Increased leptin response and inhibition of apoptosis in thymocytes of young rats offspring from protein deprived dams during lactation

PLoS One. 2013 May 10;8(5):e64220. doi: 10.1371/journal.pone.0064220. Print 2013.

Abstract

We investigated the consequences of mild maternal malnutrition in rat dams, in terms of thymocyte responses and the putative role of leptin. The young progeny of dams submitted to protein deprivation (PD) during lactation showed at 30 days of age lower body and thymus weights, significant alterations in CD4/CD8-defined T cell subsets without modifications in total thymocyte number as well as in proliferative response. Despite, the rats from PD group did not present alterations in leptin circulating levels, the expression of leptin receptor ObRb was enhanced in their thymocytes. This change was accompanied by an increase in leptin signaling response of thymocytes from PD rats, with an increase in JAK2 and STAT3 phosphorylation after leptin stimulation. Thymocytes from PD rats also presented a decreased rate of spontaneous apoptosis when compared to controls. Accordingly, higher expression of anti-apoptotic protein Bcl-2, and lower of pro-apoptotic protein Bax, with no change of pro-apoptotic Bad, and higher pro-caspase 3 content were detected in PD thymocytes. Moreover, thymocytes from PD group exhibited a constitutive higher nuclear content of p65 NF-kB associated to a lower IkB content in the cytoplasm. Finally, although there was no change in ob gene expression in PD thymocytes, a higher mRNA expression for the Ob gene was observed in the thymic microenvironment from PD animals. Taken together, the results show that mild maternal protein deprivation during lactation affects thymic homeostasis, enhancing leptin activity, which in turn protects thymocytes from apoptosis in the young progeny, with possible consequences upon the immune response of these animals in adult life.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins / metabolism
  • Apoptosis*
  • Body Weight
  • Cellular Microenvironment / genetics
  • Cellular Microenvironment / immunology
  • Diet, Protein-Restricted
  • Female
  • Gene Expression Regulation
  • Immunophenotyping
  • Janus Kinase 2 / metabolism
  • Lactation*
  • Leptin / blood
  • Leptin / genetics
  • Leptin / metabolism*
  • Male
  • NF-kappa B / metabolism
  • Protein-Energy Malnutrition*
  • Rats
  • Receptors, Leptin / metabolism
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • T-Lymphocyte Subsets / metabolism
  • Thymocytes / immunology
  • Thymocytes / metabolism*
  • Thymus Gland / cytology

Substances

  • Apoptosis Regulatory Proteins
  • Leptin
  • NF-kappa B
  • Receptors, Leptin
  • STAT3 Transcription Factor
  • Janus Kinase 2

Grants and funding

This study was funded by CAPES(www.capes.gov.br); CNPq (www.cnpq.br); FAPERJ (www.faperj.br). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.