Literature DB >> 29973080

Methoxychlor metabolite HPTE alters viability and differentiation of embryonic thymocytes from C57BL/6 mice.

Lucie Leung-Gurung1, Priscilla Escalante Cobb2, Faraj Mourad3, Cristina Zambrano4, Zachary Muscato5, Victoria Sanchez2, Kanya Godde6, Christine Broussard2.   

Abstract

Endocrine-disrupting chemicals (EDC) are widespread in the built and natural environments. Heightened public awareness of their potential danger has led to concern about whether EDC and their metabolites have significant negative biological effects. Studies have shown that EDC like DDT and other organochlorine pesticides, such as methoxychlor (MXC), have adverse effects on immune cells, but no studies have addressed the impact of HPTE, the primary metabolite of MXC. To elucidate the presence and significance of HPTE adverse effects, this study explored the impact of HPTE on a critical window and component of immune system development, embryonic T-cell development. Lesions at this phase of development can lead to lifelong immune dysfunction and increased incidence of immune disease, such as autoimmunity. Embry-onic thymocytes (GD 16-18) from C57BL/6 mice were subjected to an in vitro differentiation culture that mimicked early steps in thymocyte development in the presence of 0.005, 0.05, 0.5, 5, or 50 μM HPTE, or a model endocrine disruptor, DES. The results indicated that compared to the vehicle control, HPTE- and DES-induced death of thymocytes. Annexin-V staining and Caspase 8, markers of programed cell death, revealed that the loss of cells was due at least in part to induction of apoptosis. Moreover, HPTE-induced cell death not only resulted in selective loss of double positive thymocytes, but also loss of developing CD4 intermediate cells (post-double positive partially differentiated thymocyte population). Phenotypic analysis of thymocyte maturation (T-cell receptor, TCR) and TCR ligation (CD5) surface markers revealed that surviving embryonic thymocytes expressed low levels of both. Taken together these data demonstrate that immature embryonic thymocytes are sensitive to HPTE exposure and that HPTE exposure targets thymocyte populations undergoing critical differentiation steps. These findings suggest HPTE may play a pivotal role in MXC exposure-induced immune dysfunction.

Entities:  

Keywords:  CD5; HPTE; Methoxychlor; T-cell development; apoptosis; embryonic development; embryonic thymocyte; endocrine disruptor; thymocyte differentiation

Mesh:

Substances:

Year:  2018        PMID: 29973080      PMCID: PMC6120686          DOI: 10.1080/1547691X.2018.1474978

Source DB:  PubMed          Journal:  J Immunotoxicol        ISSN: 1547-691X            Impact factor:   3.000


  89 in total

1.  The role of the Fas/Fas ligand system in estrogen-induced thymic alteration.

Authors:  G Mor; A Muñoz; R Redlinger; I Silva; J Song; C Lim; F Kohen
Journal:  Am J Reprod Immunol       Date:  2001-10       Impact factor: 3.886

2.  Modulation of immune response following dietary genistein exposure in F0 and F1 generations of C57BL/6 mice: evidence of thymic regulation.

Authors:  T L Guo; R P Chi; X L Zhang; D L Musgrove; C Weis; D R Germolec; K L White
Journal:  Food Chem Toxicol       Date:  2005-09-12       Impact factor: 6.023

3.  Early TCR expression and aberrant T cell development in mice with endogenous prerearranged T cell receptor genes.

Authors:  Thomas Serwold; Konrad Hochedlinger; Matthew A Inlay; Rudolf Jaenisch; Irving L Weissman
Journal:  J Immunol       Date:  2007-07-15       Impact factor: 5.422

4.  Diethylstilbestrol exposure during fetal development affects thymus: studies in fourteen-month-old mice.

Authors:  J B Fenaux; R M Gogal; S Ansar Ahmed
Journal:  J Reprod Immunol       Date:  2004-12       Impact factor: 4.054

5.  T-cell co-stimulation through the CD2 and CD28 co-receptors induces distinct signalling responses.

Authors:  Sigrid S Skånland; Kristine Moltu; Torunn Berge; Einar M Aandahl; Kjetil Taskén
Journal:  Biochem J       Date:  2014-06-15       Impact factor: 3.857

6.  Studies on the in vivo and in vitro estrogenic activities of methoxychlor and its metabolites. Role of hepatic mono-oxygenase in methoxychlor activation.

Authors:  W H Bulger; R M Muccitelli; D Kupfer
Journal:  Biochem Pharmacol       Date:  1978       Impact factor: 5.858

7.  Estrogen receptor alpha is necessary in thymic development and estradiol-induced thymic alterations.

Authors:  J E Staples; T A Gasiewicz; N C Fiore; D B Lubahn; K S Korach; A E Silverstone
Journal:  J Immunol       Date:  1999-10-15       Impact factor: 5.422

8.  Induction of the hepatic CYP2B and CYP3A enzymes by the proestrogenic pesticide methoxychlor and by DDT in the rat. Effects on methoxychlor metabolism.

Authors:  H C Li; S S Dehal; D Kupfer
Journal:  J Biochem Toxicol       Date:  1995-02

9.  A comparison of the estrogenic potencies of estradiol, ethynylestradiol, diethylstilbestrol, nonylphenol and methoxychlor in vivo and in vitro.

Authors:  Leroy C Folmar; Michael J Hemmer; Nancy D Denslow; Kevin Kroll; Jian Chen; Ann Cheek; Harold Richman; Hillary Meredith; E Gordon Grau
Journal:  Aquat Toxicol       Date:  2002-10-02       Impact factor: 4.964

10.  Overexpression of the anti-apoptotic oncogene, bcl-2, in the thymus does not prevent thymic atrophy induced by estradiol or 2,3,7, 8-tetrachlorodibenzo-p-dioxin.

Authors:  J E Staples; N C Fiore; D E Frazier; T A Gasiewicz; A E Silverstone
Journal:  Toxicol Appl Pharmacol       Date:  1998-07       Impact factor: 4.219

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.