融合蛋白 rFlaA:Betv1 通过 p38-MAPK 和 COX2 依赖性上皮细胞 PGE 分泌来调节树突状细胞反应。

The Fusion Protein rFlaA:Betv1 Modulates DC Responses by a p38-MAPK and COX2-Dependent Secretion of PGE from Epithelial Cells.

机构信息

Molecular Allergology, Paul-Ehrlich-Institut, 63225 Langen, Germany.

Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

出版信息

Cells. 2021 Dec 4;10(12):3415. doi: 10.3390/cells10123415.

Abstract

Developing new adjuvants/vaccines and better understanding their mode-of-action is an important task. To specifically improve birch pollen allergy treatment, we designed a fusion protein consisting of major birch pollen allergen Betv1 conjugated to the TLR5-ligand flagellin (rFlaA:Betv1). This study investigates the immune-modulatory effects of rFlaA:Betv1 on airway epithelial cells. LA-4 mouse lung epithelial cells were stimulated with rFlaA:Betv1 in the presence/absence of various inhibitors with cytokine- and chemokine secretion quantified by ELISA and activation of intracellular signaling cascades demonstrated by Western blot (WB). Either LA-4 cells or LA-4-derived supernatants were co-cultured with BALB/c bone marrow-derived myeloid dendritic cells (mDCs). Compared to equimolar amounts of flagellin and Betv1 provided as a mixture, rFlaA:Betv1 induced higher secretion of IL-6 and the chemokines CCL2 and CCL20 from LA-4 cells and a pronounced MAPK- and NFB-activation. Mechanistically, rFlaA:Betv1 was taken up more strongly and the induced cytokine production was inhibited by NFB-inhibitors, while ERK- and p38-MAPK-inhibitors only suppressed IL-6 and CCL2 secretion. In co-cultures of LA-4 cells with mDCs, rFlaA:Betv1-stimulated LA-4 cells p38-MAPK- and COX2-dependently secreted PGE, which modulated DC responses by suppressing pro-inflammatory IL-12 and TNF-α secretion. Taken together, these results contribute to our understanding of the mechanisms underlying the strong immune-modulatory effects of flagellin-containing fusion proteins.

摘要

开发新的佐剂/疫苗并更好地了解其作用机制是一项重要任务。为了专门改善桦树花粉过敏治疗,我们设计了一种融合蛋白,该融合蛋白由主要桦树花粉过敏原 Betv1 与 TLR5 配体鞭毛蛋白(rFlaA:Betv1)缀合而成。本研究调查了 rFlaA:Betv1 对气道上皮细胞的免疫调节作用。用 rFlaA:Betv1 刺激 LA-4 小鼠肺上皮细胞,同时存在/不存在各种抑制剂,通过 ELISA 定量细胞因子和趋化因子的分泌,并通过 Western blot(WB)显示细胞内信号转导级联的激活。将 LA-4 细胞或 LA-4 衍生的上清液与 BALB/c 骨髓来源的髓样树突状细胞(mDCs)共培养。与作为混合物提供的等量鞭毛蛋白和 Betv1 相比,rFlaA:Betv1 诱导 LA-4 细胞中更高水平的 IL-6 和趋化因子 CCL2 和 CCL20 的分泌,并明显激活 MAPK 和 NFB。从机制上讲,rFlaA:Betv1 的摄取更强,并且诱导的细胞因子产生被 NFB 抑制剂抑制,而 ERK 和 p38-MAPK 抑制剂仅抑制 IL-6 和 CCL2 的分泌。在 LA-4 细胞与 mDCs 的共培养物中,rFlaA:Betv1 刺激的 LA-4 细胞通过 p38-MAPK 和 COX2 依赖性地分泌 PGE,通过抑制促炎的 IL-12 和 TNF-α 分泌来调节 DC 反应。总之,这些结果有助于我们理解鞭毛蛋白融合蛋白的强大免疫调节作用的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b2f/8700022/255e246e2ae4/cells-10-03415-g001.jpg

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