State Key Laboratory of Livestock and Poultry Breeding, Ministry of Agriculture Key Laboratory of Animal Nutrition and Feed Science in South China, Guangdong Key Laboratory of Animal Breeding and Nutrition, Institute of Animal Science, Guangdong Academy of Agricultural Sciences, 1 Dafeng 1st Street, Guangzhou 510640, China; Department of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
State Key Laboratory of Livestock and Poultry Breeding, Ministry of Agriculture Key Laboratory of Animal Nutrition and Feed Science in South China, Guangdong Key Laboratory of Animal Breeding and Nutrition, Institute of Animal Science, Guangdong Academy of Agricultural Sciences, 1 Dafeng 1st Street, Guangzhou 510640, China.
Int Immunopharmacol. 2020 Apr;81:106029. doi: 10.1016/j.intimp.2019.106029. Epub 2019 Nov 19.
Arginine supplementation improves intestinal damage and intestinal immunity, but the underlying mechanism of the effects of arginine supplementation on intestinal SIgA secretion is largely unknown. Therefore, this study was conducted to investigate the underlying pathway on the effects of arginine supplementation in secretory IgA (SIgA) production in mice. The results showed that 0.4% arginine supplementation promoted (P < 0.05) SIgA production in intestinal lumina and IgA plasma cell numbers in the ileum of mouse. Arginine supplementation significantly increased (P < 0.05) cytokines expression in mouse ileal associated with T cell-dependent and T cell-independent pathways of SIgA induction, including IL-5, IL-6, IL-13, transforming growth factor (TGF-)β2, TGF-β3, TGF-βR2, a proliferation-inducing ligand (APRIL), B cell-activating factor (BAFF), vasoactive intestinal peptide (VIP) receptor, and retinal dehydrogenases. Further study showed that 0.4% arginine supplementation markly decreased (P < 0.05) bacterial loads in mouse mesenteric lymph nodes and increased bacterial invasion into the mouse ileal wall, while supplementation of antibiotic abrogated the influence of arginine supplementation on SIgA secretion. Therefore, these data suggest that arginine supplementation might promote SIgA secretion through cytokines and intestinal microbiota might play an important role in SIgA secretion by arginine supplementation in the mouse intestine.
精氨酸补充可改善肠道损伤和肠道免疫,但精氨酸补充对肠道分泌型免疫球蛋白 A(SIgA)分泌影响的潜在机制在很大程度上尚不清楚。因此,本研究旨在探讨精氨酸补充对小鼠肠道分泌型免疫球蛋白 A(SIgA)产生的潜在作用途径。结果表明,0.4%精氨酸补充可促进(P<0.05)小鼠肠道腔中 SIgA 的产生和回肠中 IgA 浆细胞数量。精氨酸补充可显著增加(P<0.05)与 T 细胞依赖性和 T 细胞非依赖性 SIgA 诱导途径相关的细胞因子在小鼠回肠中的表达,包括白细胞介素-5(IL-5)、白细胞介素-6(IL-6)、白细胞介素-13(IL-13)、转化生长因子-β2(TGF-β2)、转化生长因子-β3(TGF-β3)、转化生长因子-β受体 2(TGF-βR2)、增殖诱导配体(APRIL)、B 细胞激活因子(BAFF)、血管活性肠肽(VIP)受体和视网膜脱氢酶。进一步研究表明,0.4%精氨酸补充可显著降低(P<0.05)小鼠肠系膜淋巴结中的细菌负荷,并增加细菌侵入小鼠回肠壁,而抗生素补充可消除精氨酸补充对 SIgA 分泌的影响。因此,这些数据表明,精氨酸补充可能通过细胞因子促进 SIgA 分泌,肠道微生物群可能在精氨酸补充促进小鼠肠道 SIgA 分泌中发挥重要作用。