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低变应原婴儿配方奶粉缺乏转化生长因子-β活性,且抗炎活性低于普通婴儿配方奶粉。

Hypoallergenic infant formula lacks transforming growth factor beta activity and has a lower anti-inflammatory activity than regular infant formula.

机构信息

Department of Oral Biology, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria.

Department of Oral Biology, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria; Department of Periodontology, School of Dental Medicine, University of Bern, Freiburgstrasse 7, 3010 Bern, Switzerland; Austrian Cluster for Tissue Regeneration, Donaueschingenstraße 13, 1200 Vienna, Austria.

出版信息

J Dairy Sci. 2020 Aug;103(8):6771-6781. doi: 10.3168/jds.2019-18067. Epub 2020 Jun 3.

Abstract

Hypoallergenic formulas are recommended for infants who are not breastfed and cannot tolerate cow milk formulas due to allergy. These formulas are hydrolyzed to break down larger protein chains into shorter, easy-to-digest, and potentially less allergenic proteins. Hydrolysis, however, possibly occurs at the expense of the transforming growth factor beta (TGF-β) and anti-inflammatory activity that is inherent in regular formula. Our objective was to determine the TGF-β and the anti-inflammatory activity of commercially available hypoallergenic and regular formulas. Human gingival fibroblasts were incubated with reconstituted formulas followed by detection of TGF-β target genes and activation of Smad2/3 signaling. Gingival fibroblasts and the oral squamous cell carcinoma cell line HSC-2 were also exposed to formulas before adding interleukin (IL)1β and tumor necrosis factor (TNF)α to provoke expression of pro-inflammatory cytokines. For murine bone marrow-derived macrophages, pro-inflammatory cytokine expression was stimulated with saliva. Changes in p65 nuclear translocation and phosphorylation of smad3 and p38 were analyzed by immunostaining. Our study demonstrated that regular formula, but not hypoallergenic formula, enhanced the expression of TGF-β target genes IL11, PRG4, and NOX4 in gingival fibroblasts. Hypoallergenic formulas also failed to initiate nuclear translocation of Smad2/3 and phosphorylation of Smad3. Moreover, regular formulas were more potent than hypoallergenic formulas in reducing the expression of pro-inflammatory cytokines in gingival fibroblasts, HSC-2 epithelial cells, and murine bone marrow macrophages. Hypoallergenic and regular formulas had a similar capacity to reduce p65 nuclear translocation and phosphorylation of p38 in fibroblasts. These findings suggest that hypoallergenic formulas lack in vitro TGF-β activity and have a lower anti-inflammatory activity compared with regular formulas.

摘要

低敏配方适用于未母乳喂养且对牛奶配方过敏的婴儿。这些配方通过水解作用将较大的蛋白质链分解成较短的、易消化的、潜在低致敏性的蛋白质。然而,水解作用可能会以牺牲转化生长因子-β(TGF-β)和固有抗炎活性为代价。我们的目的是确定市售低敏配方和常规配方的 TGF-β 和抗炎活性。用人牙龈成纤维细胞孵育重建的配方,然后检测 TGF-β 靶基因和 Smad2/3 信号的激活。在添加白细胞介素(IL)1β和肿瘤坏死因子(TNF)α以引发促炎细胞因子表达之前,也将牙龈成纤维细胞和口腔鳞状细胞癌细胞系 HSC-2 暴露于配方中。对于鼠骨髓来源的巨噬细胞,用唾液刺激促炎细胞因子表达。通过免疫染色分析 p65 核易位以及 smad3 和 p38 的磷酸化变化。我们的研究表明,常规配方而非低敏配方增强了牙龈成纤维细胞中 TGF-β 靶基因 IL11、PRG4 和 NOX4 的表达。低敏配方也未能引发 Smad2/3 的核易位和 Smad3 的磷酸化。此外,常规配方在降低牙龈成纤维细胞、HSC-2 上皮细胞和鼠骨髓巨噬细胞中促炎细胞因子的表达方面比低敏配方更有效。低敏配方和常规配方在降低成纤维细胞中 p65 核易位和 p38 磷酸化方面具有相似的能力。这些发现表明,低敏配方缺乏体外 TGF-β 活性,并且与常规配方相比抗炎活性较低。

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