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Brugia malayi 编码的白细胞介素 5 受体结合蛋白的定位和 RNA 干扰驱动抑制。

Localization and RNA Interference-Driven Inhibition of a Brugia malayi-Encoded Interleukin-5 Receptor Binding Protein.

机构信息

Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA.

Lindsay F. Kimball Research Institute, New York Blood Centergrid.250415.7, New York, New York, USA.

出版信息

Infect Immun. 2022 May 19;90(5):e0031721. doi: 10.1128/iai.00317-21. Epub 2022 Apr 25.

Abstract

A molecule we termed Brugia malayi IL-5 receptor (IL-5R) binding protein (BmIL5Rbp; also known as Bm8757) was identified from B. malayi filarial worms and found to inhibit human interleukin-5 (IL-5) binding to its human receptor competitively. After the expression and purification of a recombinant BmIL5Rbp and generation of BmIL5Rbp-specific rabbit antibody, we localized the molecule on B. malayi worms through immunohistochemistry and immunoelectron microscopy. RNA interference (RNAi) was used to inhibit BmIL5Rbp mRNA and protein production. BmIL5Rbp was shown to localize to the cuticle of Brugia malayi and to be released in its excretory/secretory products. RNAi inhibited BmIL5Rbp mRNA production by 33%, reduced the surface protein expression by ~50%, and suppressed the release of BmIL5Rbp in the excretory/secretory products. RNAi has been used successfully to knock down the mRNA and protein expression of BmIL5Rbp in the early larval stages of B. malayi and provided a proof of principle for the local inhibition of the human IL-5R. These findings provide evidence that a parasite-encoded IL-5R antagonist may locally inhibit a vital host innate immune activation of IL-5 on eosinophils.

摘要

我们从班氏丝虫中鉴定出一种名为班氏丝虫白细胞介素 5 受体(IL-5R)结合蛋白(BmIL5Rbp;也称为 Bm8757)的分子,它能竞争性地抑制人白细胞介素 5(IL-5)与其人类受体结合。在表达和纯化重组 BmIL5Rbp 并生成 BmIL5Rbp 特异性兔抗体后,我们通过免疫组织化学和免疫电子显微镜将该分子定位于班氏丝虫蠕虫上。通过 RNA 干扰(RNAi)抑制 BmIL5Rbp mRNA 和蛋白的产生。结果表明 BmIL5Rbp 定位于班氏丝虫的表皮,并在其排泄/分泌产物中释放。RNAi 抑制了 BmIL5Rbp mRNA 的产生 33%,降低了表面蛋白表达约 50%,并抑制了排泄/分泌产物中 BmIL5Rbp 的释放。RNAi 已成功用于敲低班氏丝虫早期幼虫阶段的 BmIL5Rbp mRNA 和蛋白的表达,并为局部抑制人类 IL-5R 提供了原理证明。这些发现为寄生虫编码的 IL-5R 拮抗剂可能局部抑制 IL-5 对嗜酸性粒细胞的重要宿主固有免疫激活提供了证据。

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