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抗菌肽 LL-37 影响组织肥大细胞表面和细胞内 Toll 样受体的表达。

Cathelicidin LL-37 Affects Surface and Intracellular Toll-Like Receptor Expression in Tissue Mast Cells.

机构信息

Department of Experimental Immunology, Faculty of Health Sciences, Medical University of Lodz, Lodz, Poland.

Department of Molecular Cell Mechanisms, Faculty of Health Sciences, Medical University of Lodz, Lodz, Poland.

出版信息

J Immunol Res. 2018 Feb 19;2018:7357162. doi: 10.1155/2018/7357162. eCollection 2018.

Abstract

Undoubtedly, mast cells take part in host defense against microorganisms as they are numerous at the portal of infection, they release many proinflammatory and antimicrobial mediators, and they express pattern recognition receptors, such as TLRs. These receptors play a key role in recognition and binding molecules associated with microorganisms and molecules associated with damage. Cathelicidins exhibit direct antimicrobial activities against a broad spectrum of microbes by perturbing their cell membranes. Accumulating evidence suggests a role for these molecules in supporting cell activation. We examined the impact of human cathelicidin LL-37 on tissue mast cell TLR expression and distribution. Depending on context, we show that LL-37 stimulation resulted in minor to major effects on TLR2, TLR3, TLR4, TLR5, TLR7, and TLR9 expression. Confocal microscopy analysis showed that, upon stimulation, TLRs may translocate from the cell interior to the surface and conversely. FPR2 and EGFR inhibitors reduced the increase in expression of selected receptors. We also established that LL-37 acts as a powerful inducer of CCL3 and ROS generation. These results showed that in response to LL-37, mast cells enhance the capability to detect invading pathogens by modulation of TLR expression in what may be involved FPR2 or EGFR molecules.

摘要

毫无疑问,肥大细胞参与宿主对微生物的防御,因为它们在感染门户处数量众多,它们释放许多促炎和抗菌介质,并且它们表达模式识别受体,如 TLR。这些受体在识别和结合与微生物相关的分子以及与损伤相关的分子方面发挥着关键作用。Cathelicidins 通过扰乱其细胞膜对广谱微生物具有直接的抗菌活性。越来越多的证据表明这些分子在支持细胞激活方面发挥作用。我们研究了人源 cathelicidin LL-37 对组织肥大细胞 TLR 表达和分布的影响。根据具体情况,我们表明 LL-37 刺激对 TLR2、TLR3、TLR4、TLR5、TLR7 和 TLR9 的表达产生轻微至重大影响。共聚焦显微镜分析表明,刺激后 TLR 可能从细胞内部转移到表面,反之亦然。FPR2 和 EGFR 抑制剂减少了选定受体表达的增加。我们还确定 LL-37 是 CCL3 和 ROS 生成的强大诱导剂。这些结果表明,肥大细胞通过调节 TLR 表达来增强检测入侵病原体的能力,这可能涉及 FPR2 或 EGFR 分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52b8/5836302/37f7c04215d6/JIR2018-7357162.001.jpg

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