Salivary gland transcriptomic analysis and immunophenotyping in the IL-14α transgenic mouse model of Sjögren's disease.

IF 1.5 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Frontiers in dental medicine Pub Date : 2025-07-08 eCollection Date: 2025-01-01 DOI:10.3389/fdmed.2025.1612522
Lucas T Woods, Kimberly J Jasmer, Kevin Muñoz Forti, Alex Kearns, Gary A Weisman
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引用次数: 0

Abstract

Sjögren's disease (SjD) is a systemic autoimmune disorder primarily affecting the exocrine glands and characterized by dry mouth and dry eye, the presence of anti-SSA and/or anti-SSB autoantibodies in blood serum, and chronic lymphocytic infiltration of salivary and lacrimal glands (i.e., sialadenitis and dacryoadenitis, respectively). In addition to reduced quality of life, SjD patients experience severe oral health complications and are at increased risk of developing B cell lymphoma. Because current SjD treatments primarily focus on oral and ocular symptom management, identifying initiating factors and mechanisms of disease progression may offer new therapeutic insights for SjD. The interleukin-14α transgenic (IL-14αTG) mouse model of SjD recapitulates many aspects of human SjD, including progressive sialadenitis, loss of salivary gland function, and development of B cell lymphoma. We utilized immunofluorescence, flow cytometry, bulk RNA sequencing and spatial transcriptomic analyses to identify immune cell subpopulations and differentially expressed genes (DEGs) in submandibular glands of IL-14αTG Sjögren's-like mice and age-matched C57BL/6 mouse controls. We further compared the gene ontology of DEGs in IL-14αTG mice to DEGs identified in minor salivary gland biopsies from SjD patients and healthy volunteers. Results demonstrated significantly increased sialadenitis in IL-14αTG compared to C57BL/6 mice that correlated with an increased proportion of marginal zone B cells infiltrating the submandibular gland. Whole transcriptome analyses showed substantial overlap in enriched DEG ontology between IL-14αTG mouse submandibular gland and SjD patient minor salivary gland, compared to C57BL/6 mice and healthy human volunteer controls, respectively. Lastly, we spatially resolved DEG expression and localization within IL-14αTG salivary glands, marking the first publication of a spatial transcriptomic dataset from submandibular glands in a SjD mouse model.

IL-14α转基因Sjögren病小鼠模型的唾液腺转录组学分析和免疫表型分析。
Sjögren's disease (SjD)是一种主要影响外分泌腺的系统性自身免疫性疾病,其特征是口干和眼干,血清中存在抗ssa和/或抗ssb自身抗体,以及涎腺和泪腺的慢性淋巴细胞浸润(分别为涎腺炎和泪腺炎)。除了生活质量下降外,SjD患者还会出现严重的口腔健康并发症,并增加患B细胞淋巴瘤的风险。由于目前的SjD治疗主要集中在口腔和眼部症状管理上,确定疾病进展的起始因素和机制可能为SjD的治疗提供新的见解。白细胞介素-14α转基因(IL-14αTG)小鼠SjD模型概括了人类SjD的许多方面,包括进行性涎腺炎、唾液腺功能丧失和B细胞淋巴瘤的发展。我们利用免疫荧光、流式细胞术、大量RNA测序和空间转录组学分析鉴定IL-14αTG Sjögren's样小鼠和年龄匹配的C57BL/6小鼠下颌骨腺免疫细胞亚群和差异表达基因(DEGs)。我们进一步比较了IL-14αTG小鼠中DEGs的基因本体与SjD患者和健康志愿者小涎腺活检中鉴定的DEGs。结果显示,与C57BL/6小鼠相比,IL-14αTG的涎腺炎明显增加,这与边缘带B细胞浸润下颌骨腺的比例增加有关。全转录组分析显示,与C57BL/6小鼠和健康人类志愿者对照相比,IL-14αTG小鼠下颌下腺和SjD患者小唾液腺在富集DEG本体上存在大量重叠。最后,我们在空间上解析了IL-14αTG唾液腺中DEG的表达和定位,这标志着SjD小鼠模型中颌下腺的空间转录组数据的首次发表。
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
CiteScore
2.10
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审稿时长
13 weeks
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