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分泌型益生菌因子可改善锌缺乏的人源Caco-2和T84细胞系中的肠道致病菌感染。

Secreted probiotic factors ameliorate enteropathogenic infection in zinc-deficient human Caco-2 and T84 cell lines.

作者信息

Broekaert Ilse J, Nanthakumar N Nanda, Walker W Allan

机构信息

Department of Pediatrics, Mucosal Immunology and Developmental Gastroenterology Laboratories, Massachusetts General Hospital for Children, Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

Pediatr Res. 2007 Aug;62(2):139-44. doi: 10.1203/PDR.0b013e31809fd85e.

Abstract

Zinc deficiency enhances infectious diarrhea whereas probiotics may inhibit pathogen enterocyte invasion. The effect of probiotics on zinc-deficient versus normal human intestinal epithelium (Caco-2 and T-84) with regard to invasion and subsequent inflammatory response by Salmonella typhimurium was determined. Cells were infected with pathogens and preincubated with media conditioned by several lactobacilli or Bifidobacterium bifidum 12. Pathogen invasion was quantified, inflammation was determined by IL-8 secretion, and MAP kinase activation in the epithelium was analyzed. Probiotic inhibiting factors were partially characterized based on physicochemical properties. Zinc deficiency allowed for greater pathogen invasion and enhanced IL-8 secretion. Probiotic conditioned media reduced activation of proinflammatory signaling via the ERK and p38 pathway. Probiotic factors reverse increased susceptibility of zinc-deficient enterocytes to S. typhimurium invasion, suggesting an additive protective effect of probiotics in zinc deficiency. Probiotic conditioned media but not bacteria inhibited pathogen invasion and IL-8 production in zinc deficient enterocytes. Probiotic inhibitory factors are stable to treatment with proteases, deoxyribonucleases (DNAses), ribonucleases (RNAse), strong acid, and heat.

摘要

锌缺乏会加重感染性腹泻,而益生菌可能会抑制病原体对肠上皮细胞的侵袭。研究了益生菌对缺锌和正常人类肠上皮细胞(Caco-2和T-84)的影响,以及鼠伤寒沙门氏菌的侵袭和随后的炎症反应。细胞被病原体感染,并与几种乳酸杆菌或双歧杆菌12预处理过的培养基一起预孵育。对病原体侵袭进行定量,通过白细胞介素-8分泌来确定炎症,并分析上皮细胞中的丝裂原活化蛋白激酶激活情况。基于物理化学性质对益生菌抑制因子进行了部分表征。锌缺乏会导致更大程度的病原体侵袭和白细胞介素-8分泌增加。益生菌预处理过的培养基通过细胞外调节蛋白激酶(ERK)和p38途径减少促炎信号的激活。益生菌因子可逆转缺锌肠上皮细胞对鼠伤寒沙门氏菌侵袭敏感性的增加,表明益生菌在锌缺乏状态下具有累加的保护作用。益生菌预处理过的培养基而非细菌可抑制缺锌肠上皮细胞中的病原体侵袭和白细胞介素-8的产生。益生菌抑制因子对蛋白酶、脱氧核糖核酸酶(DNase)、核糖核酸酶(RNAse)、强酸和热的处理具有稳定性。

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