Woods Lucas T, Jasmer Kimberly J, Muñoz Forti Kevin, Kearns Alex, Weisman Gary A
Department of Biochemistry, University of Missouri, Columbia, MO, United States.
Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, United States.
Front Dent Med. 2025 Jul 8;6:1612522. doi: 10.3389/fdmed.2025.1612522. eCollection 2025.
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 (, 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.
干燥综合征(SjD)是一种全身性自身免疫性疾病,主要影响外分泌腺,其特征为口干、眼干,血清中存在抗SSA和/或抗SSB自身抗体,以及唾液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,并且患B细胞淋巴瘤的风险增加。由于目前SjD的治疗主要集中在口腔和眼部症状管理上,因此确定疾病起始因素和进展机制可能为SjD提供新的治疗思路。SjD的白细胞介素-14α转基因(IL-14αTG)小鼠模型概括了人类SjD的许多方面,包括进行性涎腺炎、唾液腺功能丧失和B细胞淋巴瘤的发生。我们利用免疫荧光、流式细胞术、批量RNA测序和空间转录组分析来鉴定IL-14αTG类干燥综合征小鼠和年龄匹配的C57BL/6小鼠对照的下颌下腺中的免疫细胞亚群和差异表达基因(DEG)。我们进一步将IL-14αTG小鼠中DEG的基因本体与SjD患者和健康志愿者的小唾液腺活检中鉴定的DEG进行比较。结果表明,与C57BL/6小鼠相比,IL-14αTG小鼠的涎腺炎显著增加,这与浸润下颌下腺的边缘区B细胞比例增加相关。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患者小唾液腺中富集的DEG本体有大量重叠。最后,我们在空间上解析了IL-14αTG唾液腺内DEG的表达和定位,这是SjD小鼠模型下颌下腺空间转录组数据集的首次发表。