures localized in an atrophic gland are the source of acinar cell regeneration of the salivary gland. The induction of EGF ligands, in particular epiregulin, may play an important role in acinar cell regeneration in this model.
据报道,在导管结扎的唾液腺中会发生从管状结构再生腺泡细胞的情况。然而,腺泡细胞再生的详细过程尚未阐明。我们建立了一个小鼠导管结扎模型来阐明腺泡细胞再生的潜在机制,并使用该模型分析了表皮生长因子受体(EGFR)和表皮生长因子(EGF)配体。我们使用免疫组织化学和逆转录-聚合酶链反应(RT-PCR)方法研究了这些配体在腺泡细胞再生过程中的表达。在经历萎缩的下颌下腺(SMG)的导管结扎部分,在解除导管阻塞后,观察到从管状结构中产生了新形成的腺泡细胞。通过免疫组织化学在导管结扎和导管切除的动物以及正常对照中均观察到EGFR的组成性表达。导管结扎后在管状结构上检测到的EGFR磷酸化与腺泡细胞再生平行。RT-PCR显示,在解除导管阻塞后第0天到第3天,表皮调节素和肝素结合EGF水平升高。EGF水平仅在第7天后升高。在体外,从结扎的SMG中分离的培养细胞在向培养基中添加表皮调节素后增殖并产生EGF配体。这些发现表明,萎缩腺体内的管状结构是唾液腺腺泡细胞再生的来源。在该模型中,EGF配体的诱导,尤其是表皮调节素,可能在腺泡细胞再生中起重要作用。