Ito Koyu, Nakajima Akira, Fukushima Yuji, Suzuki Keiichiro, Sakamoto Keiko, Hamazaki Yoko, Ogasawara Kouetsu, Minato Nagahiro, Hattori Masakazu
Center for Innovation in Immunoregulative Technology and Therapeutics, Graduate School of Medicine, Kyoto University, Yoshida Konoe-cho, Sakyo-ku, Kyoto, Japan.
Department of Immunobiology, Institute of Development, Ageing, and Cancer, Tohoku University, Aoba-ku, Sendai, Miyagi, Japan.
PLoS One. 2017 Mar 15;12(3):e0173629. doi: 10.1371/journal.pone.0173629. eCollection 2017.
Osteopontin (Opn), a multifunctional extracellular matrix protein, is implicated in the pathogenesis of various inflammatory disorders. Under physiologic conditions, its expression is restricted to certain tissues including bone and kidney tubule. However, cellular activation during disease development induces Opn expression in various immune cells. In this study, using Opn-EGFP knock-in (KI) mice we found that CD8α+ T cells in the intestinal tissues, including Peyer's patch, lamina propria and epithelium, express Opn under steady state conditions. Therefore, we examined the role of Opn-expressing CD8α+ T cells in intestinal homeostasis. Interestingly, Opn knockout (KO) mice had altered fecal microflora concordant with a reduction of TCRγδ+ intraepithelial lymphocytes (IELs). Consistent with this result, both treatment with anti-Opn blocking antibody and deficiency of Opn resulted in decreased survival of TCRγδ+ and TCRαβ+ IELs. This data suggests that a possibility that Opn may function as a survival factor for IELs in the intestinal tissue. Collectively, these data suggest the possibility that Opn might regulate the homeostasis of intestinal microflora through maintenance of TCRγδ+ IELs, possibly by support of IEL survival.
骨桥蛋白(Opn)是一种多功能细胞外基质蛋白,与多种炎症性疾病的发病机制有关。在生理条件下,其表达仅限于某些组织,包括骨骼和肾小管。然而,疾病发展过程中的细胞激活会诱导多种免疫细胞表达Opn。在本研究中,我们使用Opn-EGFP基因敲入(KI)小鼠发现,在稳态条件下,包括派尔集合淋巴结、固有层和上皮在内的肠道组织中的CD8α+ T细胞表达Opn。因此,我们研究了表达Opn的CD8α+ T细胞在肠道稳态中的作用。有趣的是,Opn基因敲除(KO)小鼠的粪便微生物群发生了改变,同时TCRγδ+上皮内淋巴细胞(IEL)减少。与这一结果一致,抗Opn阻断抗体治疗和Opn缺乏均导致TCRγδ+和TCRαβ+ IEL的存活率降低。这些数据表明,Opn可能作为肠道组织中IEL的存活因子。总体而言,这些数据表明Opn可能通过维持TCRγδ+ IEL来调节肠道微生物群的稳态,可能是通过支持IEL的存活来实现的。