» Articles » PMID: 23289855

Injury-elicited Stressors Alter Endogenous Retrovirus Expression in Lymphocytes Depending on Cell Type and Source Lymphoid Organ

Overview
Journal BMC Immunol
Publisher Biomed Central
Date 2013 Jan 8
PMID 23289855
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Murine leukemia virus-type endogenous retroviruses (MuLV-ERVs) constitute ~10% of the mouse genome and are associated with various pathophysiologic processes. In this study, we examined whether MuLV-ERVs' response to burn-elicited stressors is specific for certain lymphocyte populations and/or locations of lymphoid organ.

Results: B- and T-cells, which were sorted from nine lymphoid organs of C57BL/6J mice after burn, were subjected to MuLV-ERV expression analyses. Overall, the post-burn MuLV-ERV expression pattern was dependent on lymphocyte type, time after injury, location of lymphoid organ, and MuLV-ERV type. For instance, the MuLV-ERV expression in T-cells from the thymus and three cervical lymph nodes decreased at 3 hours post-burn while the expression of some MuLV-ERVs was augmented in B-cells derived from the mesenteric lymph node. The MuLV-ERV U3 sequences population of the burn-24 hours group was less diverse in comparison to the no burn and burn-3 hours groups. In addition, it was apparent that at the 24 hours time point, the U3 populations of B-cells from both no burn and burn groups were less heterogeneous than the T-cells' U3 populations. Using the U3 sequences, some of which were isolated only from specific experimental groups (B- vs. T-cells; no burn vs. burn), as probes, 51 putative MuLV-ERVs, including 16 full-length proviruses, were mapped followed by characterization of their biologic properties.

Conclusion: MuLV-ERVs' response to burn-elicited stressors may be differentially controlled depending on lymphocyte type, location of lymphoid organ, MuLV-ERV type, and stress duration.

Citing Articles

Temporal and spatial rearrangements of a repetitive element array on C57BL/6J mouse genome.

Lee K, Yee L, Lim D, Greenhalgh D, Cho K Exp Mol Pathol. 2015; 98(3):439-45.

PMID: 25839092 PMC: 4433582. DOI: 10.1016/j.yexmp.2015.03.037.

References
1.
Volker J, Rameh L, Zhu Q, DeCaprio J, Hansen U . Mitogenic stimulation of resting T cells causes rapid phosphorylation of the transcription factor LSF and increased DNA-binding activity. Genes Dev. 1997; 11(11):1435-46. DOI: 10.1101/gad.11.11.1435. View

2.
Kotadia B, M Ravindranath T, Choudhry M, Haque F, Al-Ghoul W, Sayeed M . Effects of pentoxyfylline on mesenteric lymph node T-cells in a rat model of thermal injury. Shock. 2003; 20(6):517-20. DOI: 10.1097/01.shk.0000098103.41147.54. View

3.
Tomonaga K, Coffin J . Structure and distribution of endogenous nonecotropic murine leukemia viruses in wild mice. J Virol. 1998; 72(10):8289-300. PMC: 110191. DOI: 10.1128/JVI.72.10.8289-8300.1998. View

4.
Hotchkiss R, Tinsley K, Swanson P, Schmieg Jr R, Hui J, Chang K . Sepsis-induced apoptosis causes progressive profound depletion of B and CD4+ T lymphocytes in humans. J Immunol. 2001; 166(11):6952-63. DOI: 10.4049/jimmunol.166.11.6952. View

5.
Lavie L, Kitova M, Maldener E, Meese E, Mayer J . CpG methylation directly regulates transcriptional activity of the human endogenous retrovirus family HERV-K(HML-2). J Virol. 2004; 79(2):876-83. PMC: 538560. DOI: 10.1128/JVI.79.2.876-883.2005. View