The immunoregulatory role of fish specific type II SOCS via inhibiting metaflammation in the gut-liver axis

IF 5.1 Q1 ENVIRONMENTAL SCIENCES
Junwei Shan , Guangxin Wang , Heng Li , Xuyang Zhao , Weidong Ye , Lian Su , Qingsong Zhu , Yuhang Liu , Yingyin Cheng , Wanting Zhang , Nan Wu , Xiao-Qin Xia
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引用次数: 7

Abstract

SOCS8, also known as CISHb, is a fish-specific type II SOCS. Because CISH binds to cytokine receptors and may inhibit STAT5 activation (a substrate of the insulin receptor), SOCS8 may be involved in the control of metaflammation. The socs8−/− zebrafish were created, and both longer trunks and intestinal villi were observed in 1-month-old (mo) fish. Altered mucosal immunity and gut-liver metabolism were also found in socs8−/− fish. Increased intestinal neutrophils and macrophages, together with overexpression of cytokines and T cell markers in this mutant fish, suggested SOCS8's immunoregulating role. During modeling of soybean-induced enteritis using the 3 ​mo zebrafish, lower expression levels of inflammatory genes but more mucosa barrier disruption were discovered in socs8−/− zebrafish, compared with wide type counterparts. Furthermore, the shrunk villi at 6 ​mo in socs8−/− fish suggested that the mucosa might have been protected by SOCS8. This is also consistent with the assertion that metaflammation eventually leads to tissue degeneration and premature death. The fact that socs8−/− fish had more hepatic oil droplets compared to their wild-type counterparts suggested SOCS8's role in inhibiting hepatic metaflammation. Transcriptomic analysis as well as 16S rRNA gene sequencing were done on 3 ​mo socs8−/− fish to methodically reveal the altered immunity and metabolic reprogramming in the gut and liver caused by socs8−/−. The enriched GO terms for the intestinal tract, such as "cytokine-mediated signaling pathway" and "response to external biotic stimulus", as well as KEGG pathways in both gut and liver like "carbon metabolism" and "glycolysis/gluconeogenesis", were consistent with previously revealed pathological clues and improved growth performance at early age, respectively. In addition, the microbiota in the socs8−/− strain had adapted to the host's increased carbohydrate metabolism, as evidenced by higher levels of Bacteroidota. Furthermore, Verrucomicrobiota associated with immunoregulation were found in lower abundance in socs8−/− fish. As a result, current findings indicate that SOCS8 plays immunoregulatory and mucosa-protective roles in the fish gut and liver by inhibiting carbohydrate metabolism.

鱼类特异性II型SOCS通过抑制肠-肝轴上的超炎症的免疫调节作用
SOCS8,也称为CISHb,是一种鱼类特异性的II型SOCS。由于CISH与细胞因子受体结合,并可能抑制STAT5的激活(胰岛素受体的底物),SOCS8可能参与控制后炎症。创造了socs8−/−斑马鱼,在1个月大的(mo)鱼身上观察到了更长的躯干和肠绒毛。socs8−/−鱼的粘膜免疫和肠肝代谢也发生了改变。在这种突变鱼中,肠道中性粒细胞和巨噬细胞的增加,以及细胞因子和T细胞标志物的过度表达,表明SOCS8的免疫调节作用。在用3​mo斑马鱼,与宽型斑马鱼相比,socs8-/-斑马鱼的炎症基因表达水平较低,但粘膜屏障破坏较多。此外,6岁时绒毛收缩​socs8−/−fish中的mo表明粘膜可能受到socs8的保护。这也与后炎症最终导致组织退化和过早死亡的说法一致。与野生型鱼类相比,socs8−/-鱼类具有更多的肝油滴,这一事实表明socs8在抑制肝脏后炎症中的作用。转录组学分析和16S rRNA基因测序在3​mo socs8−/−鱼,系统地揭示socs8–/−引起的肠道和肝脏免疫和代谢重编程的改变。肠道的富集GO术语,如“细胞因子介导的信号通路”和“对外部生物刺激的反应”,以及肠道和肝脏中的KEGG通路,如“碳代谢”和“糖酵解/糖异生”,分别与先前揭示的病理线索和早期生长性能的改善相一致。此外,socs8−/−菌株中的微生物群已经适应了宿主增加的碳水化合物代谢,更高水平的拟杆菌证明了这一点。此外,在socs8−/−鱼类中发现了与免疫调节相关的Verrucomicobiota的丰度较低。因此,目前的研究结果表明,SOCS8通过抑制碳水化合物代谢,在鱼类肠道和肝脏中发挥免疫调节和粘膜保护作用。
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