Veterinary Medicine College of Inner Mongolia Agricultural University, Hohhot 010018, China; Ministry of Agriculture, Key Laboratory of Clinical Diagnosis and Treatment Technology in Animal Disease, Hohhot 010018, China.
Veterinary Medicine College of Inner Mongolia Agricultural University, Hohhot 010018, China; Ministry of Agriculture, Key Laboratory of Clinical Diagnosis and Treatment Technology in Animal Disease, Hohhot 010018, China..
Cell Signal. 2019 Jan;53:304-315. doi: 10.1016/j.cellsig.2018.10.018. Epub 2018 Oct 26.
The ruminal mucosal epithelium can secrete defensins, which play a key role in innate and adaptive immunity and are considered potential replacements for antibiotics. Of these, sheep β-defensin-1 (SBD-1) is one of the most potent molecules produced by ovine ruminal epithelial cells (ORECs). β-glucan, safe and effective immune activators, can stimulate innate and adaptive immune responses. Here we examined whether β-glucan from Saccharomyces cerevisiae can induce SBD-1 expression in ORECs, as well as the underlying mechanism. First, ORECs were cultured, and quantitative real-time PCR (qPCR) and enzyme-linked immunosorbent assay (ELISA) were used to study the effects of different β-glucan concentrations. Then western blotting, immunohistochemistry, and immunocytofluorescence were performed to investigate the regulatory mechanism of β-glucan-induced SBD-1 upregulation. We show that β-glucan can induce the release of SBD-1 from ORECs; the highest SBD-1 mRNA and protein expression was achieved after treatment with 10 μg/mL at 2 and 4 h. Moreover, β-glucan-induced SBD-1 production was mediated by the activation of dendritic-cell-associated C-type lectin 1 (Dectin-1) receptors, Syk, and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB). These findings highlight the immunomodulatory effects of β-glucan on ORECs.
瘤胃黏膜上皮可以分泌防御素,防御素在先天和适应性免疫中起关键作用,被认为是抗生素的潜在替代品。在这些防御素中,绵羊β-防御素-1(SBD-1)是由绵羊瘤胃上皮细胞(ORECs)产生的最有效分子之一。β-葡聚糖是一种安全有效的免疫激活剂,能够刺激先天和适应性免疫反应。在这里,我们研究了酿酒酵母的β-葡聚糖是否能诱导 ORECs 表达 SBD-1,以及潜在的机制。首先,培养 ORECs,并用定量实时 PCR(qPCR)和酶联免疫吸附测定(ELISA)来研究不同β-葡聚糖浓度的影响。然后,通过western blot、免疫组织化学和免疫细胞荧光来研究β-葡聚糖诱导 SBD-1 上调的调节机制。我们发现β-葡聚糖可以诱导 ORECs 释放 SBD-1;在用 10μg/ml 的β-葡聚糖处理 2 和 4 小时后,SBD-1 的 mRNA 和蛋白表达最高。此外,β-葡聚糖诱导 SBD-1 的产生是通过树突状细胞相关 C 型凝集素 1(Dectin-1)受体、Syk 和核因子κB 轻链增强子的激活来介导的。这些发现强调了β-葡聚糖对 ORECs 的免疫调节作用。