细胞外 Hsp70 参与了原代人类鼻腔上皮细胞的 CXCL12/CXCR4 通路:初步研究

Seong-Hee Kim, Dong Young Kahng, Kyung Soo Kim, H. Min
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引用次数: 0

摘要

背景与目的:迄今为止,还没有关于上呼吸道细胞外热休克蛋白70(Hsp70)和C-X-C趋化因子受体4型(CXCR4)之间相互作用的研究。我们的目的是评估细胞外热休克蛋白 70 和 CXCR4 之间的关系及其在原代人鼻上皮细胞中的作用:我们在空气-液体界面中培养了原代人鼻上皮细胞(HNE)。宏源公司进行了单细胞定量聚合酶链反应和测序。我们对CXCR4和丝裂原活化蛋白激酶(MAPK)通路进行了Western印迹分析:结果:细胞外 Hsp70 处理显著提高了原代 HNE 细胞中 CXCR4 的基因表达和蛋白水平。Hsp70和CXCL12共处理可增加磷酸ERK的表达,但CXCR4抑制剂AMD3100的预处理可抑制磷酸ERK的表达。用抗 Hsp70 抗体预处理可减少 Hsp70 和 CXCL12 共处理引起的磷酸-ERK 表达上调:结论:细胞外 Hsp70 参与激活了 HNE 细胞中依赖于 CXCR4 的下游信号通路。进一步的研究应评估细胞外 Hsp70-CXCL12/CXCR4 轴及其成分在炎症性疾病发展中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extracellular Hsp70 Is Involved in the CXCL12/CXCR4 Pathway in Primary Human Nasal Epithelial Cells: A Preliminary Study
Background and Objectives: To date, no studies have been conducted on the interaction between extracellular heat shock protein 70 (Hsp70) and C-X-C chemokine receptor type 4 (CXCR4) in the upper airway. We aimed to evaluate the relationship between extracellular Hsp70 and CXCR4 and their role in the primary human nasal epithelium.Methods: We cultured primary human nasal epithelial (HNE) cells in an air–liquid interface. Macrogen performed single-cell quantitative polymerase chain reaction and sequencing. We conducted western blot analysis for the CXCR4 and mitogen-activated protein kinase (MAPK) pathways.Results: Extracellular Hsp70 treatment significantly increased the genetic expression and protein levels of CXCR4 in primary HNE cells. Phospho-ERK expression was increased by cotreatment with Hsp70 and CXCL12, but inhibited by pretreatment with AMD3100, a CXCR4 inhibitor. Pretreatment with an anti-Hsp70 antibody reduced phospho-ERK expression upregulation induced by cotreatment with Hsp70 and CXCL12.Conclusion: Extracellular Hsp70 participates in the activation of the CXCR4-dependent downstream signaling pathway in HNE cells. Further studies should evaluate the extracellular Hsp70-CXCL12/CXCR4 axis and the role of its components in the development of inflammatory diseases.
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