| Literature DB >> 31959270 |
Jean-Baptiste Armengaud1, Zelie Dennebouy1, Danny Labes2, Catherine Fumey3, Anne Wilson2,3, Fabio Candotti4, Catherine Yzydorczyk1, Umberto Simeoni1.
Abstract
Early malnutrition, the first environmental cause of intra-uterine growth restriction, impairs development of the thymus. Alterations of the thymic structure and function are reported at young ages in murine and ovine models. However, descriptions of thymic consequences of fetal malnutrition at adulthood are scarce. The present study investigates thymic structure, protein expression and cell selection process observed at postnatal day 180 (PND180) in male offspring of rats exposed to maternal low-protein diet (mLPD) compared with control diet during gestation. The thymic index was lower in adult offspring exposed to mLPD (P < 0·05). The thymic cortico-medullar ratio was lower in adult offspring exposed to mLPD (P < 0·05). At PND180, the protein expression of the lymphotoxin β receptor (P < 0·05), the autoimmune regulator (P < 0·05) and Forkhead Box P3 (FoxP3; P < 0·05) was all significantly lower in the mLPD group. The CD4+:CD8+ single-positive thymocyte subpopulation ratio and CD4+:CD8+ lymphocyte subpopulation ratio were increased in the mLPD group (P < 0·05). Among CD3+ lymphocytes, the proportions of CD4+CD8+ double-positive lymphocytes, CD31+ recent thymic emigrants and CD4+FoxP3+ lymphocytes were not significantly different between mLPD and control groups. These findings suggest mLPD during gestation induced long-lasting alterations in the development of thymic structure and thymic cell maturation and selection process in adult male rat offspring.Entities:
Keywords: Developmental origins of health and disease; Early-life nutrition; Intra-uterine growth restriction; Nutritional immunology; Thymus
Mesh:
Year: 2020 PMID: 31959270 DOI: 10.1017/S000711452000015X
Source DB: PubMed Journal: Br J Nutr ISSN: 0007-1145 Impact factor: 3.718