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Divergent and dynamic activity of endogenous retroviruses in burn patients and their inflammatory potential.


ABSTRACT: Genes constitute ~3% of the human genome, whereas human endogenous retroviruses (HERVs) represent ~8%. We examined post-burn HERV expression in patients' blood cells, and the inflammatory potentials of the burn-associated HERVs were evaluated. Buffy coat cells, collected at various time points from 11 patients, were screened for the expression of eight HERV families, and we identified their divergent expression profiles depending on patient, HERV, and time point. The population of expressed HERV sequences was patient-specific, suggesting HERVs' inherent genomic polymorphisms and/or differential expression potentials depending on characteristics of patients and courses of injury response. Some HERVs were shared among the patients, while the others were divergent. Interestingly, one burn-associated HERV gag gene from a patient's genome induced IL-6, IL-1?, Ptgs-2, and iNOS. These findings demonstrate that injury stressors initiate divergent HERV responses depending on patient, HERV, and disease course and implicate HERVs as genetic elements contributing to polymorphic injury pathophysiology.

SUBMITTER: Lee KH 

PROVIDER: S-EPMC4104748 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Divergent and dynamic activity of endogenous retroviruses in burn patients and their inflammatory potential.

Lee Kang-Hoon KH   Rah HyungChul H   Green Tajia T   Lee Young-Kwan YK   Lim Debora D   Nemzek Jean J   Wahl Wendy W   Greenhalgh David D   Cho Kiho K  

Experimental and molecular pathology 20140206 2


Genes constitute ~3% of the human genome, whereas human endogenous retroviruses (HERVs) represent ~8%. We examined post-burn HERV expression in patients' blood cells, and the inflammatory potentials of the burn-associated HERVs were evaluated. Buffy coat cells, collected at various time points from 11 patients, were screened for the expression of eight HERV families, and we identified their divergent expression profiles depending on patient, HERV, and time point. The population of expressed HERV  ...[more]

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