Liu Xia, Cui Ting, Li Yingying, Wang Yuting, Wang Qinghong, Li Xin, Bi Yang, Wei Xiaoping, Liu Lan, Li Tingyu, Chen Jie
Children's Nutrition Research Center, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, CSTC2009 CA5002, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children's Hospital of Chongqing Medical University, Chongqing 400014, P.R. China.
Institute of Pediatrics, Children's Hospital of Chongqing Medical University, Chongqing 400014, P.R. China.
PLoS One. 2014 Dec 11;9(12):e114934. doi: 10.1371/journal.pone.0114934. eCollection 2014.
Vitamin A is a critical micronutrient for regulating immunity in many organisms. Our previous study demonstrated that gestational or early-life vitamin A deficiency decreases the number of immune cells in offspring. The present study aims to test whether vitamin A supplementation can restore lymphocyte pools in vitamin A-deficient rats and thereby improve the function of their intestinal mucosa; furthermore, the study aimed to identify the best time frame for vitamin A supplementation. Vitamin A-deficient pregnant rats or their offspring were administered a low-dose of vitamin A daily for 7 days starting on gestational day 14 or postnatal day 1, day 14 or day 28. Serum retinol concentrations increased significantly in all four groups that received vitamin A supplementation, as determined by high-performance liquid chromatography. The intestinal levels of secretory immunoglobulin A and polymeric immunoglobulin receptor increased significantly with lipopolysaccharide challenge in the rats that received vitamin A supplementation starting on postnatal day 1. The rats in this group had higher numbers of CD8+ intestinal intraepithelial lymphocytes, CD11C+ dendritic cells in the Peyer's patches and CD4+CD25+ T cells in the spleen compared with the vitamin A-deficient rats; flow cytometric analysis also demonstrated that vitamin A supplementation decreased the number of B cells in the mesenteric lymph nodes. Additionally, vitamin A supplementation during late gestation increased the numbers of CD8+ intestinal intraepithelial lymphocytes and decreased the numbers of B lymphocytes in the mesenteric lymph nodes. However, no significant differences in lymphocyte levels were found between the rats in the other two vitamin A supplement groups and the vitamin A-deficient group. In conclusion, the best recovery of a subset of lymphocytes in the offspring of gestational vitamin A-deficient rats and the greatest improvement in the intestinal mucosal immune response are achieved when vitamin A supplementation occurs during the early postnatal period.
维生素A是许多生物体中调节免疫的关键微量营养素。我们之前的研究表明,孕期或生命早期维生素A缺乏会减少后代免疫细胞的数量。本研究旨在测试补充维生素A是否能恢复维生素A缺乏大鼠的淋巴细胞库,从而改善其肠黏膜功能;此外,该研究旨在确定补充维生素A的最佳时间范围。从妊娠第14天或出生后第1天、第14天或第28天开始,对维生素A缺乏的孕鼠或其后代每天给予低剂量维生素A,持续7天。通过高效液相色谱法测定,所有接受维生素A补充的四组大鼠血清视黄醇浓度均显著升高。在出生后第1天开始接受维生素A补充的大鼠中,脂多糖刺激后,肠道分泌型免疫球蛋白A和多聚免疫球蛋白受体水平显著升高。与维生素A缺乏大鼠相比,该组大鼠的CD8 + 肠道上皮内淋巴细胞、派尔集合淋巴结中的CD11C + 树突状细胞以及脾脏中的CD4 + CD25 + T细胞数量更多;流式细胞术分析还表明,补充维生素A减少了肠系膜淋巴结中B细胞的数量。此外,妊娠后期补充维生素A增加了CD8 + 肠道上皮内淋巴细胞的数量,并减少了肠系膜淋巴结中B淋巴细胞的数量。然而,其他两个维生素A补充组的大鼠与维生素A缺乏组之间在淋巴细胞水平上未发现显著差异。总之,当在出生后早期补充维生素A时,妊娠维生素A缺乏大鼠后代的一部分淋巴细胞能得到最佳恢复,并且肠黏膜免疫反应能得到最大改善。