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短篇通讯:山羊乳腺中抗菌肽 S100A8 的产生及乳内注射脂多糖对奶中 S100A8 浓度的影响。

Short communication: Production of antimicrobial peptide S100A8 in the goat mammary gland and effect of intramammary infusion of lipopolysaccharide on S100A8 concentration in milk.

机构信息

Graduate School of Biosphere Science, Hiroshima University, Higashi-Hiroshima, 739-8528, Japan.

Graduate School of Biosphere Science, Hiroshima University, Higashi-Hiroshima, 739-8528, Japan.

出版信息

J Dairy Sci. 2019 May;102(5):4674-4681. doi: 10.3168/jds.2018-15396. Epub 2019 Mar 7.

Abstract

This study aimed to determine the production site of antimicrobial peptide S100A8 in the goat mammary gland and changes in its concentration in milk after lipopolysaccharide (LPS) challenge. Sixteen Tokara goats were used in this study for mammary gland tissue, blood leukocyte, and milk somatic cell collection and LPS challenge. The mRNA expression and protein localization of S100A8 in the mammary gland parenchyma and teat, blood leukocytes, and milk somatic cells were examined by reverse-transcription PCR and immunohistochemistry. The S100A8 concentration in milk was measured at 0 to 144 h after intramammary challenge of LPS by enzyme immunoassay. The mRNA of S100A8 was expressed in the parenchyma and teat, leukocytes isolated from blood, and milk somatic cells. Antimicrobial peptide S100A8 was immunolocalized in the outermost layer of the teat skin of udders with and without LPS infusion, whereas in the mammary gland it was immunolocalized only in the leukocytes infiltrated in the alveoli after LPS infusion. Antimicrobial peptide S100A8 was also immunolocalized in the blood and milk leukocytes. The number of S100A8-positive cells in milk was higher than that in blood. The concentration of S100A8 in milk increased significantly at 72 h after intramammary infusion of LPS. These results suggest that S100A8 is produced in the leukocytes and that its secretion into milk is affected by LPS stimulation.

摘要

本研究旨在确定山羊乳腺中抗菌肽 S100A8 的产生部位以及脂多糖(LPS)刺激后乳中其浓度的变化。本研究使用 16 只 Tokara 山羊进行乳腺组织、血白细胞和奶体细胞采集和 LPS 刺激。通过逆转录 PCR 和免疫组织化学检测 S100A8 在乳腺实质和乳头、血白细胞和奶体细胞中的 mRNA 表达和蛋白定位。通过酶联免疫吸附试验在 LPS 经乳腺内注入后 0 至 144 小时测量乳中 S100A8 的浓度。S100A8 的 mRNA 在实质和乳头、从血液中分离的白细胞和奶体细胞中表达。抗菌肽 S100A8 在有和没有 LPS 输注的乳头最外层皮肤中免疫定位,而在乳腺中仅在 LPS 输注后浸润在肺泡中的白细胞中免疫定位。抗菌肽 S100A8 也在血液和奶白细胞中免疫定位。奶中 S100A8 阳性细胞的数量高于血液。LPS 经乳腺内注入后 72 小时乳中 S100A8 的浓度显著增加。这些结果表明 S100A8 是由白细胞产生的,其分泌到乳中受到 LPS 刺激的影响。

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