Spermidine enhances Immunoglobulin A secretory capacity in rat salivary glands: An ex vivo study

IF 2.3 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Yuta Hosomi , Yuko Yamamoto , Ryuta Endo , Masahiro Sugimoto , Wakako Sakaguchi , Shinya Fuchida , Toshiya Morozumi , Juri Saruta , Keiichi Tsukinoki
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Abstract

Objectives

Salivary Immunoglobulin A (IgA) plays a crucial role in mucosal immunity. However, the mechanisms that regulate its production are unclear. Spermidine (SPD), a polyamine involved in various cellular functions, has been implicated in immune modulation. In this study, we investigated the presence of SPD in rat salivary glands and its potential role in enhancing production of IgA.

Methods

Male Wistar rats were fed a low-polyamine diet for eight weeks. Submandibular and parotid glands were harvested and metabolomic analysis was used to determine the SPD concentration, reverse transcription quantitative polymerase chain reaction (RT-qPCR) was used to evaluate gene expression related to polyamine metabolism and autophagy, enzyme-linked immunosorbent assay (ELISA) was used to quantify secretion of IgA, and immunohistochemistry was used to localize spermidine synthase (SRM).

Results

Metabolomic analysis revealed that the concentration of SPD was significantly higher in the submandibular gland than in the parotid gland. RT-qPCR revealed higher SRM and LC3b mRNA expression, and lower Rubicon expression in the submandibular gland. Ex vivo SPD supplementation significantly increased secretion of IgA from both glands. Immunohistochemistry confirmed strong SRM expression in the acinar and ductal cells of the submandibular gland.

Conclusions

These findings suggest that SPD is endogenously synthesized in rat salivary glands, particularly in the submandibular gland, and may enhance the ex vivo production capacity of IgA in salivary gland tissues. These results provide insights into the role of polyamines in mucosal immunity and suggest potential therapeutic applications of SPD in enhancing oral immune defense.
亚精胺增强大鼠唾液腺免疫球蛋白A分泌能力的离体研究
目的唾液免疫球蛋白A (IgA)在粘膜免疫中起重要作用。然而,调控其产生的机制尚不清楚。亚精胺(SPD)是一种参与多种细胞功能的多胺,与免疫调节有关。在这项研究中,我们研究了SPD在大鼠唾液腺中的存在及其在促进IgA产生中的潜在作用。方法采用低多胺饲料喂养Wistar大鼠8周。取下颌下腺和腮腺,用代谢组学分析测定SPD浓度,用逆转录定量聚合酶链反应(RT-qPCR)评估多胺代谢和自噬相关基因表达,用酶联免疫吸附试验(ELISA)定量IgA分泌,用免疫组织化学定位亚精胺合成酶(SRM)。结果代谢组学分析显示,SPD在颌下腺中的浓度明显高于腮腺。RT-qPCR结果显示,大鼠颌下腺SRM和LC3b mRNA表达升高,Rubicon表达降低。体外补充SPD显著增加了两个腺体的IgA分泌。免疫组化证实SRM在颌下腺腺泡细胞和导管细胞中表达强烈。结论SPD可在大鼠唾液腺(尤其是下颌骨腺)内源性合成,并可增强唾液腺组织体内IgA的生成能力。这些结果揭示了多胺在粘膜免疫中的作用,并提示SPD在增强口腔免疫防御方面的潜在治疗应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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