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首页> 外文期刊>Frontiers in Pharmacology >Fusobacterium nucleatum Activates Endoplasmic Reticulum Stress to Promote Crohn’s Disease Development via the Upregulation of CARD3 Expression
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Fusobacterium nucleatum Activates Endoplasmic Reticulum Stress to Promote Crohn’s Disease Development via the Upregulation of CARD3 Expression

机译:<斜体>血栓核核心核酸骨膜 - 激活内质网胁迫,以促进CROHN疾病的发育 CARD3表达的上调

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There is increasing evidence that members of the gut microbiota, especially Fusobacterium nucleatum ( F. nucleatum ), are associated with Crohn’s disease (CD), but the specific mechanism by which F. nucleatum promotes CD development is unclear. Here, we first examined the abundance of F. nucleatum and its effects on CD disease activity and explored whether F. nucleatum aggravated intestinal inflammation and promoted intestinal mucosal barrier damage in vitro and in vivo . Our data showed that F. nucleatum was enriched in 41.21% of CD tissues from patients and was correlated with the clinical course, clinical activity, and refractory behavior of CD (P & 0.05). In addition, we found that F. nucleatum infection is involved in activating the endoplasmic reticulum stress (ERS) pathway during CD development to promote intestinal mucosal barrier destruction. Mechanistically, F. nucleatum targeted caspase activation and recruitment domain 3 (CARD3) to activate the ERS pathway and promote F. nucleatum -mediated mucosal barrier damage in vivo and in vitro . Thus, F. nucleatum coordinates a molecular network involving CARD3 and ERS to control the CD process. Measuring and targeting F. nucleatum and its associated pathways will provide valuable insight into the prevention and treatment of CD.
机译:越来越多的证据表明肠道微生物群,尤其是核酸睾丸(F.核心问题)的成员与克罗恩病(CD)有关,但F.核心促进CD发育的具体机制尚不清楚。在这里,我们首先检查了对核心核和其对CD疾病活动的影响,并探讨了核癌是否加重肠炎症并促进体外和体内肠道粘膜阻挡损伤。我们的数据显示,F.核核富含患者的41.21%CD组织,并与CD的临床过程,临床活动和难治性行为相关(P <0.05)。此外,我们发现F.核核感染涉及在CD开发期间激活内质网应激(ERS)途径,以促进肠道粘膜屏障破坏。机械地,F.核靶向靶标胱天冬酶活化和募集结构域3(CARD3),以激活ERS途径,促进体内和体外核心介导的粘膜粘附损伤。因此,F.核核心坐标涉及CARD3和ERS来控制CD过程的分子网络。测量和靶向F.核核和其相关途径将提供有价值的见解CD的预防和治疗。

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