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红细胞刺激人肺成纤维细胞分泌白细胞介素-8。

Red blood cells stimulate human lung fibroblasts to secrete interleukin-8.

作者信息

Fredriksson K, Lundahl J, Palmberg L, Romberger D J, Liu X D, Rennard S I, Skold C M

机构信息

Department of Medicine, Division of Respiratory Medicine, Karolinska Hospital, Stockholm, Sweden.

出版信息

Inflammation. 2003 Apr;27(2):71-8. doi: 10.1023/a:1023274532456.

Abstract

Following lung injury, red blood cells (RBC) may interact with extracellular matrix (ECM). Fibroblasts, the resident cell in the ECM, have the capacity to produce and secrete a variety of mediators including interleukin-8 (IL-8). In the present study we hypothesized that RBC, or soluble factors released from them, may stimulate IL-8 production by fibroblasts. Fibroblasts were cultured in a three-dimensional collagen gel culture system in the presence or absence of RBC or conditioned medium from RBC (RBC-CM). IL-8 release from fibroblasts was significantly increased when cultured with RBC or RBC-CM and both tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) further stimulated this IL-8 secretion. The enhanced production of IL-8 within fibroblasts was accompanied by increased IL-8 mRNA expression. To evaluate whether RBC-fibroblast interaction may lead to recruitment of neutrophils, a functional migration assay was performed. RBC and RBC-CM, in the presence of IL-1beta and TNF-alpha, increased the transmigration of neutrophils. Our results indicate that RBC, when interacting with ECM, may participate in the recruitment of inflammatory cells by stimulating fibroblasts to secrete IL-8. This might be an important mechanism regulating tissue repair after injury.

摘要

肺损伤后,红细胞(RBC)可能与细胞外基质(ECM)相互作用。成纤维细胞是ECM中的驻留细胞,有能力产生和分泌多种介质,包括白细胞介素-8(IL-8)。在本研究中,我们假设RBC或其释放的可溶性因子可能刺激成纤维细胞产生IL-8。在存在或不存在RBC或RBC条件培养基(RBC-CM)的情况下,将成纤维细胞培养在三维胶原凝胶培养系统中。与RBC或RBC-CM一起培养时,成纤维细胞释放的IL-8显著增加,肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)均进一步刺激这种IL-8分泌。成纤维细胞内IL-8产生的增强伴随着IL-8 mRNA表达的增加。为了评估RBC与成纤维细胞的相互作用是否可能导致中性粒细胞的募集,进行了功能迁移试验。在IL-1β和TNF-α存在的情况下,RBC和RBC-CM增加了中性粒细胞的迁移。我们的结果表明,RBC在与ECM相互作用时,可能通过刺激成纤维细胞分泌IL-8参与炎症细胞的募集。这可能是调节损伤后组织修复的重要机制。

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