Saito Eri, Watari Ippei, Mizumachi-Kubono Mariko, Hsu-Hayashi Sumire, Ono Takashi
Department of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Front Physiol. 2020 Jun 10;11:528. doi: 10.3389/fphys.2020.00528. eCollection 2020.
Aquaporin 5 (AQP5) is a water channel-forming protein that plays a key role in saliva secretion. A decrease in masticatory function associated with the molar extraction adversely affects the submandibular salivary gland (SMG) in rats, inducing hypertrophic changes in the acinar cells and the expression of AQP5 in acinar cells or intercalated duct of the SMG. However, changes in AQP5 expression and localization in the SMG in association with occlusal modification have not been fully characterized.
We examined the influence of the decline and recovery of masticatory function on expression and localization of AQP5 in the rat SMG by inserting and removing an incisor bite plate (IBP). Thirty 5-week-old male Wistar rats were randomly divided into IBP ( = 12), recovery (REC) ( = 6), and control (CON) ( = 12) groups. Each rat in both the IBP and REC groups was fitted with the IBP on its maxillary incisors. Rats without the IBPs served as controls. All rats were fed powder diet and water . Rats in the IBP and CON groups were sacrificed after 14 ( = 6) and 28 ( = 6) days after the IBP attachment. In the REC group, the IBP was detached on the 14th day and sacrificed on 28th day after the IBP attachment. mRNA expression was quantified by reverse transcription-polymerase chain reaction. Changes in the localization of AQP5 were tracked by immunohistochemical staining.
Attachment of IBP resulted in a decrease in the expression of AQP5 in the IBP group. Changes in the localization of AQP5 were observed between 14 and 28 days in the IBP group. In contrast, changes in the expression and localization of AQP5 were not observed in the REC group.
Findings suggested that a loss of molar occlusion, due to the IBP attachment, altered AQP5 expression and localization in the rat SMG. However, removal of the bite plate allowed the recovery of both AQP5 expression and its normal localization in the SMGs.
水通道蛋白5(AQP5)是一种形成水通道的蛋白质,在唾液分泌中起关键作用。与磨牙拔除相关的咀嚼功能下降对大鼠下颌下唾液腺(SMG)产生不利影响,诱导腺泡细胞肥大性改变以及SMG腺泡细胞或闰管中AQP5的表达变化。然而,与咬合改变相关的SMG中AQP5表达和定位的变化尚未完全明确。
我们通过插入和移除门牙咬板(IBP)来研究咀嚼功能下降和恢复对大鼠SMG中AQP5表达和定位的影响。将30只5周龄雄性Wistar大鼠随机分为IBP组(n = 12)、恢复组(REC)(n = 6)和对照组(CON)(n = 12)。IBP组和REC组的每只大鼠上颌门牙均安装IBP。未安装IBP的大鼠作为对照。所有大鼠喂食粉末饲料并饮水。IBP组和CON组的大鼠在安装IBP后14天(n = 6)和28天(n = 6)处死。在REC组,IBP在第14天拆除,并在安装IBP后第28天处死。通过逆转录-聚合酶链反应定量mRNA表达。通过免疫组织化学染色追踪AQP5定位的变化。
IBP组中,安装IBP导致AQP5表达下降。在IBP组中,14至28天观察到AQP5定位的变化。相比之下,REC组未观察到AQP5表达和定位的变化。
研究结果表明,由于安装IBP导致磨牙咬合丧失,改变了大鼠SMG中AQP5的表达和定位。然而,移除咬板可使SMG中AQP5表达及其正常定位恢复。