Hovd Aud-Malin Karlsson, Nayar Saba, Smith Charlotte G, Kanapathippillai Premasany, Iannizzotto Valentina, Barone Francesca, Fenton Kristin Andreassen, Pedersen Hege Lynum
Department of Medical Biology, Faculty of Health Sciences, UiT The Arctic University of Norway, Tromsø, Norway.
Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom.
Front Immunol. 2024 Sep 17;15:1455238. doi: 10.3389/fimmu.2024.1455238. eCollection 2024.
Tertiary lymphoid structures (TLSs) are formed in tissues targeted by chronic inflammation processes, such as infection and autoimmunity. In Sjögren's disease, the organization of immune cells into TLS is an important part of disease progression. Here, we investigated the dynamics of tissue resident macrophages in the induction and expansion of salivary gland TLS. We induced Sjögren's disease by cannulation of the submandibular glands of C57BL/6J mice with LucAdV5. In salivary gland tissues from these mice, we analyzed the different macrophage populations prior to cannulation on day 0 and on day 2, 5, 8, 16 and 23 post-infection using multicolored flow cytometry, mRNA gene analysis, and histological evaluation of tissue specific macrophages. The histological localization of macrophages in the LucAdV5 induced inflamed salivary glands was compared to salivary glands of NZBW/F1 lupus prone mice, a spontaneous mouse model of Sjögren's disease. The evaluation of the dynamics and changes in macrophage phenotype revealed that the podoplanin (PDPN) expressing CX3CR1 macrophage population was increased in the salivary gland tissue during LucAdV5 induced inflammation. This PDPN CX3CR1 macrophage population was, together with PDPNCD206 macrophages, observed to be localized in the parenchyma during the acute inflammation phase as well as surrounding the TLS structure in the later stages of inflammation. This suggests a dual role of tissue resident macrophages, contributing to both proinflammatory and anti-inflammatory processes, as well as their possible interactions with other immune cells within the inflamed tissue. These macrophages may be involved with lymphoid neogenesis, which is associated with disease severity and progression. In conclusion, our study substantiates the involvement of proinflammatory and regulatory macrophages in autoimmune pathology and underlines the possible multifaceted functions of macrophages in lymphoid cell organization.
三级淋巴结构(TLSs)在慢性炎症过程(如感染和自身免疫)所靶向的组织中形成。在干燥综合征中,免疫细胞组织形成TLS是疾病进展的重要组成部分。在此,我们研究了组织驻留巨噬细胞在唾液腺TLS诱导和扩展中的动态变化。我们通过用LucAdV5插管C57BL/6J小鼠的下颌下腺来诱导干燥综合征。在这些小鼠的唾液腺组织中,我们在感染前的第0天以及感染后的第2、5、8、16和23天,使用多色流式细胞术、mRNA基因分析和组织特异性巨噬细胞的组织学评估,分析了不同的巨噬细胞群体。将LucAdV5诱导的炎症唾液腺中巨噬细胞的组织学定位与NZBW/F1狼疮易感小鼠(一种干燥综合征的自发小鼠模型)的唾液腺进行了比较。对巨噬细胞表型的动态变化和改变的评估显示,在LucAdV5诱导的炎症期间,唾液腺组织中表达血小板内皮细胞黏附分子(PDPN)的CX3CR1巨噬细胞群体增加。观察到这个PDPN⁺CX3CR1巨噬细胞群体与PDPN⁺CD206巨噬细胞一起,在急性炎症期定位于实质内,在炎症后期定位于TLS结构周围。这表明组织驻留巨噬细胞具有双重作用,既参与促炎过程也参与抗炎过程,以及它们在炎症组织内与其他免疫细胞可能的相互作用。这些巨噬细胞可能参与淋巴新生,而淋巴新生与疾病严重程度和进展相关。总之,我们的研究证实了促炎和调节性巨噬细胞参与自身免疫病理,并强调了巨噬细胞在淋巴细胞组织中可能具有的多方面功能。