Literature DB >> 28282643

Nab2 maintains thymus cellularity with aging and stress.

K Taraszka Hastings1, Diana Elizalde2, Leela Muppana2, Sarah Levine2, Christy M Kamel2, Wendy M Ingram2, Jennifer T Kirkpatrick2, Chengcheng Hu3, Matthew P Rausch2, Amelia L Gallitano4.   

Abstract

Thymic cellularity is influenced by a variety of biological and environmental factors, such as age and stress; however, little is known about the molecular genetic mechanisms that regulate this process. Immediate early genes of the Early growth response (Egr) family have critical roles in immune function and response to environmental stress. The transcription factors, Egr1, Egr2 and Egr3, play roles in the thymus and in peripheral T-cell activation. Nab2, which binds Egrs 1, 2, and 3 as a co-regulator of transcription, also regulates peripheral T-cell activation. However, a role for Nab2 in the thymus has not been reported. Using Nab2-deficient (KO) mice we found that male Nab2KO mice have reduced thymus size and decreased numbers of thymocytes, compared with age-matched wildtype (WT) mice. Furthermore, the number of thymocytes in Nab2KO males decreases more rapidly with age. This effect is sex-dependent as female Nab2KO mice show neither reduced thymocyte numbers nor accelerated thymocyte loss with age, compared to female WT littermates. Since stress induces expression of Nab2 and the Egrs, we examined whether loss of Nab2 alters stress-induced decrease in thymic cellularity. Restraint stress induced a significant decrease in thymic cellularity in Nab2KO and WT mice, with significant changes in the thymocyte subset populations only in the Nab2KO mice. Stress reduced the percentage of DP cells by half and increased the percentage of CD4SP and CD8SP cells by roughly three-fold in Nab2KO mice. These findings indicate a requirement for Nab2 in maintaining thymocyte number in male mice with age and in response to stress.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Aging; Early growth response gene; Immediate early gene; NGFI-A binding protein; Stress; Thymus

Mesh:

Substances:

Year:  2017        PMID: 28282643      PMCID: PMC5393455          DOI: 10.1016/j.molimm.2017.02.019

Source DB:  PubMed          Journal:  Mol Immunol        ISSN: 0161-5890            Impact factor:   4.407


  68 in total

1.  EGR1, EGR2, and EGR3 activate the expression of their coregulator NAB2 establishing a negative feedback loop in cells of neuroectodermal and epithelial origin.

Authors:  Joerg Kumbrink; Kathrin H Kirsch; Judith P Johnson
Journal:  J Cell Biochem       Date:  2010-09-01       Impact factor: 4.429

Review 2.  Normal structure, function and histology of the thymus.

Authors:  Gail Pearse
Journal:  Toxicol Pathol       Date:  2006       Impact factor: 1.902

3.  Epigenetic programming of stress responses through variations in maternal care.

Authors:  Eric W Fish; Dara Shahrokh; Rose Bagot; Christian Caldji; Timothy Bredy; Moshe Szyf; Michael J Meaney
Journal:  Ann N Y Acad Sci       Date:  2004-12       Impact factor: 5.691

4.  Restraint stress-induced thymic involution and cell apoptosis are dependent on endogenous glucocorticoids.

Authors:  N Tarcic; H Ovadia; D W Weiss; J Weidenfeld
Journal:  J Neuroimmunol       Date:  1998-02       Impact factor: 3.478

5.  Postnatal handling increases the expression of cAMP-inducible transcription factors in the rat hippocampus: the effects of thyroid hormones and serotonin.

Authors:  M J Meaney; J Diorio; D Francis; S Weaver; J Yau; K Chapman; J R Seckl
Journal:  J Neurosci       Date:  2000-05-15       Impact factor: 6.167

6.  The MAPK pathway and Egr-1 mediate stress-related behavioral effects of glucocorticoids.

Authors:  Jean-Michel Revest; Francesco Di Blasi; Pierre Kitchener; Françoise Rougé-Pont; Aline Desmedt; Marc Turiault; François Tronche; Pier Vincenzo Piazza
Journal:  Nat Neurosci       Date:  2005-04-17       Impact factor: 24.884

7.  Killing of immature CD4+ CD8+ thymocytes in vivo by anti-CD3 or 5'-(N-ethyl)-carboxamide adenosine is blocked by glucocorticoid receptor antagonist RU-486.

Authors:  M Jondal; S Okret; D McConkey
Journal:  Eur J Immunol       Date:  1993-06       Impact factor: 5.532

8.  Novel mutants of NAB corepressors enhance activation by Egr transactivators.

Authors:  J Svaren; B R Sevetson; T Golda; J J Stanton; A H Swirnoff; J Milbrandt
Journal:  EMBO J       Date:  1998-10-15       Impact factor: 11.598

9.  Architectural changes in the thymus of aging mice.

Authors:  Danielle Aw; Alberto B Silva; Mandy Maddick; Thomas von Zglinicki; Donald B Palmer
Journal:  Aging Cell       Date:  2008-01-28       Impact factor: 9.304

10.  Differential regulation of NAB corepressor genes in Schwann cells.

Authors:  Rajini Srinivasan; Sung-Wook Jang; Rebecca M Ward; Shrikesh Sachdev; Toshihiko Ezashi; John Svaren
Journal:  BMC Mol Biol       Date:  2007-12-20       Impact factor: 2.946

View more
  2 in total

1.  Immediate Early Genes Anchor a Biological Pathway of Proteins Required for Memory Formation, Long-Term Depression and Risk for Schizophrenia.

Authors:  Ketan K Marballi; Amelia L Gallitano
Journal:  Front Behav Neurosci       Date:  2018-02-19       Impact factor: 3.558

2.  Identification of activity-induced Egr3-dependent genes reveals genes associated with DNA damage response and schizophrenia.

Authors:  Ketan K Marballi; Khaled Alganem; Samuel J Brunwasser; Arhem Barkatullah; Kimberly T Meyers; Janet M Campbell; Annika B Ozols; Robert E Mccullumsmith; Amelia L Gallitano
Journal:  Transl Psychiatry       Date:  2022-08-08       Impact factor: 7.989

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.